Type III secretion system effectors form robust and flexible intracellular virulence networks

doi:10.1126/science.abc9531

GSTDTAP > 气候变化

DOI	10.1126/science.abc9531
	Type III secretion system effectors form robust and flexible intracellular virulence networks
	David Ruano-Gallego; Julia Sanchez-Garrido; Zuzanna Kozik; Elena Núñez-Berrueco; Massiel Cepeda-Molero; Caroline Mullineaux-Sanders; Jasmine Naemi-Baghshomali Clark; Sabrina L. Slater; Naama Wagner; Izabela Glegola-Madejska; Theodoros I. Roumeliotis; Tal Pupko; Luis Ángel Fernández; Alfonso Rodríguez-Patón; Jyoti S. Choudhary; Gad Frankel
	2021-03-12
发表期刊	Science
出版年	2021
英文摘要	Many disease-causing bacteria use a molecular syringe to inject dozens of their proteins, called effectors, into intestinal cells, blocking key immune responses. Ruano-Gallego et al. used the mouse pathogen Citrobacter rodentium to model effector function in vivo. They found that effectors work together as a network, allowing the microbe great flexibility in maintaining pathogenicity. An artificial intelligence platform correctly predicted colonization outcomes of alternative networks from the in vivo data. However, the host was able to bypass the obstacles erected by different effector networks and activate complementary immune responses that cleared the pathogen and induced protective immunity. Science , this issue p. [eabc9531][1] ### INTRODUCTION Infections with many Gram-negative pathogens, including Escherichia coli , Salmonella , Shigella , and Yersinia , rely on the injection of effectors via type III secretion systems (T3SSs). The effectors hijack cellular processes through multiple mechanisms, including molecular mimicry and diverse enzymatic activities. Although in vitro analyses have shown that individual effectors can exhibit complementary, interdependent, or antagonistic relationships, most in vivo studies have focused on the contribution of single effectors to pathogenesis. Citrobacter rodentium is a natural mouse pathogen that shares infection strategies and virulence factors with the human pathogens enteropathogenic and enterohemorrhagic E. coli (EPEC and EHEC). The ability of these pathogens to colonize the gastrointestinal tract is mediated by the injection of effectors via a T3SS. Although C. rodentium infects 31 effectors, the prototype EPEC strain E2348/69 translocates 21 effectors. ### RATIONALE The aim of this study was to test the hypotheses that, rather than operating individually, the T3SS effectors form robust intracellular networks that can sustain large contractions and that expanded effector repertoires play a role in distinct disease phenotypes and host adaption. ### RESULTS We tested the effector-network paradigm by infecting mice with >100 C. rodentium effector mutant combinations. First, using machine learning prediction algorithms, we discovered additional effectors, NleN and NleO. We then sequentially deleted effector genes from two distinct starting points to reach sustainable endpoints, which resulted in strains missing 19 unrelated effectors (CR14) or 10 effectors involved in the modulation of innate immune responses in intestinal epithelial cells (IECs) (CRi9). Moreover, we deleted Map and EspF, which target the mitochondria and disrupt tight junctions. Unexpectedly, all strains colonized the colon and activated conserved metabolic and antimicrobial processes in the IECs while eliciting distinct cytokine and immune cell infiltration responses. In particular, although infection with C. rodentium Δ map /Δ espF failed to induce secretion of interleukin-22 (IL-22), CR14 and CRi9 triggered heightened secretion of IL-6 and granulocyte-macrophage colony-stimulating factor (GM-CSF) and of IL-22, interferon-γ (IFN-γ), and IL-17 from colonic explants, respectively. Nonetheless, infection with CR14 or CRi9 induced protective immunity against secondary infections. Although Tir, EspZ, and NleA are essential, other effectors exhibit context-dependent essentiality in vivo. Moreover, C. rodentium expressing the effector repertoire of EPEC E2348/69 failed to efficiently colonize mice. We used curated functional information and our in vivo data to train a machine learning model that predicted values for colonization efficiency of previously uncharacterized mutant combinations. Notably, a mutant with a low predicted value, lacking only nleF , nleG8 , nleG1 , nleB , and espL , failed to colonize. ### CONCLUSION Our analysis revealed that T3SS effectors form robust networks, which can sustain substantial contractions while maintaining virulence, and that the composition of the effector network contributes to host adaptation. Alternative effector networks within a single pathogen triggered markedly different immune responses yet induced protective immunity. CR14 did not tolerate any further contraction, which suggests that this network reached its robustness limit with only 12 effectors. As the robustness limits of other effector networks depend on the contraction starting point and the order of the deletions, machine learning models could transform our ability to predict alternative network functions. Together, this study demonstrates the robustness of T3SS effector networks and the ability of IECs to withstand drastic perturbations while maintaining antibacterial functions. ![Figure][2] T3SS effectors form robust intracellular networks. T3SS effector networks can sustain substantial contractions while maintaining virulence. Using C. rodentium as a model showed that although triggering the conserved infection signatures in IECs, distinct networks induce divergent immune responses and affect host adaption. Because the robustness limit depends on the contraction sequence, machine learning models could transform our ability to predict the virulence potential of alternative networks. Infections with many Gram-negative pathogens, including Escherichia coli , Salmonella , Shigella , and Yersinia , rely on type III secretion system (T3SS) effectors. We hypothesized that while hijacking processes within mammalian cells, the effectors operate as a robust network that can tolerate substantial contractions. This was tested in vivo using the mouse pathogen Citrobacter rodentium (encoding 31 effectors). Sequential gene deletions showed that effector essentiality for infection was context dependent and that the network could tolerate 60% contraction while maintaining pathogenicity. Despite inducing very different colonic cytokine profiles (e.g., interleukin-22, interleukin-17, interferon-γ, or granulocyte-macrophage colony-stimulating factor), different networks induced protective immunity. Using data from >100 distinct mutant combinations, we built and trained a machine learning model able to predict colonization outcomes, which were confirmed experimentally. Furthermore, reproducing the human-restricted enteropathogenic E. coli effector repertoire in C. rodentium was not sufficient for efficient colonization, which implicates effector networks in host adaptation. These results unveil the extreme robustness of both T3SS effector networks and host responses. [1]: /lookup/doi/10.1126/science.abc9531 [2]: pending:yes
领域	气候变化 ; 资源环境
URL	查看原文
引用统计	被引频次：46[WOS] [WOS记录] [WOS相关记录]
文献类型	期刊论文
条目标识符	http://119.78.100.173/C666/handle/2XK7JSWQ/318687
专题	气候变化资源环境科学
推荐引用方式 GB/T 7714	David Ruano-Gallego,Julia Sanchez-Garrido,Zuzanna Kozik,et al. Type III secretion system effectors form robust and flexible intracellular virulence networks[J]. Science,2021.
APA	David Ruano-Gallego.,Julia Sanchez-Garrido.,Zuzanna Kozik.,Elena Núñez-Berrueco.,Massiel Cepeda-Molero.,...&Gad Frankel.(2021).Type III secretion system effectors form robust and flexible intracellular virulence networks.Science.
MLA	David Ruano-Gallego,et al."Type III secretion system effectors form robust and flexible intracellular virulence networks".Science (2021).