- Open Access
Robustness analysis on interspecies interaction network for iron and glucose competition between Candida albicans and zebrafish during infection
BMC Systems Biology volume 8, Article number: S6 (2014)
Candida albicans has emerged as an important model organism for the study of infectious disease. Using high-throughput simultaneously quantified time-course transcriptomics, this study constructed host-pathogen interspecies interaction networks between C. albicans and zebrafish during the adhesion, invasion, and damage stages. Given that iron and glucose have been identified as crucial resources required during the infection process between C. albicans and zebrafish, we focused on the construction of the interspecies networks associated with them. Furthermore, a randomization technique was proposed to identify differentially regulated proteins that are statistically eminent for the three infection stages. The behaviors of the highly connected or differentially regulated proteins identified from the resulting networks were further investigated.
"Robustness" is an important system property that measures the ability of the system tolerating the intrinsic perturbations in a dynamic network. This characteristic provides a systematic and quantitative view to elucidate the dynamics of iron and glucose competition in terms of the interspecies interaction networks. Here, we further estimated the robustness of our constructed interspecies interaction networks for the three infection stages.
The constructed networks and robustness analysis provided significant insight into dynamic interactions related to iron and glucose competition during infection and enabled us to quantify the system's intrinsic perturbation tolerance ability during iron and glucose competition throughout the three infection stages. Moreover, the networks also assist in elucidating the offensive and defensive mechanisms of C. albicans and zebrafish during their competition for iron and glucose. Our proposed method can be easily extended to identify other such networks involved in the competition for essential resources during infection.
According to the World Health Organization, infectious disease remains the leading cause of death for the youth worldwide and people living in low-income countries . As one of the most commonly found commensal and opportunistic fungal pathogens in humans, Candida albicans has become an important model organism for the study of infectious disease. Many factors such as adherence, morphological changes, and secreting hydrolytic enzymes have been shown to be important virulence factors and are linked to the pathogenesis of C. albicans [2, 3]. As a result, understanding the complicated and intertwined mechanisms of C. albicans pathogenesis and its interaction with the host has emerged as an important area of study.
The use of zebrafish as model host in studies of infectious diseases caused by bacteria or viruses is increasing. The genetics, anatomical structure, and physiology of zebrafish are similar to those of mammals, yet their reproductive rate is much higher and the species requires relatively low maintenance costs . In addition, zebrafish has both innate and adaptive immune functions, making them particularly suitable as a model organism for investigating infection [4–6].
"Robustness" is an important system property that measures the ability of the system tolerating the intrinsic perturbations in a dynamic network . In any system, perturbation and uncertainty are inevitable and may render the system unstable. The robustness of a system has become an important topic of interest in industrial design since 1970s . In a biological system, such uncertainty may arise from the intrinsic perturbation of living organisms often caused by mutation, thermal fluctuation and other process noise . These intrinsic perturbations might render the living organisms physiology mechanisms uncoordinated such as metabolic imbalance, hypothermia or cytopathogenesis and death eventually. Therefore, robustness, the ability for living organisms to maintain against intrinsic perturbations, is viewed as a key property for a biological system .
This study aims to understand the complicated offensive and defensive mechanisms of C. albicans and zebrafish during the infection process by constructing interspecies interaction networks between the pathogen and the host, as well as the estimation of the robustness of the networks through the quantified time-course transcriptomics. In our previous report , we constructed the entire interspecies protein interaction network between C. albicans and zebrafish. Here, instead, we focused on the construction of interspecies interaction networks that are associated with iron and glucose, two of the most crucial resources that are competed for during the infection of zebrafish by C. albicans. We further constructed the iron- and glucose competition interspecies networks for three infection stages, i.e., the adhesion, invasion, and damage stages. Proteins that were highly connected or differentially regulated among different infection stages for both the iron and glucose interaction networks were also identified. Finally, we estimated the robustness of each interspecies network that helps us elucidate the dynamics of iron and glucose competition during the infection process. These analyses provided insight into the dynamic behaviors of resource competition between C. albicans and zebrafish and highlighted significant proteins that may play important roles during infection. Based on the developed networks, we were able to quantify the progression of iron and glucose competition throughout the three infection stages. Furthermore, the constructed interspecies networks with robustness estimation help elucidate the offensive and defensive mechanisms of C. albicans and zebrafish during their competition for iron and glucose.
In-depth understanding of the dynamic host-pathogen interspecies interaction networks of the pathogen during infection is essential in the development of new anti-fungal drugs and the improvement of corresponding medical therapy. Our proposed method and in silico experiments could lay the foundation for the development of new therapeutic strategies against infectious diseases.
Materials and methods
Overview of construction of host-pathogen interspecies interaction networks
Our method for the construction of host-pathogen interspecies interaction networks included three major steps: (i) data selection, (ii) protein pools selection, and (iii) construction of networks. The proposed interspecies interaction network construction is shown in Figure 1. To study the competition for iron and glucose between C. albicans and zebrafish during infection, we first selected suitable protein pools for C. albicans and zebrafish that were associated with these important resources. Putative interspecies interaction networks were then identified based on known protein-protein interactions (PPIs) from existing databases, our proposed dynamic model for indirect interspecies interactions between the two organisms, and simultaneously quantified microarray data for C. albicans and zebrafish during infection. Significant interspecies protein interactions between C. albicans and zebrafish among these candidates were identified by removing false-positive interactions using model order selection techniques. Statistically significant proteins were furthermore obtained by comparison of the developed network with networks constructed using microarray data of zebrafish target proteins randomized across time-points.
Dataset mining and integration
Four types of data were used in our method: (i) gene ontology annotation information, (ii) simultaneously quantified time-course microarray gene expression data, (iii) protein-protein interaction data from zebrafish, and (iv) ortholog data between zebrafish and H. sapiens. Annotations for C. albicans and zebrafish proteins were obtained from the Gene Ontology (GO) database (http://www.geneontology.org/) . This database was used to select the C. albicans and zebrafish protein pools as described in the following section (protein pools selection). Genome-wide simultaneously quantified microarray data were obtained from the GEO database (GSE32119). Experiments were performed to obtain in vivo genome-wide simultaneously quantified time-course gene expression profiles for both C. albicans and zebrafish during C. albicans infection of zebrafish. Wild-type zebrafish were injected with C. albicans cells and gene expressions for both C. albicans and zebrafish were monitored at nine time-points (0.5, 1, 2, 4, 6, 8, 12, 16, and 18 hours post-injection [hpi]) using three replicates. Based on histological analysis by Chen et al. , we also divided the microarray data from nine time-points into three overlapping stages (adhesion stage: 0.5, 1, 2, 4 hpi; invasion stage: 2, 4, 6, 8, 12 hpi; damage stage: 6, 8, 12, 16, 18 hpi) for both C. albicans and zebrafish. Ortholog data between zebrafish and H. sapiens were obtained from the InParanoid database (http://inparanoid.sbc.su.se/) . These data were also essential for selecting the zebrafish protein pools. Protein-protein interaction data of H. sapiens were extracted from the Biological General Repository for Interaction Datasets (BioGRID; http://thebiogrid.org/) .
Protein pools selection
In this study, we focused on the construction of interspecies protein interaction networks that were associated with iron and glucose to investigate the competition between C. albicans and zebrafish for these important resources during infection. As a result, our target protein pools were selected via a function-based selection method. For C. albicans, the proteins that were associated with both GO terms of virulence and iron were selected and defined as the iron-related virulence protein pool, while those associated with GO terms of virulence and glucose were defined as the glucose-related virulence protein pool. The corresponding target protein pools for zebrafish were similarly defined as the iron-related and glucose-related immune protein pools. Since few annotations were available for zebrafish, functional annotations for H. sapiens proteins were used to infer possible functional annotations of zebrafish with the help of ortholog data; i.e., if a H. sapiens protein was associated with immunity and had an orthologous protein in zebrafish, we inferred that the zebrafish protein was also immune-related.
