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Identification of Novel Phage Resistance Mechanisms in Campylobacter jejuni by Comparative Genomics

Phages infecting Campylobacter jejuni are considered a promising intervention strategy at broiler farms, yet phage sensitivity of naturally occurring poultry isolates is not well studied. Here, we investigated phage sensitivity and identified resistance mechanisms of C. jejuni strains originating fr...

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Autores principales: Sørensen, Martine C. H., Gencay, Yilmaz Emre, Fanger, Florian, Chichkova, Mariana A. T., Mazúrová, Mária, Klumpp, Jochen, Nielsen, Eva M., Brøndsted, Lone
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8713573/
https://www.ncbi.nlm.nih.gov/pubmed/34970240
http://dx.doi.org/10.3389/fmicb.2021.780559
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author Sørensen, Martine C. H.
Gencay, Yilmaz Emre
Fanger, Florian
Chichkova, Mariana A. T.
Mazúrová, Mária
Klumpp, Jochen
Nielsen, Eva M.
Brøndsted, Lone
author_facet Sørensen, Martine C. H.
Gencay, Yilmaz Emre
Fanger, Florian
Chichkova, Mariana A. T.
Mazúrová, Mária
Klumpp, Jochen
Nielsen, Eva M.
Brøndsted, Lone
author_sort Sørensen, Martine C. H.
collection PubMed
description Phages infecting Campylobacter jejuni are considered a promising intervention strategy at broiler farms, yet phage sensitivity of naturally occurring poultry isolates is not well studied. Here, we investigated phage sensitivity and identified resistance mechanisms of C. jejuni strains originating from Danish broilers belonging to the most prevalent MLST (ST) types. Determining plaque formation of 51 phages belonging to Fletchervirus or Firehammervirus showed that 21 out of 31 C. jejuni strains were susceptible to at least one phage. While C. jejuni ST-21 strains encoded the common phase variable O-methyl phosphoramidate (MeOPN) receptor of the Fletchervirus and were only infected by these phages, ST-45 strains did not encode this receptor and were exclusively infected by Firehammervirus phages. To identify internal phage resistance mechanism in ST-21 strains, we performed comparative genomics of two strains, CAMSA2002 sensitive to almost all Fletchervirus phages and CAMSA2038, resistant to all 51 phages. The strains encoded diverse clustered regularly interspaced short palindromic repeats (CRISPR) spacers but none matched the tested phages. Sequence divergence was also observed in a predicted SspE homolog and putative restriction modification systems including a methyl-specific McrBC endonuclease. Furthermore, when mcrB was deleted, CAMSA2038 became sensitive to 17 out of 43 phages, three being Firehammervirus phages that otherwise did not infect any ST-21 strains. Yet, 16 phages demonstrated significantly lower efficiencies of plating on the mcrB mutant suggesting additional resistance mechanism still restricting phage propagation in CAMSA2038. Thus, our work demonstrates that C. jejuni isolates originating from broilers may have acquired several resistance mechanisms to successfully prevent phage infection in their natural habitat.
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spelling pubmed-87135732021-12-29 Identification of Novel Phage Resistance Mechanisms in Campylobacter jejuni by Comparative Genomics Sørensen, Martine C. H. Gencay, Yilmaz Emre Fanger, Florian Chichkova, Mariana A. T. Mazúrová, Mária Klumpp, Jochen Nielsen, Eva M. Brøndsted, Lone Front Microbiol Microbiology Phages infecting Campylobacter jejuni are considered a promising intervention strategy at broiler farms, yet phage sensitivity of naturally occurring poultry isolates is not well studied. Here, we investigated phage sensitivity and identified resistance mechanisms of C. jejuni strains originating from Danish broilers belonging to the most prevalent MLST (ST) types. Determining plaque formation of 51 phages belonging to Fletchervirus or Firehammervirus showed that 21 out of 31 C. jejuni strains were susceptible to at least one phage. While C. jejuni ST-21 strains encoded the common phase variable O-methyl phosphoramidate (MeOPN) receptor of the Fletchervirus and were only infected by these phages, ST-45 strains did not encode this receptor and were exclusively infected by Firehammervirus phages. To identify internal phage resistance mechanism in ST-21 strains, we performed comparative genomics of two strains, CAMSA2002 sensitive to almost all Fletchervirus phages and CAMSA2038, resistant to all 51 phages. The strains encoded diverse clustered regularly interspaced short palindromic repeats (CRISPR) spacers but none matched the tested phages. Sequence divergence was also observed in a predicted SspE homolog and putative restriction modification systems including a methyl-specific McrBC endonuclease. Furthermore, when mcrB was deleted, CAMSA2038 became sensitive to 17 out of 43 phages, three being Firehammervirus phages that otherwise did not infect any ST-21 strains. Yet, 16 phages demonstrated significantly lower efficiencies of plating on the mcrB mutant suggesting additional resistance mechanism still restricting phage propagation in CAMSA2038. Thus, our work demonstrates that C. jejuni isolates originating from broilers may have acquired several resistance mechanisms to successfully prevent phage infection in their natural habitat. Frontiers Media S.A. 2021-12-14 /pmc/articles/PMC8713573/ /pubmed/34970240 http://dx.doi.org/10.3389/fmicb.2021.780559 Text en Copyright © 2021 Sørensen, Gencay, Fanger, Chichkova, Mazúrová, Klumpp, Nielsen and Brøndsted. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Microbiology
Sørensen, Martine C. H.
Gencay, Yilmaz Emre
Fanger, Florian
Chichkova, Mariana A. T.
Mazúrová, Mária
Klumpp, Jochen
Nielsen, Eva M.
Brøndsted, Lone
Identification of Novel Phage Resistance Mechanisms in Campylobacter jejuni by Comparative Genomics
title Identification of Novel Phage Resistance Mechanisms in Campylobacter jejuni by Comparative Genomics
title_full Identification of Novel Phage Resistance Mechanisms in Campylobacter jejuni by Comparative Genomics
title_fullStr Identification of Novel Phage Resistance Mechanisms in Campylobacter jejuni by Comparative Genomics
title_full_unstemmed Identification of Novel Phage Resistance Mechanisms in Campylobacter jejuni by Comparative Genomics
title_short Identification of Novel Phage Resistance Mechanisms in Campylobacter jejuni by Comparative Genomics
title_sort identification of novel phage resistance mechanisms in campylobacter jejuni by comparative genomics
topic Microbiology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8713573/
https://www.ncbi.nlm.nih.gov/pubmed/34970240
http://dx.doi.org/10.3389/fmicb.2021.780559
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