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Reprogramming of Yersinia from Virulent to Persistent Mode Revealed by Complex In Vivo RNA-seq Analysis
Umeå universitet, Medicinska fakulteten, Umeå Centre for Microbial Research (UCMR). Umeå universitet, Medicinska fakulteten, Molekylär Infektionsmedicin, Sverige (MIMS). Umeå universitet, Medicinska fakulteten, Institutionen för molekylärbiologi (Medicinska fakulteten). (Maria Fällman)
Umeå universitet, Medicinska fakulteten, Institutionen för molekylärbiologi (Medicinska fakulteten). Umeå universitet, Medicinska fakulteten, Umeå Centre for Microbial Research (UCMR).
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2015 (Engelska)Ingår i: PLoS Pathogens, ISSN 1553-7366, E-ISSN 1553-7374, Vol. 11, nr 1, artikel-id e1004600Artikel i tidskrift (Refereegranskat) Published
Abstract [en]

We recently found that Yersinia pseudotuberculosis can be used as a model of persistent bacterial infections. We performed in vivo RNA-seq of bacteria in small cecal tissue biopsies at early and persistent stages of infection to determine strategies associated with persistence. Comprehensive analysis of mixed RNA populations from infected tissues revealed that Y. pseudotuberculosis undergoes transcriptional reprogramming with drastic down-regulation of T3SS virulence genes during persistence when the pathogen resides within the cecum. At the persistent stage, the expression pattern in many respects resembles the pattern seen in vitro at 26oC, with for example, up-regulation of flagellar genes and invA. These findings are expected to have impact on future rationales to identify suitable bacterial targets for new antibiotics. Other genes that are up-regulated during persistence are genes involved in anaerobiosis, chemotaxis, and protection against oxidative and acidic stress, which indicates the influence of different environmental cues. We found that the Crp/CsrA/RovA regulatory cascades influence the pattern of bacterial gene expression during persistence. Furthermore, arcA, fnr, frdA, and wrbA play critical roles in persistence. Our findings suggest a model for the life cycle of this enteropathogen with reprogramming from a virulent to an adapted phenotype capable of persisting and spreading by fecal shedding.

Ort, förlag, år, upplaga, sidor
2015. Vol. 11, nr 1, artikel-id e1004600
Nyckelord [en]
Persistent infection, RNA-seq, PMNs, Yersinia, Transcriptome, wrba, fnr, rovA, arcA, rfaH
Nationell ämneskategori
Cell- och molekylärbiologi Biokemi och molekylärbiologi Bioinformatik och systembiologi
Forskningsämne
biologi, miljövetenskap
Identifikatorer
URN: urn:nbn:se:umu:diva-100980DOI: 10.1371/journal.ppat.1004600ISI: 000349106100030PubMedID: 25590628OAI: oai:DiVA.org:umu-100980DiVA, id: diva2:795468
Tillgänglig från: 2015-03-16 Skapad: 2015-03-16 Senast uppdaterad: 2018-06-07Bibliografiskt granskad
Ingår i avhandling
1. Persistent infection by Yersinia pseudotuberculosis
Öppna denna publikation i ny flik eller fönster >>Persistent infection by Yersinia pseudotuberculosis
2015 (Engelska)Doktorsavhandling, sammanläggning (Övrigt vetenskapligt)
Abstract [en]

Enteropathogenic Yersinia species can infect many mammalian organs such as the small intestine, cecum, Peyer’s patches, liver, spleen, and lung and cause diseases that resemble a typhoid-like syndrome, as seen for other enteropathogens. We found that sublethal infection doses of Y. pseudotuberculosis gave rise to asymptomatic persistent infection in mice and identified the cecal lymphoid follicles as the primary site for colonization during persistence. Persistent Y. pseudotuberculosis is localized in the dome area, often in inflammatory lesions, as foci or as single cells, and also in neutrophil exudates in the cecal lumen. This new mouse model for bacterial persistence in cecum has potential as an investigative tool for deeper understanding of bacterial adaptation and host immune defense mechanisms during persistent infection. Here, we investigated the nature of the persistent infection established by Y. pseudotuberculosis in mouse cecal tissue using in vivo RNA-seq of bacteria during early and persistent stages of infection. Comparative analysis of the bacterial transcriptomes revealed that Y. pseudotuberculosis undergoes transcriptional reprogramming with drastic down-regulation of T3SS virulence genes during persistence in the cecum. At the persistent stage, the expression pattern in many respects resembles the pattern seen in vitro at 26°C. Genes that are up-regulated during persistence are genes involved in anaerobiosis, chemotaxis, and protection against oxidative and acidic stress, which indicates the influence of different environmental cues. We found that the Crp/CsrA/RovA regulatory cascades influence the pattern of bacterial gene expression during persistence. Furthermore, we show that ArcA, Fnr, FrdA, WrbA, RovA, and RfaH play critical roles in persistence. An extended investigation of the transcriptional regulator rfaH employing mouse infection studies, phenotypic characterizations, and RNA-seq transcriptomics analyses indicated that this gene product contributes to establishment of infection and confirmed that it regulates O-antigen biosynthesis genes in Y. pseudotuberculosis. The RNA-seq results also suggest that rfaH has a relatively global effect. Furthermore, we also found that the dynamics of the cecal tissue organization and microbial composition shows changes during different stages of the infection. Taken together, based on our findings, we speculate that this enteropathogen initiates infection by using its virulence factors in meeting the innate immune response in the cecal tissue. Later on, these factors lead to dysbiosis in the local microbiota and altered tissue organization. At later stages of the infection, the pathogen adapts to the environment in the cecum by reprogramming its transcriptome from a highly virulent mode to a more environmentally adaptable mode for survival and shedding. The in vivo transcriptomic analyses for essential genes during infections present strong candidates for novel targets for antimicrobials.

Ort, förlag, år, upplaga, sidor
Umeå: Umeå University, 2015. s. 72
Serie
Umeå University medical dissertations, ISSN 0346-6612 ; 1748
Nyckelord
Persistent infection, RNA-seq, PMNs, Yersinia, Transcriptome, wrba, fnr, rovA, arcA, rfaH
Nationell ämneskategori
Mikrobiologi Bioinformatik och systembiologi Biokemi och molekylärbiologi
Forskningsämne
molekylärbiologi; infektionssjukdomar; immunologi
Identifikatorer
urn:nbn:se:umu:diva-108837 (URN)978-91-7601-335-9 (ISBN)
Disputation
2015-10-09, Sal E04, byggnad 6E, NUS, Umeå, 09:00 (Engelska)
Opponent
Handledare
Tillgänglig från: 2015-09-18 Skapad: 2015-09-15 Senast uppdaterad: 2018-06-07Bibliografiskt granskad

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Avican, KemalFahlgren, AnnaFällman, Maria

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Umeå Centre for Microbial Research (UCMR)Molekylär Infektionsmedicin, Sverige (MIMS)Institutionen för molekylärbiologi (Medicinska fakulteten)
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