For those C. albicans and zebrafish proteins that were selected based on functional annotations, one-way analysis of variance (ANOVA) was applied on the gene expression profiles in our time-course microarray data that correspond to these proteins to further select differentially expressed proteins. The null hypothesis of ANOVA assumed that the average expression level of a gene would be the same at every time point. Proteins from these pools were excluded if the corresponding p-values were < 0.01. The selected protein pools are shown in Table 1 and were used to construct the iron- and glucose competition interspecies networks.
Construction of the host-pathogen interspecies interaction networks
Interactions between host and pathogen are generally complicated and not easily delineated, making it difficult to identify appropriate stochastic dynamic models to describe them. To determine zebrafish target proteins in this study, we examined potential interactions of C. albicans proteins with zebrafish proteins in the selected protein pools using available PPI information.
Due to extremely low coverage of the zebrafish interactomes, ortholog-based PPI prediction was used to infer the potential PPIs within zebrafish. The PPI data of H. sapiens from BioGRID and the ortholog information among these species from the InParanoid database were used to infer the potential intracellular PPIs as proposed in our previous work . We believe that although such cross-species information can affect our candidate networks, the final constructed networks should be more robust against such inaccuracy since actual time-course transcriptome and dynamic modeling were used to prune this candidate model. Once more PPI information become available for zebrafish, the accuracy of our constructed networks can be further improved.
Note that the networks constructed in this manner are biased since known PPI information is used but we believe that such bias is in fact beneficial for the accuracy of the constructed networks. If no such prior information is used, we have to assume that all nodes (proteins) are potentially interactive with all other nodes (proteins). In this case, we believe that there will be more false-positive interactions than the current methodology.
We also assumed that each target protein in the zebrafish iron-related immune protein pool was potentially affected by all proteins in the C. albicans iron-related virulence protein pool (analogously for glucose-related proteins) since there is no existing prior information available for interspecies interactions. The host-pathogen iron interspecies interaction network and the host-pathogen glucose interspecies interaction network were constructed based on these assumptions.
The dynamic model for the -th zebrafish target protein in the host-pathogen interaction network can be described as:
where represents the protein activity level for the -th zebrafish target protein at time , represents the protein activity level of the - th C. albicans protein that might potentially affect the -th zebrafish target protein, and denotes the corresponding interspecies interaction ability between them. We denote as the number of potentially regulatory proteins from C. albicans, as the number of protein-protein interactions in zebrafish for the -th target protein, as the degradation effect for the -th zebrafish target protein, as the protein activity level for the -th zebrafish protein that can potentially interact with the -th target protein, and as the corresponding interaction ability between them. The basal level is denoted by , and the stochastic noise due to model uncertainty and fluctuation of the microarray data is represented by
Compared with our previously developed dynamic network model for single-species network construction , it should be noted that in addition to the single-species protein-protein interaction captured by the term associated with the interaction ability , interspecies interactions are captured by the term associated with the interaction ability . Indirect interspecies interactions are complicated in nature. To create a tractable model for further analysis, we chose a linear approximation to capture the nonlinear effect in . Since is only used to determine whether the indirect interaction exists and its exact value is never used, such an approximation should provide an initial understanding of an interspecies interaction network. In the Results section, we provide evidence from the literature for the identified proteins obtained from our networks to validate these assumptions and approximations.
Since large-scale proteomic data is still not widely available, we substituted all gene expression profiles for protein activity levels. It was reported that gene expression correlates well with distinct proteins for zebrafish, with several categories of genes as exceptions . The interactive parameters for the proposed dynamic model described above can thus be identified using simultaneously quantified time-course microarray data. For this purpose, equation (1) can be rewritten in regression form as follows:
where denotes the regression vector and denotes the parameter vector for the -th zebrafish target protein, which is to be estimated. We used the cubic spline method to interpolate extra time-points within the simultaneously quantified time-course microarray data to avoid over-fitting in the parameter estimation process. Note that equation (2) for different time-points can further be rearranged as:
Defining the notations and , equation (3) can then be rewritten as:
In the dynamic model of host-pathogen interspecies interaction networks, the basal level should always be greater than or equal to zero since the protein activity level in the simultaneously quantified time-course microarray data is always non-negative. Therefore, the parameter estimation problem becomes a constrained least-square problem:
where We focused only on parameters that represent host-pathogen interspecies interactions, i.e., . After the parameters were identified, Akaike's Information Criterion (AIC) was used to select significant C. albicans- zebrafish interactions . AIC can be expressed mathematically as:
where , denotes the number of estimated parameters and denotes the number of the samples used to estimate the parameters. The AIC includes both the estimated residual error and model complexity in one statistic. The AIC value increases as the number of parameters increases and decreases as the variance of the residual error decreases. Since the variance of the residual error may decrease with increasing number of parameters, minimizing the AIC value captures a tradeoff between estimation accuracy and model complexity. Appropriate model order and significant regulations can be determined by ranking models by increasing AIC. Host-pathogen interspecies interaction networks between C. albicans and zebrafish were constructed based on these criteria. We believe that this is a crucial step that improves the accuracy of our constructed networks significantly since PPI information from BioGRID includes all possible interactions in all conditions. This creates many false-positive interactions that need to be and can be excluded based on the actual time-course transcriptome and AIC model order selection in the current condition.
Identification of differentially regulated proteins via randomization techniques
Based on the host-pathogen interaction network constructed above, we were able to obtain the number of linkages of each target protein in zebrafish and the corresponding interspecies interaction proteins in C. albicans during the three infection stages, identifying important hub proteins in both species (see Additional file 1.xlsx in supplementary file for details). To further identify the target proteins and interspecies interaction proteins that had statistically significant roles during each of the three infection stages, we randomized our simultaneously quantified time-course microarray data with respect to time-points. It should be noted that since zebrafish proteins were set as targets for interspecies interaction, this randomization was only applied to zebrafish and not to C. albicans data. Microarray data of zebrafish target immune proteins in the iron-related and glucose-related pool were each randomized 10,000 times. Interspecies interaction networks were constructed and the number of linkages of each protein recorded in each run, yielding the distribution of the number of linkages for each protein in the three infection stages. A protein was determined to be statistically significant in the corresponding stage if its original number of linkages was located closer to the low-probability area rather than the mean at a significance level of p < 0.05 with Student's t-test. Zebrafish target proteins or C. albicans interspecies interaction proteins were determined to be statistically significant for each of the three infection stages (see Table 2, 3, 4, 5, 6, 7, 8, 9, 10, 11, 12, 13 for the complete lists and Figure 2, 3, 4, 5, 6, 7, 8, 9, 10, 11, 12, 13 for the corresponding heatmap. See Additional file 2.zip for the original heatmap).
