Cargando…

High-Frequency Variation of Purine Biosynthesis Genes Is a Mechanism of Success in Campylobacter jejuni

Phenotypic variation is prevalent in the zoonotic pathogen Campylobacter jejuni, the leading agent of enterocolitis in the developed world. Heterogeneity enhances the survival and adaptive malleability of bacterial populations because variable phenotypes may allow some cells to be protected against...

Descripción completa

Detalles Bibliográficos
Autores principales: Cameron, Andrew, Huynh, Steven, Scott, Nichollas E., Frirdich, Emilisa, Apel, Dmitry, Foster, Leonard J., Parker, Craig T., Gaynor, Erin C.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Society of Microbiology 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4611032/
https://www.ncbi.nlm.nih.gov/pubmed/26419875
http://dx.doi.org/10.1128/mBio.00612-15
_version_ 1782396037071110144
author Cameron, Andrew
Huynh, Steven
Scott, Nichollas E.
Frirdich, Emilisa
Apel, Dmitry
Foster, Leonard J.
Parker, Craig T.
Gaynor, Erin C.
author_facet Cameron, Andrew
Huynh, Steven
Scott, Nichollas E.
Frirdich, Emilisa
Apel, Dmitry
Foster, Leonard J.
Parker, Craig T.
Gaynor, Erin C.
author_sort Cameron, Andrew
collection PubMed
description Phenotypic variation is prevalent in the zoonotic pathogen Campylobacter jejuni, the leading agent of enterocolitis in the developed world. Heterogeneity enhances the survival and adaptive malleability of bacterial populations because variable phenotypes may allow some cells to be protected against future stress. Exposure to hyperosmotic stress previously revealed prevalent differences in growth between C. jejuni strain 81-176 colonies due to resistant or sensitive phenotypes, and these isolated colonies continued to produce progeny with differential phenotypes. In this study, whole-genome sequencing of isolated colonies identified allelic variants of two purine biosynthesis genes, purF and apt, encoding phosphoribosyltransferases that utilize a shared substrate. Genetic analyses determined that purF was essential for fitness, while apt was critical. Traditional and high-depth amplicon-sequencing analyses confirmed extensive intrapopulation genetic variation of purF and apt that resulted in viable strains bearing alleles with in-frame insertion duplications, deletions, or missense polymorphisms. Different purF and apt alleles were associated with various stress survival capabilities under several niche-relevant conditions and contributed to differential intracellular survival in an epithelial cell infection model. Amplicon sequencing revealed that intracellular survival selected for stress-fit purF and apt alleles, as did exposure to oxygen and hyperosmotic stress. Putative protein recognition direct repeat sequences were identified in purF and apt, and a DNA-protein affinity screen captured a predicted exonuclease that promoted the global spontaneous mutation rate. This work illustrates the adaptive properties of high-frequency genetic variation in two housekeeping genes, which influences C. jejuni survival under stress and promotes its success as a pathogen.
format Online
Article
Text
id pubmed-4611032
institution National Center for Biotechnology Information
language English
publishDate 2015
publisher American Society of Microbiology
record_format MEDLINE/PubMed
spelling pubmed-46110322015-10-25 High-Frequency Variation of Purine Biosynthesis Genes Is a Mechanism of Success in Campylobacter jejuni Cameron, Andrew Huynh, Steven Scott, Nichollas E. Frirdich, Emilisa Apel, Dmitry Foster, Leonard J. Parker, Craig T. Gaynor, Erin C. mBio Research Article Phenotypic variation is prevalent in the zoonotic pathogen Campylobacter jejuni, the leading agent of enterocolitis in the developed world. Heterogeneity enhances the survival and adaptive malleability of bacterial populations because variable phenotypes may allow some cells to be protected against future stress. Exposure to hyperosmotic stress