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Characterization of Temperate LPS-Binding Bordetella avium Phages That Lack Superinfection Immunity

Bordetella avium causes a highly infectious upper respiratory tract disease in turkeys and other poultry with high economic losses. Considering the antimicrobial resistance crisis, bacteriophages (phages) may be an alternative approach for treating bacterial infections such as bordetellosis. Here, w...

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Autores principales: Serian, Dorothee, Churin, Yury, Hammerl, Jens André, Rohde, Manfred, Jung, Arne, Müller, Anja, Yue, Min, Kehrenberg, Corinna
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Society for Microbiology 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10269795/
https://www.ncbi.nlm.nih.gov/pubmed/37125905
http://dx.doi.org/10.1128/spectrum.03702-22
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author Serian, Dorothee
Churin, Yury
Hammerl, Jens André
Rohde, Manfred
Jung, Arne
Müller, Anja
Yue, Min
Kehrenberg, Corinna
author_facet Serian, Dorothee
Churin, Yury
Hammerl, Jens André
Rohde, Manfred
Jung, Arne
Müller, Anja
Yue, Min
Kehrenberg, Corinna
author_sort Serian, Dorothee
collection PubMed
description Bordetella avium causes a highly infectious upper respiratory tract disease in turkeys and other poultry with high economic losses. Considering the antimicrobial resistance crisis, bacteriophages (phages) may be an alternative approach for treating bacterial infections such as bordetellosis. Here, we describe seven B. avium phages, isolated from drinking water and feces from chicken and turkey farms. They showed strong bacteriolytic activity with a broad host range and used lipopolysaccharides (LPS) as a host receptor for their adsorption. All phages are myoviruses based on their structure observed by transmission electron microscopy. Genome sequence analyses revealed genome assembly sizes ranging from 39,087 to 43,144 bp. Their permutated genomes were organized colinearly, with a conserved module order, and were packed according to a predicted headful packing strategy. Notably, they contained genes encoding putative markers of lysogeny, indicative of temperate phages, despite their lytic phenotype. Further investigation revealed that the phages could indeed undergo a lysogenic life cycle with varying frequency. However, the lysogenic bacteria were still susceptible to superinfection with the same phages. This lack of stable superinfection immunity after lysogenization appears to be a characteristic feature of B. avium phages, which is favorable in terms of a potential therapeutic use of phages for the treatment of avian bordetellosis. IMPORTANCE To maintain the effectiveness of antibiotics over the long term, alternatives to treat infectious diseases are urgently needed. Therefore, phages have recently come back into focus as they can specifically infect and lyse bacteria and are naturally occurring. However, there is little information on phages that can infect pathogenic bacteria from animals, such as the causative agent of bordetellosis of poultry, B. avium. Therefore, in this study, B. avium phages were isolated and comprehensively characterized, including whole-genome analysis. Although phenotypically the phages were thought to undergo a lytic cycle, we demonstrated that they undergo a lysogenic phase, but that infection does not confer stable host superinfection immunity. These findings provide important information that could be relevant for potential biocontrol of avian bordetellosis by using phage therapy.
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spelling pubmed-102697952023-06-16 Characterization of Temperate LPS-Binding Bordetella avium Phages That Lack Superinfection Immunity Serian, Dorothee Churin, Yury Hammerl, Jens André Rohde, Manfred Jung, Arne Müller, Anja Yue, Min Kehrenberg, Corinna Microbiol Spectr Research Article Bordetella avium causes a highly infectious upper respiratory tract disease in turkeys and other poultry with high economic losses. Considering the antimicrobial resistance crisis, bacteriophages (phages) may be an alternative approach for treating bacterial infections such as bordetellosis. Here, we describe seven B. avium phages, isolated from drinking water and feces from chicken and turkey farms. They showed strong bacteriolytic activity with a broad host range and used lipopolysaccharides (LPS) as a host receptor for their adsorption. All phages are myoviruses based on their structure observed by transmission electron microscopy. Genome sequence analyses revealed genome assembly sizes ranging from 39,087 to 43,144 bp. Their permutated genomes were organized colinearly, with a conserved module order, and were packed according to a predicted headful packing strategy. Notably, they contained genes encoding putative markers of lysogeny, indicative of temperate phages, despite their lytic phenotype. Further investigation revealed that the phages could indeed undergo a lysogenic life cycle with varying frequency. However, the lysogenic bacteria were still susceptible to superinfection with the same phages. This lack of stable superinfection immunity after lysogenization appears to be a characteristic feature of B. avium phages, which is favorable in terms of a potential therapeutic use of phages for the treatment of avian bordetellosis. IMPORTANCE To maintain the effectiveness of antibiotics over the long term, alternatives to treat infectious diseases are urgently needed. Therefore, phages have recently come back into focus as they can specifically infect and lyse bacteria and are naturally occurring. However, there is little information on phages that can infect pathogenic bacteria from animals, such as the causative agent of bordetellosis of poultry, B. avium. Therefore, in this study, B. avium phages were isolated and comprehensively characterized, including whole-genome analysis. Although phenotypically the phages were thought to undergo a lytic cycle, we demonstrated that they undergo a lysogenic phase, but that infection does not confer stable host superinfection immunity. These findings provide important information that could be relevant for potential biocontrol of avian bordetellosis by using phage therapy. American Society for Microbiology 2023-05-01 /pmc/articles/PMC10269795/ /pubmed/37125905 http://dx.doi.org/10.1128/spectrum.03702-22 Text en Copyright © 2023 Serian et al. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution 4.0 International license (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Research Article
Serian, Dorothee
Churin, Yury
Hammerl, Jens André
Rohde, Manfred
Jung, Arne
Müller, Anja
Yue, Min
Kehrenberg, Corinna
Characterization of Temperate LPS-Binding Bordetella avium Phages That Lack Superinfection Immunity
title Characterization of Temperate LPS-Binding Bordetella avium Phages That Lack Superinfection Immunity
title_full Characterization of Temperate LPS-Binding Bordetella avium Phages That Lack Superinfection Immunity
title_fullStr Characterization of Temperate LPS-Binding Bordetella avium Phages That Lack Superinfection Immunity
title_full_unstemmed Characterization of Temperate LPS-Binding Bordetella avium Phages That Lack Superinfection Immunity
title_short Characterization of Temperate LPS-Binding Bordetella avium Phages That Lack Superinfection Immunity
title_sort characterization of temperate lps-binding bordetella avium phages that lack superinfection immunity
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10269795/
https://www.ncbi.nlm.nih.gov/pubmed/37125905
http://dx.doi.org/10.1128/spectrum.03702-22
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