Estimation of robustness of interspecies interaction networks
The estimation of robustness follows from that in  and is described briefly below. After constructing the dynamic model of the interspecies protein interaction network, we estimate the network robust based the discrete-time dynamic model. Assume that there are z proteins in an interaction network, we can use the following linear discrete-time dynamic model to approximate the interaction network
where X[t] = [ x1[t] x2[t] ... xz[t] ]T represents the protein activity level with a total of z proteins in the network. And the interaction matrix A represents the interaction of protein with interaction ability αij between protein i and protein j. H is the vector of the basal level of each protein. When the system reaches steady state XS, the discrete-time dynamic model (7) could be rewritten as
X S = AX S + H, or X S = (I-A)-1H (8)
Next, we shift the dynamic system by XS (i.e., X[t] = [t] + XS ). Then, we can subtract (7) from (8) to obtain the shifted dynamic system as follow:
Now we can begin to measure the robustness at the new origin where . When a system suffers from intrinsic perturbations such as thermal fluctuation, gene mutation or any other process noise, such perturbation is represented by adding an additional perturbation in to system (9) to obtain:
Higher value means that the system suffers greater intrinsic perturbation which would affect the stability of the dynamic system. If a system can tolerate larger then we can say that system is more robust. Therefore we define the maximum value, in (10) such that the system is still stable as the "robustness" of the network . According to quadratic stability theory [19, 20], if the perturbative network described in (10) is robustly stable, the following inequality has a positive definite solution P=PT>0:
Since robustness is the intrinsic perturbation tolerance ability with respect to the maintenance of steady state, the system must be stable and (11) should be satisfied. Therefore, the robustness value is found by increasing in (11) such that the inequality in (11) can be satisfied with a positive definite solution P=PT>0 until reaching the maximum.
In this study, we aimed to estimate the robustness for three distinctive infection stages (adhesion, invasion, and damage stage) from iron and glucose interspecies protein interaction networks. Based on simultaneously quantified time-course microarray gene expression data and the procedure described in Figure 1, iron and glucose interspecies protein interaction networks for three infection stages were constructed (see Additional file 3.zip in supplementary file for the complete description of the constructed interspecies networks).
In the adhesion stage, we identified 65 PPIs in zebrafish and 273 interspecies interactions between C. albicans and zebrafish in the iron host-pathogen interspecies interaction network with robustness equal to 0.7274 (Table 14, Figure 14), A negative value of robustness represents an unstable system, and a positive value provides a quantitative measure about how much the systems can endure the intrinsic perturbation. We identified 99 PPIs and 168 interspecies interactions in the glucose network with robustness equal to -0.6306. In the invasion stage, we identified 96 PPIs and 271 interspecies interactions in the iron network with robustness equal to -0.4131 and 76 PPIs and 294 interspecies interactions in the glucose network with robustness equal to 1.8281. In the damage stage, we identified 78 PPIs and 204 interspecies interactions in the iron network and 69 PPIs and 286 interspecies interactions in the glucose network with robustness equal to 0.8301 and -0.088.
Based on the constructed networks, we further identified proteins with statistically significant interactions (p < 0.05) for three distinct infection stages. In the adhesion stage, we identified nine significantly interactive iron-related virulence proteins and four glucose-related virulence proteins in C. albicans, and 10 significantly interactive iron-related immune proteins and three glucose-related immune proteins in zebrafish; in the invasion stage, nine iron-related and nine glucose-related virulence proteins, and 11 iron-related and seven glucose-related immune proteins; and in the damage stage, nine iron-related and four glucose-related virulence proteins, and six iron-related and two glucose-related immune proteins.
We additionally investigated the biological processes and molecular functions of these proteins by data mining the existing literature. Based on literature findings, proteins were further divided into three main categories for each infection stage: significantly interactive proteins with strong evidence, significantly interactive proteins with partial evidence, and those that were not yet known to be involved in the infection process.
The proteins with strong evidence are well known to have direct relationships with the designated infection stage between C. albicans and zebrafish. The results from this category confirm the reliability of our method and validate our proposed model. More details for proteins with strong evidence are listed in the Additional file 4.docx in the supplementary file.
The identified proteins with partial evidence represent proteins that were identified to only have indirect connections with the interactions in the designated infection stage. Proteins from this group can be viewed as predictions from our constructed networks since they may be essential for the host-pathogen interaction during infection for the corresponding infection stage. Furthermore, this group may provide new insights into how the infective process progresses within both the host and pathogen. The unknown group includes proteins that have not yet been identified as influential on infection due to of previously associated findings, but may still play a crucial role in resource competition in host-pathogen interactions.
After investigating the host-pathogen interspecies interaction network in the adhesion stage, we identified 273 and 168 interspecies interactions between C. albicans and zebrafish in iron and glucose competition, respectively.
For the iron competition interspecies network, its robustness was estimated to be 0.7274, which was far lager than the robustness estimated in the glucose competition interspecies network (-0.5306). The robustness value of glucose competition interspecies network is negative since this dynamic system is unstable (or not functional) during the adhesion stage. In other words, this indicates that glucose competition is not essential between C. albicans and zebrafish during the adhesion stage. On the other hand, positive robustness of the iron competition interspecies network indicates that iron competition is active and that the zebrafish iron competition network can resist intrinsic perturbation with a ratio of 0.7274. Compared with the glucose competition interspecies network, we can infer that iron competition is the main focus between C. albicans and zebrafish in the adhesion stage.
We further identified proteins with statistically significant interactions in the adhesion stage, including nine virulence iron-related proteins (GO annotation: adhesion activity - 22.2%, metal ion transport - 11.1%, reductase activity - 11.1%, cellular iron ion homeostasis - 22.2%) and four virulence glucose-related proteins (GO annotation: glucose sensor - 50%, cell adhesion - 25%) in C. albicans and 10 immune iron-related proteins (GO annotation: hematopoiesis-related process - 50%, immune response - 20%, metal ion transport - 20%) and three immune glucose-related proteins (GO annotation: immune response - 66.7%, glucose transport - 33.3%) in zebrafish by their corresponding p-values (Table 2, 3, 4, 5, Figure 2, 3, 4, 5).
Differentially regulated proteins with partial evidence
For the C. albicans iron host-pathogen interspecies interaction network, fre10, tup1, ccc2, and hap43 were identified in the adhesion stage.
Fre10 is reported to be responsible for reductase activity and the encoding of cell surface ferric reductase . Iron uptake from transferrin is reported to be impaired in fre10 mutants . The identification of fre10 in the adhesion stage suggests that C. albicans is also beginning to activate the associated mechanisms necessary to compete for iron resources in the host at this point. Tup1 is a global regulator of morphology and metabolism. It plays a key role not only in iron regulation of ferric reductase and ferrous transport activities, but also in iron-dependent gene regulation . The identification of tup1 suggests that most of the iron-related genes are active in the adhesion stage in order to acquire iron from the host. Hap43 has been shown to be an essential protein for the growth of C. albicans in low-iron environments and also for C. albicans virulence in a mouse model . It is also involved in iron assimilation . The identification of hap43 in the early adhesion stage indicates that C. albicans needs to absorb as much iron as possible at this point, since the iron concentration is relatively low during this initial stage of the infection. Ccc2 also plays a pivotal role in iron acquisition during the adhesion stage. It has been reported that ccc2 may be involved in iron reductase activity . The process for the transition between ferrous and ferric iron often involves the donation and acquisition of electrons, which may cause free radical toxicity inside the cell. To prevent the production of toxic free radicals, ferrous iron is oxidized to ferric iron by multicopper oxidase activity . Mnn2 has been shown to be responsible for high-affinity iron ion transport . Since iron is highly important for the pathogen to continue attacking the host, the related transportation mechanisms must also be activated.
