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Rickettsia conorii Transcriptional Response within Inoculation Eschar

BACKGROUND: Rickettsia conorii, the causative agent of the Mediterranean spotted fever, is transmitted to humans by the bite of infected ticks Rhipicephalus sanguineus. The skin thus constitutes an important barrier for the entry and propagation of R. conorii. Given this, analysis of the survival st...

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Autores principales: Renesto, Patricia, Rovery, Clarisse, Schrenzel, Jacques, Leroy, Quentin, Huyghe, Antoine, Li, Wenjun, Lepidi, Hubert, François, Patrice, Raoult, Didier
Formato: Texto
Lenguaje:English
Publicado: Public Library of Science 2008
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2577010/
https://www.ncbi.nlm.nih.gov/pubmed/18997861
http://dx.doi.org/10.1371/journal.pone.0003681
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author Renesto, Patricia
Rovery, Clarisse
Schrenzel, Jacques
Leroy, Quentin
Huyghe, Antoine
Li, Wenjun
Lepidi, Hubert
François, Patrice
Raoult, Didier
author_facet Renesto, Patricia
Rovery, Clarisse
Schrenzel, Jacques
Leroy, Quentin
Huyghe, Antoine
Li, Wenjun
Lepidi, Hubert
François, Patrice
Raoult, Didier
author_sort Renesto, Patricia
collection PubMed
description BACKGROUND: Rickettsia conorii, the causative agent of the Mediterranean spotted fever, is transmitted to humans by the bite of infected ticks Rhipicephalus sanguineus. The skin thus constitutes an important barrier for the entry and propagation of R. conorii. Given this, analysis of the survival strategies used by the bacterium within infected skin is critical for our understanding of rickettsiosis. METHODOLOGY/PRINCIPAL FINDINGS: Here, we report the first genome-wide analysis of R. conorii gene expression from infected human skin biopsies. Our data showed that R. conorii exhibited a striking transcript signature that is remarkably conserved across patients, regardless of genotype. The expression profiles obtained using custom Agilent microarrays were validated by quantitative RT-PCR. Within eschars, the amount of detected R. conorii transcripts was of 55%, this value being of 74% for bacteria grown in Vero cells. In such infected host tissues, approximately 15% (n = 211) of the total predicted R. conorii ORFs appeared differentially expressed compared to bacteria grown in standard laboratory conditions. These genes are mostly down-regulated and encode proteins essential for bacterial replication. Some of the strategies displayed by rickettsiae to overcome the host defense barriers, thus avoiding killing, were also pointed out. The observed up-regulation of rickettsial genes associated with DNA repair is likely to correspond to a DNA-damaging agent enriched environment generated by the host cells to eradicate the pathogens. Survival of R. conorii within eschars also involves adaptation to osmotic stress, changes in cell surface proteins and up-regulation of some virulence factors. Interestingly, in contrast to down-regulated transcripts, we noticed that up-regulated ones rather exhibit a small nucleotide size, most of them being exclusive for the spotted fever group rickettsiae. CONCLUSION/SIGNIFICANCE: Because eschar is a site for rickettsial introduction, the pattern of rickettsial gene expression observed here may define how rickettsiae counteract the host defense.
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spelling pubmed-25770102008-11-10 Rickettsia conorii Transcriptional Response within Inoculation Eschar Renesto, Patricia Rovery, Clarisse Schrenzel, Jacques Leroy, Quentin Huyghe, Antoine Li, Wenjun Lepidi, Hubert François, Patrice Raoult, Didier PLoS One Research Article BACKGROUND: Rickettsia conorii, the causative agent of the Mediterranean spotted fever, is transmitted to humans by the bite of infected ticks Rhipicephalus sanguineus. The skin thus constitutes an important barrier for the entry and propagation of R. conorii. Given this, analysis of the survival strategies used by the bacterium within infected skin is critical for our understanding of rickettsiosis. METHODOLOGY/PRINCIPAL FINDINGS: Here, we report the first genome-wide analysis of R. conorii gene expression from infected human skin biopsies. Our data showed that R. conorii exhibited a striking transcript signature that is remarkably conserved across patients, regardless of genotype. The expression profiles obtained using custom Agilent microarrays were validated by quantitative RT-PCR. Within eschars, the amount of detected R. conorii transcripts was of 55%, this value being of 74% for bacteria grown in Vero cells. In such infected host tissues, approximately 15% (n = 211) of the total predicted R. conorii ORFs appeared differentially expressed compared to bacteria grown in standard laboratory conditions. These genes are mostly down-regulated and encode proteins essential for bacterial replication. Some of the strategies displayed by rickettsiae to overcome the host defense barriers, thus avoiding killing, were also pointed out. The observed up-regulation of rickettsial genes associated with DNA repair is likely to correspond to a DNA-damaging agent enriched environment generated by the host cells to eradicate the pathogens. Survival of R. conorii within eschars also involves adaptation to osmotic stress, changes in cell surface proteins and up-regulation of some virulence factors. Interestingly, in contrast to down-regulated transcripts, we noticed that up-regulated ones rather exhibit a small nucleotide size, most of them being exclusive for the spotted fever group rickettsiae. CONCLUSION/SIGNIFICANCE: Because eschar is a site for rickettsial introduction, the pattern of rickettsial gene expression observed here may define how rickettsiae counteract the host defense. Public Library of Science 2008-11-10 /pmc/articles/PMC2577010/ /pubmed/18997861 http://dx.doi.org/10.1371/journal.pone.0003681 Text en Renesto et al. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Renesto, Patricia
Rovery, Clarisse
Schrenzel, Jacques
Leroy, Quentin
Huyghe, Antoine
Li, Wenjun
Lepidi, Hubert
François, Patrice
Raoult, Didier
Rickettsia conorii Transcriptional Response within Inoculation Eschar
title Rickettsia conorii Transcriptional Response within Inoculation Eschar
title_full Rickettsia conorii Transcriptional Response within Inoculation Eschar
title_fullStr Rickettsia conorii Transcriptional Response within Inoculation Eschar
title_full_unstemmed Rickettsia conorii Transcriptional Response within Inoculation Eschar
title_short Rickettsia conorii Transcriptional Response within Inoculation Eschar
title_sort rickettsia conorii transcriptional response within inoculation eschar
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2577010/
https://www.ncbi.nlm.nih.gov/pubmed/18997861
http://dx.doi.org/10.1371/journal.pone.0003681
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