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Heterologous complementation studies with the YscX and YscY protein families reveals a specificity for Yersinia pseudotuberculosis type III secretion
Umeå University, Faculty of Science and Technology, Department of Molecular Biology (Faculty of Science and Technology). Umeå University, Faculty of Medicine, Umeå Centre for Microbial Research (UCMR). (Francis)
Umeå University, Faculty of Science and Technology, Department of Molecular Biology (Faculty of Science and Technology). Umeå University, Faculty of Medicine, Umeå Centre for Microbial Research (UCMR). (Francis)
Umeå University, Faculty of Science and Technology, Department of Molecular Biology (Faculty of Science and Technology). Umeå University, Faculty of Medicine, Umeå Centre for Microbial Research (UCMR). (Francis)
Umeå University, Faculty of Science and Technology, Department of Molecular Biology (Faculty of Science and Technology). Umeå University, Faculty of Medicine, Umeå Centre for Microbial Research (UCMR). (Francis)
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2018 (English)In: Frontiers in Cellular and Infection Microbiology, E-ISSN 2235-2988, Vol. 8, article id 80Article in journal (Refereed) Published
Abstract [en]

Type III secretion systems harbored by several Gram-negative bacteria are often used to deliver host-modulating effectors into infected eukaryotic cells. About 20 core proteins are needed for assembly of a secretion apparatus. Several of these proteins are genetically and functionally conserved in type III secretion systems of bacteria associated with invertebrate or vertebrate hosts. In the Ysc family of type III secretion systems are two poorly characterized protein families, the YscX family and the YscY family. In the plasmid-encoded Ysc-Yop type III secretion system of human pathogenic Yersinia species, YscX is a secreted substrate while YscY is its non-secreted cognate chaperone. Critically, neither an yscX nor yscY null mutant of Yersinia is capable of type III secretion. In this study, we show that the genetic equivalents of these proteins produced as components of other type III secretion systems of Pseudomonas aeruginosa (PscX and PscY), Aeromonas species (AscX and AscY), Vibrio species (VscX and VscY), and Photorhabdus luminescens (SctX and SctY) all possess an ability to interact with its native cognate partner and also establish cross-reciprocal binding to non-cognate partners as judged by a yeast two-hybrid assay. Moreover, a yeast three-hybrid assay also revealed that these heterodimeric complexes could maintain an interaction with YscV family members, a core membrane component of all type III secretion systems. Despite maintaining these molecular interactions, only expression of the native yscX in the near full-length yscX deletion and native yscY in the near full-length yscY deletion were able to complement for their general substrate secretion defects. Hence, YscX and YscY must have co-evolved to confer an important function specifically critical for Yersinia type III secretion.

Place, publisher, year, edition, pages
Frontiers Research Foundation , 2018. Vol. 8, article id 80
Keywords [en]
T3S chaperone, secretion hierarchy, substrate sorting, LcrH/SycD, YscV, protein-protein interaction
National Category
Microbiology
Research subject
Microbiology; Molecular Biology; Infectious Diseases
Identifiers
URN: urn:nbn:se:umu:diva-146348DOI: 10.3389/fcimb.2018.00080ISI: 000427608900001PubMedID: 29616194Scopus ID: 2-s2.0-85044364781OAI: oai:DiVA.org:umu-146348DiVA, id: diva2:1195588
Funder
Swedish Research CouncilAvailable from: 2018-04-05 Created: 2018-04-05 Last updated: 2023-03-24Bibliographically approved
In thesis
1. Coordinating type III secretion system biogenesis in Yersinia pseudotuberculosis
Open this publication in new window or tab >>Coordinating type III secretion system biogenesis in Yersinia pseudotuberculosis
2020 (English)Doctoral thesis, comprehensive summary (Other academic)
Abstract [en]

Various Gram-negative bacteria utilize type III secretion system (T3SS) to deliver effectors into eukaryotic host cells and establish mutualistic or pathogenic interactions. An example is the Ysc-Yop T3SS of pathogenic Yersinia species. The T3SS resembles a molecular syringe with a wide cylindrical membrane-spanning basal body that scaffolds a hollow extracellular needle with a pore-forming translocon complex crowned at the needle tip. Together they form a continuous conduit between bacteria and host cells that allow delivery of effector proteins. 

Dedicated actions of cytoplasmic chaperones, regulators and components of the cytoplasmic complex orchestrates hierarchical assembly of T3SS. On the basis of secretion hierarchy, proteins can be categorized as ‘early’ needle complex proteins, ‘middle’ translocators and ‘late’ Yop effectors. However, how the system recognizes, prepares and mediates temporal delivery of T3S substrates is not fully understood. Herein, we have investigated the roles of YscX and YscY (present specifically in the Ysc family of T3SS), as well as YopN-TyeA (broadly distributed among T3SS families) to provide a better understanding of some of the molecular mechanisms governing spatiotemporal control of T3SS assembly.

Despite reciprocal YscX-YscY binary and YscX-YscY-SctV ternary interactions between the member proteins, functional interchangeability in Yersinia was not successful. This revealed YscX and YscY must perform functions unique to Yersinia T3SS. Defined domain swapping and site-directed mutagenesis identified two highly conserved cysteine residues important for YscX function. Moreover, the N-terminal region of YscX harboured an independent T3S signal. Manipulating the YscX N-terminus by exchanging it with equivalent secretion signals from different T3S substrates abrogated T3S activity. This was explained by the need for the YscX N-terminus to correctly localize and/or assemble the ‘early’ SctI inner adapter and SctF needle protein. Therefore, N-terminal YscX performs dual functions; one as a secretion signal and the other as a structural signal to control early stage assembly of T3SS.

In Ysc-Yop T3SS, YopN-TyeA complex is involved in the later stage of T3SS assembly, inhibiting Yops secretion until host cell contact is achieved. Analysis of the YopN C-terminus identified a specific domain stretching 279-287 critical for regulating Ysc-Yop T3SS activity. The regulation was mediated by specific hydrophobic contacts between W279 of YopN and F8 of TyeA.

In conclusion, this work has provided novel molecular mechanisms regarding  the spatiotemporal assembly of T3SS. While the N-terminal region of YscX contributes to the early stage of T3SS assembly, the C-terminal region of YopN is critical for regulating Ysc-Yop activity at a later stage of T3SS assembly.

Place, publisher, year, edition, pages
Umeå: Umeå University, 2020. p. 98
Keywords
Yersinia pseudotuberculosis, type III secretion system, YscX, YscY, YopN, TyeA, secretion signal, N-terminal region, site-directed mutagenesis
National Category
Microbiology Cell and Molecular Biology
Research subject
Molecular Biology; Microbiology
Identifiers
urn:nbn:se:umu:diva-174085 (URN)978-91-7855-338-9 (ISBN)978-91-7855-337-2 (ISBN)
Public defence
2020-09-11, Hörsal 933 Unod B 9, Norrlands universitetssjukhus, Umeå, 09:00 (English)
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Supervisors
Available from: 2020-08-21 Created: 2020-08-14 Last updated: 2024-07-02Bibliographically approved

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Gurung, Jyoti M.Amer, AyadFrancis, MonikaCosta, TiagoFrancis, Matthew S.

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