For iron competition in zebrafish during this early adhesion stage, we identified atp7a, glrx5, hmox1, tfr1a, and hpx in the iron host-pathogen interaction network. atp7a has been shown to be involved in copper ion transport . Since ccc2, which is involved in preventing damage by toxic free radicals via its reductase activities , was identified in C. albicans, the identification of atp7a in zebrafish implies that the host also invokes a similar mechanism to prevent the damage caused by the intracellular toxicity of free radicals. The presence of glrx5, a member of the glutaredoxin family, suggests that this family is involved in electron carrier activities . The identification of glrx5 is not surprising, as reductase activity is present in both the adhesion and invasion stage and the process depends on the mobilization of electrons. Hmox1 is reported to redirect heme iron to the extracellular region, thereby lowering the accumulation of intracellular iron . Its identification may therefore explain how C. albicans exploits the iron resource from zebrafish, since the acquisition of extracellular iron is easier than that of intracellular iron. It has also been shown that ndfip1-deficient mice have impaired DMT1 regulation and iron homeostasis . The identification of ndfip1 implies that control of the intracellular iron concentration is also important in the competition for iron. tfr1a, an erythroid-specific isoform of transferrin receptor 1 encoded by chianti (cia), is reported to be essential for iron acquisition by erythrocytes . Its presence implies that this protein may be responsible for iron homeostasis in zebrafish during infection by maintaining the iron concentration. Hpx is also widely reported to be related to heme transport and cellular iron ion homeostasis . In this early adhesion stage, the immune response in the zebrafish must be activated to fight the invasion of C. albicans. The protein jmjd6 has been shown to be involved in the phagocytosis of apoptotic cells and associated immune functions . The identification of this immune-related protein in the adhesion stage from our interspecies network suggests that zebrafish also activate their immune functions to target the pathogen at this stage.
For glucose competition, gpia, hif1ab, and ins were identified. gpia is known to be involved in the humoral immune response , while hif1ab is reported to be a critical link between inflammation and oncogenesis and is responsive to interleukin-1 . The identification of gpia and hif1ab implies that the host has activated its immune functions to eliminate the pathogen during the early adhesion stage.
ins stimulates glucose transport by the nitric oxide/cyclic GMP pathway and plays a pivotal role in the uptake of glucose . It is also related to T cell activation . Its identification suggests that glucose transportation is also crucial for efficient uptake of glucose by zebrafish and that zebrafish activate T cells for defensive mechanisms in the early adhesion stage. We observed that most of these identified glucose-related proteins during the adhesion stage were related to biological processes associated with immunity. This interesting observation suggests that the uptake of glucose may support immune functions.
These constructed interspecies interactions of iron and glucose networks provided some insights into how the host-pathogen interaction proceeds during this early stage of infection. Based on the resulting networks (Figure 15), the main goal of the pathogen in the adhesion stage is to adhere to the host and to begin to detect iron and glucose surrounding the attachment site. At the same time, the host activates the immune response to defend against the pathogen, and the biological processes necessary for the production of essential resources are also implemented. In addition, the biological process of metal ion transport is simultaneously activated in both host and pathogen. This suggests that free ions and associated nutrients begin to flow between zebrafish and C. albicans due to the latter's adherence. Following this metal ion transport process, cellular iron ion homeostasis in C. albicans and the hematopoiesis-related process in zebrafish are also activated to maintain the concentration of cellular free ions.
In our constructed host-pathogen interspecies interaction network, we identified 271 and 294 interspecies interactions between C. albicans and zebrafish in the iron and glucose competition, respectively.
For the iron competition interspecies network, its robustness was estimated to be -0.4131, which was far smaller than the robustness estimated in the glucose competition interspecies network (1.8281). We observed that robustness in the iron competition interspecies network changes from 0.7274 to -0.4131 in the adhesion and invasion stage, respectively. This indicates that iron competition is not the main focus during the invasion stage. On the other hand, positive robustness of the glucose competition interspecies network indicates that glucose competition is active and that the zebrafish glucose competition network can resist intrinsic perturbation with a ratio of 1.8281 between C. albicans and zebrafish and during the invasion stage. Compared with the iron competition network, we can infer that glucose competition is the main focus between C. albicans and zebrafish in the invasion stage.
We further identified proteins of statistically significant interactivity in C. albicans during the invasion stage, comprising nine virulence iron-related proteins (GO annotation: hyphal formation - 22.2%, filamentous growth - 22.2%, cellular iron ion homeostasis - 22.2%) and seven virulence glucose-related proteins (GO annotation: hyphal formation - 28.6%, glucose transportation - 14.2%, morphological transition - 14.2%). Among these proteins, most were related to filamentous development and hyphae formation. This is not surprising given that non-filamentous C. albicans mutants are avirulent . In zebrafish, we identified 11 iron-related immune proteins (GO annotation: hematopoiesis-related process - 45.5%, metal ion transport - 9%, immune response - 18.1%) and seven glucose-related immune proteins (GO annotation: immune response - 71.4%) as significant (Table 6, 7, 8, 9, Figure 6, 7, 8, 9).
Differentially regulated proteins with partial evidence
In C. albicans, we identified hmx1, tup1, tpk1, and ftr1 from the iron host-pathogen interspecies interaction network in the invasion stage. Hmx1 is related to cellular iron ion homeostasis. In the hemoglobin uptake and degradation system, hmx1 encodes an active hemoxygenase that degrades hemoglobin to -biliverdin . In our network, hmx1 was identified as being most active in the invasion stage, indicating that hemoglobin degradation occurs mainly during the invasion stage. Moreover, hmx1 is positively regulated by iron deprivation . This could imply that C. albicans acquires iron from iron-binding proteins within the host during the adhesion stage. The main resource that C. albicans competes for upon entering the host is glucose, which enhances hyphae formation. As a result, proteins involved in maintaining the concentration of cellular iron ions are necessary for the invasion stage, which explains the identification of hmx1 in network at this stage. tup1 is known to be a negative regulator of filamentous growth . This is interesting given that C. albicans was thought to initiate hyphae formation and filamentous growth during the invasion stage to enter the host organism. Note that the host-pathogen interaction network we constructed is a dynamically evolving system. Every protein may potentially play two or more roles in the dynamic system, suggesting that tup1 may play roles other than the one discussed above.
tpk1 was shown to be involved in activating downstream transcriptional regulators, including the global regulator efg1. Interestingly, efg1 was also identified in our network during the invasion stage. This suggests that the repression of the protein kinase A subunit tpk1 activates efg1 to support hyphae formation . Ftr1 is a high-iron affinity permease that is involved in iron ion transport. Its deletion prevents systemic infection in mice, and mutant fungi exhibit severe growth defects in low-iron medium .
The gene rim20 was identified as involved in glucose competition. Indeed, several findings indicate that the rim101 transduction pathway regulates C. albicans virulence [46, 47]. The identification of rim20 in our glucose host-pathogen interspecies interaction network in the invasion stage thus indicates that rim20 is pivotal in morphological transition and hyphal formation. Further experimental studies should be performed to verify its specific role in infection.
In zebrafish, we identified slc25a37, slc40a1, and ndfip1 from the iron host-pathogen interspecies interaction network in the invasion stage.
slc25a37 is reported to be associated with hemopoiesis . The appearance of this protein in the invasion stage may suggest that, due to the adherence and invasion of C. albicans, the host requires more iron and oxygen for hyperemia at the attachment site. Slc40a1 is important in the hemoglobin biosynthesis process [49, 50]. The identification of both slc25a37 and slc40a1 implies that the host counters the loss of iron resources due to pathogen invasion by producing more iron. In the invasion stage, we can further infer that C. albicans begins the utilization and transportation of iron while the zebrafish activates relevant heme biosynthesis and red blood cell-producing processes to maintain the balance of all essential cellular elements.
Focusing on glucose-related proteins, dbh, gpia, hif1ab, onecutl, and thbs1 were identified. It has been shown that a deficiency in dopamine beta-hydroxylase (dbh) leads to impaired cellular immunity . The identification of this protein may suggest that immune-related functions are continuously implemented by zebrafish to combat the pathogen in the invasion stage. Onecutl is known to be involved in B cell differentiation . Furthermore, hepatocyte nuclear factor-6 (HNF-6), the prototype onecut family, controls B lymphopoiesis in the fetal liver . The identification of this protein implies that adaptive immunity in zebrafish is activated in the invasion stage. Thrombospondin-1 (thbs1) plays an important role in rheumatoid arthritis and it is also reported to be a pro-inflammatory molecule . Its identification in the invasion stage suggests that the host is infected by the pathogen and needs to activate inflammatory responses to recruit immune cells for defense.