previously revealed prevalent differences in growth between C. jejuni strain 81-176 colonies due to resistant or sensitive phenotypes, and these isolated colonies continued to produce progeny with differential phenotypes. In this study, whole-genome sequencing of isolated colonies identified allelic variants of two purine biosynthesis genes, purF and apt, encoding phosphoribosyltransferases that utilize a shared substrate. Genetic analyses determined that purF was essential for fitness, while apt was critical. Traditional and high-depth amplicon-sequencing analyses confirmed extensive intrapopulation genetic variation of purF and apt that resulted in viable strains bearing alleles with in-frame insertion duplications, deletions, or missense polymorphisms. Different purF and apt alleles were associated with various stress survival capabilities under several niche-relevant conditions and contributed to differential intracellular survival in an epithelial cell infection model. Amplicon sequencing revealed that intracellular survival selected for stress-fit purF and apt alleles, as did exposure to oxygen and hyperosmotic stress. Putative protein recognition direct repeat sequences were identified in purF and apt, and a DNA-protein affinity screen captured a predicted exonuclease that promoted the global spontaneous mutation rate. This work illustrates the adaptive properties of high-frequency genetic variation in two housekeeping genes, which influences C. jejuni survival under stress and promotes its success as a pathogen. American Society of Microbiology 2015-09-29 /pmc/articles/PMC4611032/ /pubmed/26419875 http://dx.doi.org/10.1128/mBio.00612-15 Text en Copyright © 2015 Cameron et al. http://creativecommons.org/licenses/by-nc-sa/3.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution-Noncommercial-ShareAlike 3.0 Unported license (http://creativecommons.org/licenses/by-nc-sa/3.0/) , which permits unrestricted noncommercial use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Article
Cameron, Andrew
Huynh, Steven
Scott, Nichollas E.
Frirdich, Emilisa
Apel, Dmitry
Foster, Leonard J.
Parker, Craig T.
Gaynor, Erin C.
High-Frequency Variation of Purine Biosynthesis Genes Is a Mechanism of Success in Campylobacter jejuni
title High-Frequency Variation of Purine Biosynthesis Genes Is a Mechanism of Success in Campylobacter jejuni
title_full High-Frequency Variation of Purine Biosynthesis Genes Is a Mechanism of Success in Campylobacter jejuni
title_fullStr High-Frequency Variation of Purine Biosynthesis Genes Is a Mechanism of Success in Campylobacter jejuni
title_full_unstemmed High-Frequency Variation of Purine Biosynthesis Genes Is a Mechanism of Success in Campylobacter jejuni
title_short High-Frequency Variation of Purine Biosynthesis Genes Is a Mechanism of Success in Campylobacter jejuni
title_sort high-frequency variation of purine biosynthesis genes is a mechanism of success in campylobacter jejuni
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4611032/
https://www.ncbi.nlm.nih.gov/pubmed/26419875
http://dx.doi.org/10.1128/mBio.00612-15
work_keys_str_mv AT cameronandrew highfrequencyvariationofpurinebiosynthesisgenesisamechanismofsuccessincampylobacterjejuni
AT huynhsteven highfrequencyvariationofpurinebiosynthesisgenesisamechanismofsuccessincampylobacterjejuni
AT scottnichollase highfrequencyvariationofpurinebiosynthesisgenesisamechanismofsuccessincampylobacterjejuni
AT frirdichemilisa highfrequencyvariationofpurinebiosynthesisgenesisamechanismofsuccessincampylobacterjejuni
AT apeldmitry highfrequencyvariationofpurinebiosynthesisgenesisamechanismofsuccessincampylobacterjejuni
AT fosterleonardj highfrequencyvariationofpurinebiosynthesisgenesisamechanismofsuccessincampylobacterjejuni
AT parkercraigt highfrequencyvariationofpurinebiosynthesisgenesisamechanismofsuccessincampylobacterjejuni
AT gaynorerinc highfrequencyvariationofpurinebiosynthesisgenesisamechanismofsuccessincampylobacterjejuni