In contrast to the adhesion stage, during the invasion stage the main aim of C. albicans is to form hyphae and to penetrate the host (Figure 16). However, the competition for resources continues, and C. albicans appears to have the advantage in the competition in this middle stage due to the damage done to the host epithelial surface during the adhesion stage. At this stage, the host also enhances associated hematopoietic biological processes to keep iron and glucose resources balanced and stable. In further contrast to the previous adhesion stage, filamentous growth and hyphal formation now begin to flourish. The biological processes of metal ion transport for both host and pathogen continue, allowing both to compete for the associated resources. Notably, the immune response of zebrafish is strongly related to the glucose-related proteins. This may suggest that glucose is an important source of energy for the host in activating immune response mechanisms.
We identified 204 and 286 interspecies interactions between C. albicans and zebrafish in iron and glucose competition, respectively.
For the iron competition interspecies network in the damage stage, its robustness was estimated to be 0.8301, which was far larger than the robustness estimated in the glucose competition interspecies network (-0.088). We observed that robustness in the glucose competition interspecies network changes from 1.8281 to -0.0880 in the invasion and damage stage, respectively. This indicates that the glucose dynamic system is unstable and in fact out of control during the damage stage. This may result from the fact that zebrafish PPI networks are severely damaged and normal glucose metabolism is not possible. Interestingly, positive robustness of the iron competition interspecies network indicates that iron competition is still active and that the zebrafish iron competition network can resist intrinsic perturbation with a ratio of 0.8301.
We further identified proteins of statistically significant interactivity in C. albicans for the damage stage, comprising nine iron-related virulence proteins (GO annotation: pathogenesis and virulence - 33.3%, hyphal formation - 22.2%, filamentous growth - 11%, metal ion transport - 22.2%) and four glucose-related virulence proteins (GO annotation: hyphal growth - 25%, virulence - 50%) (Table 10, 11, Figure 10, 11). According to the GO annotations, most of these proteins are involved in biological processes related to pathogenesis and filamentous growth. This observation indicates that C. albicans begins to increase the destruction of the attachment location and of the entire host organism.
In zebrafish, we identified six iron-related immune proteins (GO annotation: hematopoiesis-related process - 66.7%, immune response - 33.3%) and two glucose-related immune proteins (GO annotation: glucose transport - 50%) (Table 12-13 Figure 12-13). In comparison to the proteins identified in the adhesion and invasion stages, we found many proteins common to the three infection stages, in particular, alas1, hamp1, jmjd6, and tfr1a, which have been widely shown to be involved in hemopoietic activities. This observation suggests that the host continues sanguification in order to compensate for the loss of iron during the infection.
Differentially regulated proteins with partial evidence
Tup1 was again identified during the damage stage in our host-pathogen interspecies interaction network. This may imply that tup1 plays a key role throughout the infection. In the damage stage, tup1 should be responsible for hyphae formation. It was also shown that tup1 mutation results in pseudo-hyphal morphology . The other identified protein, phr2, is reported to be essential for systemic infection of mice in low pH environments only . Specifically, phr2 was undetectable at high pH levels in the blood of mice, while it can be detected at pH < 5.5. Its identification in the damage stage suggests that in order to support its own survival and pathogenesis, C. albicans needs to absorb more iron from the host, in addition to utilizing the reductase pathway to acquire more iron. This creates an environment that is acidic, leading to the activation of phr2. Hap43 is reported to be involved in C. albicans virulence. The deletion of hap43 attenuates the virulence of C. albicans in a mouse model . Its identification suggests that the virulence of C. albicans is enhanced during the damage stage. The fact that ftr2 is active in the damage stage may be due to the higher level of iron availability . In this stage, the iron competition between host and pathogen ceases. C. albicans appears to be victorious in the competition for this essential resource, resulting in greater availability of iron for C. albicans than during the previous two stages.
In zebrafish, only edn1 was identified in the glucose interspecies interaction network in the damage stage. Endothelin-1 (edn1) is reported to be capable of stimulating glucose transport in the target tissues of insulin . Its presence suggests that although the zebrafish may eventually succumb to the infection, glucose as a fundamental element for maintaining life is still needed by the host.
During the damage stage (Figure 17), the pathogen strengthens its pathogenic attack by inducing filamentous growth. The transportation of iron continues. Although the host appears to have no other strategies to defend against the invader, it however still maintains the production of essential resources to prolong its own survival.
From the engagement in the previous two stages, C. albicans successfully infects the zebrafish and continues to damage the host. However, while the zebrafish's system is now much weaker, it still seeks to remain viable by continuing the hematopoiesis process (a fundamental process for any biological organism).
The above observations and predictions derived from the constructed host-pathogen interspecies interaction networks allowed us to explore the dynamics and underlying mechanisms by which C. albicans interacts with zebrafish during infection, providing new insights for future experiments in infectious diseases.
During infection, the competition for iron and glucose plays a critical role in the battle between host and pathogen. Our estimation of robustness of the competition interspecies networks between C. albicans and zebrafish assists in elucidating the offensive and defensive mechanisms adopted by both organisms.
C. albicans, as an aggressor
The strategies of C. albicans for the competition for iron have evolved to high efficiency. These strategies can be related to three crucial iron acquisition sub-systems: (i) siderophore uptake, (ii) hemoglobin degradation, and (iii) a reductive pathway system. We can also use the estimation of the robustness to observe the relationship between three infection stages from a systematic point-of-view to discover the focus of resource competition as an offensive strategy for C. albicans.
In the early adhesion stage, robustness for the iron interspecies competition network is 0.7274. Compared with the robustness of the unstable glucose interspecies competition network (-0.5306), iron interspecies competition network is more robust to withstand the intrinsic perturbation such as thermal fluctuation or other process noise. This indicates that C. albicans conducts systematic iron collection during the early adhesion stage. During the adhesion stage, the primary goal of C. albicans is to adhere to the epithelial cell surface of the host tissue. Among the proteins that were identified in our iron host-pathogen interspecies interaction networks, tup1 and asc1 were related to attachment [57, 58]. C. albicans seems to begin to detect the iron in its surroundings at this stage. These iron resources, however, are often in the form of ferric iron (Fe3+) in the host organism rather than the soluble ferrous form (Fe2+). C. albicans cannot use ferric iron directly, and its activation of the reductive pathway system is necessary to reduce ferric iron to the ferrous form. This activation can be inferred from the network during the adhesion stage, where the protein fre10 (previously reported to be highly related to the reductive activity ) was identified. The reductive pathway system is also involved in multicopper oxidase activity, which prevents the production of toxic free radicals from the reductive process during the transition of electrons by oxidizing ferrous iron to ferric iron. We also identified the copper transporter ccc2, which is known to be involved in multicopper oxidase activity . Aside from acquiring hemoglobin from its surroundings, it is also necessary for C. albicans to activate the relevant receptors. The well-known ferritin receptor, als3, was also identified but was found to be much more active in the damage stage than the adhesion stage. This may suggest that the acquisition of ferritin occurs mainly during the latter stage since ferritin is more stable than other types of iron proteins . Further investigation of the numbers of linkages in the adhesion stage (see Additional file 1.xlsx in supplementary file for details) revealed that the hemoglobin-receptor gene family rbt4 had the maximum number of linkages. This may suggest that during early infection, the initial strategy of C. albicans is to activate all receptors involved in the detection of ferritin, transferrin, and hemoglobin, to detect possible sources of iron in its surroundings. If ferric iron is found to be the major iron resource available, the reductive pathway system is then activated to convert ferric iron to the usable ferrous form. It can be inferred from the network that C. albicans is mainly involved in adherence and detection of the iron sources in its surroundings during the adhesion stage, preparing the pathogen for the following invasion and damage stage. Similar to iron detection, C. albicans also begins sensing for glucose for possible uptake. Hgt4 and gpa2 were identified in our glucose network as involved in glucose detection [21, 22]. Furthermore, snf1 was identified as involved in cell adhesion . The identification of this glucose-related protein suggests that glucose is also an essential resource for adhesion activity in C. albicans.
In the next stage of the infection process, normally known as the invasion stage, the robustness value of the iron competition interspecies network is negative (-0.4143) while it is positive in the glucose competition interspecies network (1.8281). This demonstrates that the competition for glucose might be more important than iron during the invasion stage. When invasion starts, C. albicans simultaneously begins hyphal formation and filamentous growth, penetrating the host tissue. From our constructed glucose interspecies network, the protein hgt4, tps1, gpa2, and rim20 were identified to be involved in hyphal formation and virulence. Since hyphal transition is the main focus for C. albicans at this stage, these glucose-related proteins are needed to support its development. The positive value of the robustness for the glucose competition network (1.8281) indicates that C. albicans needs stable growth of mycelium by preying glucose from zebrafish. And it infers the glucose is the main target and more relevant during the invasion stage. On the other hand, an adequate supply of iron is also necessary for its invasion and survival. Iron obtained via the reductive pathway is often bound to the high-affinity iron permease and then transported into the cell of the pathogen for further utilization or storage. The protein ftr1 (which is reported to play an important role in this transportation and storage ) was identified in the iron interspecies interaction network. Efficient use and transportation of iron resources obtained from the adhesion stage are therefore crucial.
In the last (damage) stage of the infection process, iron acquisition by C. albicans is reduced since the iron acquired from the host almost reaches saturation for the pathogen at this point. The positive robustness value (0.8301) of the iron competition interspecies network indicates that C. albicans now stably focuses on the storage of the iron obtained during the first two stages. Compared with iron competition interspecies network, robustness of the glucose competition interspecies network is negative (-0.0880), indicating a unstable system. This suggests that C. albicans focus on iron competition instead of glucose competition in the last damage stage, where zebrafish cells are severely damaged and depriving irons from the damaged zebrafish cells become the primary goal for C. albicans.
As the aggressor in the iron and glucose competition, C. albicans was found to execute well-planned strategies, as can be inferred from the significantly interactive proteins identified in the networks. In the early stage of infection, the pathogen mainly focuses on adhering to the epithelial surface of the host and detecting the available iron sources in its surroundings. In the invasion stage, C. albicans begins harvesting glucose to support its filamentous growth and hyphal formation, as well as transporting and storing associated resources from the zebrafish. In the final damage stage, C. albicans enhances its attack to finally overcome the host in this competition for resources.
Zebrafish, as a defender
In the zebrafish host, we identified several proteins (alas2, tfr1a, slc25a37) that are associated with heme synthesis and hematopoiesis in the three constructed host-pathogen interspecies interaction networks throughout the infection. This may imply that heme synthesis and the hematopoiesis process are upregulated during the infection process to inhibit iron deprivation by C. albicans. As reductase activity is involved in both pathogen and host during iron competition, we also identified glrx5 (reported to be responsible for the mobilization of electrons ) in both the adhesion and invasion stage. When the pathogen adheres to the surface of the host cell, the relevant pattern recognition receptors in zebrafish are induced to produce the precise antimicrobial peptides required to defend against the pathogen. In our adhesion stage networks, hamp1 was identified as being involved in this process .
In the invasion and damage stage, the zebrafish attempts to produce more iron to counteract the iron deprivation induced by C. albicans. Accordingly, several proteins associated with hematopoiesis (alas2, hamp1, slc40a1, slc25a37, tfr1a, and hpx) were also identified. Interestingly, robustness analysis for the two stages reveal that iron competition interspecies networks are unstable during the invasion stage but stable during the damage stage. This could infer that the activities associated with hematopoiesis are stronger during the damage stage since zebrafish is now severely damaged.
In investigating significantly interactive proteins in zebrafish during the three distinct infection stages, we observed that the zebrafish maintained almost the same biological process of hematopoiesis in order to prolong its life as much as possible.
As a defender in this competition for resources, zebrafish are passive and responsive. Even though the host is losing essential resources, it has no defensive strategies beyond enhancing the production of these resources to keep its own biological processes balanced and stable.
With respect to glucose competition, several identified proteins were associated with immunity (gpia, hif1ab, and ins in the adhesion stage; dbh, gpia, hif1ab, onecutl, and thbs1 in the invasion stage). The identification of these glucose-related immune proteins indicates that in addition to engaging in competition for iron and glucose, zebrafish also activate their immune system to combat the intruder. We observe that the not only the robustness of glucose competition interspecies network in the invasion stage reaches its peak, but also most of immune-related proteins are identified in the invasion stage than in the other two stages. This strongly suggests that the major defense of the host primarily occurred during the middle stage of the infection, when C. albicans initiated hyphal formation and filamentous growth.
Our proposed model provides a novel way to explore and predict how these two organisms interact during infection, employing the construction of host-pathogen interspecies interaction networks and use of simultaneously quantified time-course microarray data. Moreover, the robustness analysis provided a quantitative measure of the intrinsic perturbation tolerance ability of a competition network for each infection stage. This helps elucidate the resource competition mechanisms underlying the infection between C. albicans and zebrafish. We identified several proteins with statistically significant interactions during the three infection stages (adhesion stage: nine iron-related and four glucose-related virulence proteins in C. albicans, 10 iron-related and three glucose-related immune proteins in zebrafish; invasion stage: nine iron-related and seven glucose-related virulence proteins, 11 iron-related and seven glucose-related immune proteins; damage stage: nine iron-related and four glucose-related virulence proteins, six iron-related and two glucose-related immune proteins). Combining these useful tools, we provided insights to elucidate the offensive and defensive mechanisms of C. albicans and zebrafish during their competition for iron and glucose.
World Health Organization (1999) Leading causes of death:
Calderone RA, Fonzi WA: Virulence factors of Candida albicans. Trends Microbiol. 2001, 9: 327-335. 10.1016/S0966-842X(01)02094-7.
Cutler JE: Putative virulence factors of Candida albicans. Annu Rev Microbiol. 1991, 45: 187-218. 10.1146/annurev.mi.45.100191.001155.
Meeker ND, Trede NS: Immunology and zebrafish: spawning new models of human disease. Dev Comp Immunol. 2008, 32: 745-757. 10.1016/j.dci.2007.11.011.
Zon LI, Peterson RT: In vivo drug discovery in the zebrafish. Nat Rev Drug Discov. 2005, 4: 35-44. 10.1038/nrd1606.
Sullivan C, Kim CH: Zebrafish as a model for infectious disease and immune function. Fish Shellfish Immunol. 2008, 25: 341-350. 10.1016/j.fsi.2008.05.005.
Chen BS, Wang YC, Wu WS, Li WH: A new measure of the robustness of biochemical networks. Bioinformatics. 2005, 11: 2698-705.
Manfred M, Evanghelos Z: Robust process control. Introduction. 1989, Englewood Cliffs, Prentice Hall, 4-
Tu CT, Chen BS: New Measurement Methods of Network Robustness and Response Ability via Microarray Data. PLoS One. 2013, 1: e55230-
Stelling J, Sauer U, Szallasi Z, Doyle FJ, Doyle J: Robustness of cellular functions. Cell. 2004, 118: 675-685. 10.1016/j.cell.2004.09.008.
Zong-Yu Kuo YJC, Chun-Cheih Chao, Fu-Chen Liu, Chung-Yu Lan, Bor-Sen Chen: Identification of Infection- and Defense-Related Genes via a Dynamic Host-Pathogen Interaction Network Using a Candida Albicans -Zebrafish Infection Model. Joural of Innate Immunity. 2013
Ashburner M, Ball CA, Blake JA, Botstein D, Butler H, et al: Gene ontology: tool for the unification of biology. The Gene Ontology Consortium. Nat Genet. 2000, 25: 25-29. 10.1038/75556.
Yan Yu Chen, Chun-Cheih Chao, Fu-Chen Liu, Po-Chen Hsu, Hsueh-Fen Chen, Shih-Chi Peng, Yung-Jen Chuang, Chung-Yu Lan, Wen-Ping Hsieh, David Shan Hill Wong: Dynamic Transcript Profiling of Candida albicans Infection in Zebrafish: A Pathogen-Host Interaction Study. PLoS ONE. 2013, e72483-
Berglund AC, Sjolund E, Ostlund G, Sonnhammer EL: InParanoid 6: eukaryotic ortholog clusters with inparalogs. Nucleic Acids Res. 2008, 36: D263-266.
Stark C, Breitkreutz BJ, Reguly T, Boucher L, Breitkreutz A, et al: BioGRID: a general repository for interaction datasets. Nucleic Acids Res. 2006, 34: D535-539. 10.1093/nar/gkj109.
Yu-Chao Wang, Che Lin, Ming-Ta Chuang, Wen-Ping Hsieh, Chung-Yu Lan, Yung-Jen Chuang, Bor-Sen Chen: Interspecies protein interaction network construction for characterization of host-pathogen interactions. BMC System. 2013, 7-79.
Magnus Palmblad, Henkel Christiaan V, Dirks Ron P, Meijer Annemarie H, Deelder André M, Spaink Herman P: Parallel deep transcriptome and proteome analysis of zebrafish larvae. BMC Research Notes. 2013, 6-428.
Akaike H: A new look at the statistical model identification. Automatic Control. IEEE Transactions on. 1974, 19: 716-723.
Chen BS, Zhang W: Stochastic H2/H' control with state-dependent noise. IEEE Trans Automatic Control. 2004, 49: 45-57. 10.1109/TAC.2003.821400.
Zhang W, Chen BS: State feedback H' control for a class of nonlinear stochastic systems. SIAM J on Control and Optimization. 2006, 44: 1973-1991. 10.1137/S0363012903423727.
Knight SA, Vilaire G, Lesuisse E, Dancis A: Iron acquisition from transferrin by Candida albicans depends on the reductive pathway. Infect Immun. 2005, 73: 5482-5492. 10.1128/IAI.73.9.5482-5492.2005.
Knight SA, Lesuisse E, Stearman R, Klausner RD, Dancis A: Reductive iron uptake by Candida albicans: role of copper, iron and the TUP1 regulator. Microbiology. 2002, 148: 29-40.
Hsu PC, Yang CY, Lan CY: Candida albicans Hap43 is a repressor induced under low-iron conditions and is essential for iron-responsive transcriptional regulation and virulence. Eukaryot Cell. 2011, 10: 207-225. 10.1128/EC.00158-10.
Homann OR, Dea J, Noble SM, Johnson AD: A phenotypic profile of the Candida albicans regulatory network. PLoS Genet. 2009, 5: e1000783-10.1371/journal.pgen.1000783.
Weissman Z, Shemer R, Kornitzer D: Deletion of the copper transporter CaCCC2 reveals two distinct pathways for iron acquisition in Candida albicans. Molecular Microbiology. 2002, 44: 1551-1560. 10.1046/j.1365-2958.2002.02976.x.
Almeida RS, Wilson D, Hube B: Candida albicans iron acquisition within the host. FEMS Yeast Res. 2009, 9: 1000-1012. 10.1111/j.1567-1364.2009.00570.x. PMID: 19788558
Bai C, Chan FY, Wang Y: Identification and functional characterization of a novel Candida albicans gene CaMNN5 that suppresses the iron-dependent growth defect of Saccharomyces cerevisiae aft1Delta mutant. Biochem J. 2005, 389: 27-35. 10.1042/BJ20050223.
Kaler SG: ATP7A-related copper transport diseases-emerging concepts and future trends. Nat Rev Neurol. 2011, 7: 15-29. 10.1038/nrneurol.2010.180.
Madsen EC, Gitlin JD: Zebrafish mutants calamity and catastrophe define critical pathways of gene-nutrient interactions in developmental copper metabolism. PLoS Genet. 2008, 4: e1000261-10.1371/journal.pgen.1000261.
Foloppe N, Nilsson L: The glutaredoxin -C-P-Y-C- motif: influence of peripheral residues. Structure. 2004, 12: 289-300.
Poss KD, Tonegawa S: Reduced stress defense in heme oxygenase 1-deficient cells. Proc Natl Acad Sci USA. 1997, 94: 10925-10930. 10.1073/pnas.94.20.10925.
Foot NJ, Leong YA, Dorstyn LE, Dalton HE, Ho K, et al: Ndfip1-deficient mice have impaired DMT1 regulation and iron homeostasis. Blood. 2011, 117: 638-646. 10.1182/blood-2010-07-295287.
Wingert RA, Brownlie A, Galloway JL, Dooley K, Fraenkel P, et al: The chianti zebrafish mutant provides a model for erythroid-specific disruption of transferrin receptor 1. Development. 2004, 131: 6225-6235. 10.1242/dev.01540.
Takahashi N, Takahashi Y, Putnam FW: Complete amino acid sequence of human hemopexin, the heme-binding protein of serum. Proc Natl Acad Sci USA. 1985, 82: 73-77. 10.1073/pnas.82.1.73.
Bose J, Gruber AD, Helming L, Schiebe S, Wegener I, et al: The phosphatidylserine receptor has essential functions during embryogenesis but not in apoptotic cell removal. J Biol. 2004, 3: 15-10.1186/jbiol10.
Gurney ME, Apatoff BR, Spear GT, Baumel MJ, Antel JP, et al: Neuroleukin: a lymphokine product of lectin-stimulated T cells. Science. 1986, 234: 574-581. 10.1126/science.3020690.
Jung YJ, Isaacs JS, Lee S, Trepel J, Neckers L: IL-1beta-mediated up-regulation of HIF-1alpha via an NFkappaB/COX-2 pathway identifies HIF-1 as a critical link between inflammation and oncogenesis. FASEB J. 2003, 17: 2115-2117. PMID: 12958148
Bergandi L, Silvagno F, Russo I, Riganti C, Anfossi G, et al: Insulin stimulates glucose transport via nitric oxide/cyclic GMP pathway in human vascular smooth muscle cells. Arterioscler Thromb Vasc Biol. 2003, 23: 2215-2221. 10.1161/01.ATV.0000107028.20478.8e.
Ma H, Ke Y, Li Q, Kapp JA: Bovine and human insulin activate CD8+-autoreactive CTL expressing both type 1 and type 2 cytokines in C57BL/6 mice. J Immunol. 2000, 164: 86-92. 10.4049/jimmunol.164.1.86. 35. Bai C, Chan FY, Wang Y (2005) Identification and functional characterization of a novel Candida albicans gene CaMNN5 that suppresses the iron-dependent growth defect of Saccharomyces cerevisiae aft1Delta mutant. Biochem J 389: 27-35
Lo HJ, Kohler JR, DiDomenico B, Loebenberg D, Cacciapuoti A, et al: Nonfilamentous C. albicans mutants are avirulent. Cell. 1997, 90: 939-949. 10.1016/S0092-8674(00)80358-X.
Pendrak ML, Chao MP, Yan SS, Roberts DD: Heme oxygenase in Candida albicans is regulated by hemoglobin and is necessary for metabolism of exogenous heme and hemoglobin to alpha-biliverdin. J Biol Chem. 2004, 279: 3426-3433.
Santos R, Buisson N, Knight S, Dancis A, Camadro JM, et al: Haemin uptake and use as an iron source by Candida albicans: role of CaHMX1-encoded haem oxygenase. Microbiology. 2003, 149: 579-588. 10.1099/mic.0.26108-0.
Braun BR, Johnson AD: Control of filament formation in Candida albicans by the transcriptional repressor TUP1. Science. 1997, 277: 105-109. 10.1126/science.277.5322.105.
Stichternoth C, Fraund A, Setiadi E, Giasson L, Vecchiarelli A, et al: Sch9 kinase integrates hypoxia and CO2 sensing to suppress hyphal morphogenesis in Candida albicans. Eukaryot Cell. 2011, 10: 502-511. 10.1128/EC.00289-10.
Ramanan N, Wang Y: A high-affinity iron permease essential for Candida albicans virulence. Science. 2000, 288: 1062-1064. 10.1126/science.288.5468.1062.
Yuan X, Mitchell BM, Hua X, Davis DA, Wilhelmus KR: The RIM101 signal transduction pathway regulates Candida albicans virulence during experimental keratomycosis. Invest Ophthalmol Vis Sci. 2010, 51: 4668-4676. 10.1167/iovs.09-4726.
Davis D, Wilson RB, Mitchell AP: RIM101-dependent and-independent pathways govern pH responses in Candida albicans. Mol Cell Biol. 2000, 20: 971-978. 10.1128/MCB.20.3.971-978.2000.
Ransom DG, Haffter P, Odenthal J, Brownlie A, Vogelsang E, et al: Characterization of zebrafish mutants with defects in embryonic hematopoiesis. Development. 1996, 123: 311-319.
Fraenkel PG, Traver D, Donovan A, Zahrieh D, Zon LI: Ferroportin1 is required for normal iron cycling in zebrafish. J Clin Invest. 2005, 115: 1532-1541. 10.1172/JCI23780.
Donovan A, Brownlie A, Dorschner MO, Zhou Y, Pratt SJ, et al: The zebrafish mutant gene chardonnay (cdy) encodes divalent metal transporter 1 (DMT1). Blood. 2002, 100: 4655-4659. 10.1182/blood-2002-04-1169.
Alaniz RC, Thomas SA, Perez-Melgosa M, Mueller K, Farr AG, et al: Dopamine beta-hydroxylase deficiency impairs cellular immunity. Proc Natl Acad Sci USA. 1999, 96: 2274-2278. 10.1073/pnas.96.5.2274.
Bouzin C, Clotman F, Renauld JC, Lemaigre FP, Rousseau GG: The onecut transcription factor hepatocyte nuclear factor-6 controls B lymphopoiesis in fetal liver. J Immunol. 2003, 171: 1297-1303. 10.4049/jimmunol.171.3.1297.
Rico MC, Manns JM, Driban JB, Uknis AB, Kunapuli SP, et al: Thrombospondin-1 and transforming growth factor beta are pro-inflammatory molecules in rheumatoid arthritis. Transl Res. 2008, 152: 95-98. 10.1016/j.trsl.2008.06.002.
Murad AM, Leng P, Straffon M, Wishart J, Macaskill S, et al: NRG1 represses yeast-hypha morphogenesis and hypha-specific gene expression in Candida albicans. EMBO J. 2001, 20: 4742-4752. 10.1093/emboj/20.17.4742.
De Bernardis F, Muhlschlegel FA, Cassone A, Fonzi WA: The pH of the host niche controls gene expression in and virulence of Candida albicans. Infect Immun. 1998, 66: 3317-3325.
Imamura T, Huang J, Dalle S, Ugi S, Usui I, et al: beta -Arrestin-mediated recruitment of the Src family kinase Yes mediates endothelin-1-stimulated glucose transport. J Biol Chem. 2001, 276: 43663-43667. 10.1074/jbc.M105364200.
Villar CC, Kashleva H, Dongari-Bagtzoglou A: Role of Candida albicans polymorphism in interactions with oral epithelial cells. Oral Microbiol Immunol. 2004, 19: 262-269. 10.1111/j.1399-302X.2004.00150.x.
Kim SW, Joo YJ, Kim J: Asc1p, a ribosomal protein, plays a pivotal role in cellular adhesion and virulence in Candida albicans. J Microbiol. 2010, 48: 842-848. 10.1007/s12275-010-0422-1.
Weissman Z, Shemer R, Kornitzer D: Deletion of the copper transporter CaCCC2 reveals two distinct pathways for iron acquisition in Candida albicans. Mol Microbiol. 2002, 44: 1551-1560. 10.1046/j.1365-2958.2002.02976.x.
Almeida RS, Brunke S, Albrecht A, Thewes S, Laue M, et al: The hyphal-associated adhesin and invasin Als3 of Candida albicans mediates iron acquisition from host ferritin. PLoS Pathog. 2008, 4: e1000217-10.1371/journal.ppat.1000217.
Vyas VK, Kuchin S, Berkey CD, Carlson M: Snf1 kinases with different beta-subunit isoforms play distinct roles in regulating haploid invasive growth. Mol Cell Biol. 2003, 23: 1341-1348. 10.1128/MCB.23.4.1341-1348.2003.
Shike H, Shimizu C, Lauth X, Burns JC: Organization and expression analysis of the zebrafish hepcidin gene, an antimicrobial peptide gene conserved among vertebrates. Dev Comp Immunol. 2004, 28: 747-754. 10.1016/j.dci.2003.11.009.
The work was supported by the National Science Council of Taiwan, R.O.C. with funding number: NSC-100-2627-B-007-004, NSC102-2745-E-007-001-ASP, NSC100-2627-B-007-002 and NSC97-2627-B-007-006. The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.
The publication of this supplement was funded by the National Science Council of Taiwan, R.O.C. with funding number: NSC-100-2627-B-007-004.
This article has been published as part of BMC systems Biology Volume 8 Supplement 5, 2014: Proceedings of the 25th International Conference on Genome Informatics (GIW/ISCB-Asia): Systems Biology. The full contents of the supplement are available online at http://www.biomedcentral.com/bmcsystbiol/supplements/8/S5.
The authors declare that they have no competing interests.
Conceived and designed the experiments: YJC CYL. Performed the experiments: YJC CYL. Analyzed the data: CNL CL YCW FYL WPH BSC. Contributed reagents/materials/analysis tools: CL CNL YCW FYL YWC BSC. Wrote the manuscript: CL CNL
Electronic supplementary material
Additional file 1: GO annotations of top 10 hub proteins ranked by degree in glucose and iron PPIN for adhesion, invasion and damage stage. (XLSX 16 KB)
Additional file 3: The glucose and iron protein-protein interaction network (PPIN) for the adhesion, invasion and damage stage. (ZIP 86 KB)
Additional file 4: Differentially regulated proteins with strong evidence in glucose and iron PPIN for adhesion, invasion and damage stage. (DOCX 157 KB)
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Lin, C., Lin, CN., Wang, YC. et al. Robustness analysis on interspecies interaction network for iron and glucose competition between Candida albicans and zebrafish during infection. BMC Syst Biol 8, S6 (2014). https://doi.org/10.1186/1752-0509-8-S5-S6
- Gene Ontology
- Infection Stage
- Filamentous Growth
- Invasion Stage
- Hyphal Formation