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Live-Attenuated Oral Vaccines to Reduce Campylobacter Colonization in Poultry

The control of Campylobacter in poultry at the pre-harvest level is critical to reducing foodborne infections with Campylobacter since the consumption of contaminated poultry is the most frequent cause of human campylobacteriosis. Although poultry vaccination is suggested as useful intervention meas...

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Autores principales: Jeon, Byeonghwa, Saisom, Tunchanok, Sasipreeyajan, Jiroj, Luangtongkum, Taradon
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9143049/
https://www.ncbi.nlm.nih.gov/pubmed/35632441
http://dx.doi.org/10.3390/vaccines10050685
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author Jeon, Byeonghwa
Saisom, Tunchanok
Sasipreeyajan, Jiroj
Luangtongkum, Taradon
author_facet Jeon, Byeonghwa
Saisom, Tunchanok
Sasipreeyajan, Jiroj
Luangtongkum, Taradon
author_sort Jeon, Byeonghwa
collection PubMed
description The control of Campylobacter in poultry at the pre-harvest level is critical to reducing foodborne infections with Campylobacter since the consumption of contaminated poultry is the most frequent cause of human campylobacteriosis. Although poultry vaccination is suggested as useful intervention measures, no Campylobacter vaccines are currently available. To develop live-attenuated oral Campylobacter vaccines, in this study, we evaluated the efficacy of pre-colonization by oxidative stress defense mutants, including knockout mutants of ahpC, katA, and sodB, in preventing Campylobacter jejuni from colonizing poultry. Interestingly, when chickens were pre-colonized with ΔahpC and ΔkatA mutants, rather than the ΔsodB mutant, the level of C. jejuni colonization was significantly reduced within 35 days. Further studies demonstrated when chickens were pre-colonized with the ΔahpC mutant by oral challenge with a high dose (ca., 5 × 10(8) CFU/bird) and a low dose (ca., 5 × 10(6) CFU/bird), it twice reduced the level of C. jejuni by 3.9 log(10)CFU/g feces and 3 log(10)CFU/g feces after 42 days, respectively, compared to the untreated control. Due to a colonization defect, the ΔahpC mutant was removed from chickens within 42 days. After excretion from the host, moreover, the ΔahpC mutant cannot survive in aerobic environments because of compromised aerotolerance. Our findings suggest that the ahpC mutant has a great potential for on-farm application to control C. jejuni at the pre-harvest level.
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spelling pubmed-91430492022-05-29 Live-Attenuated Oral Vaccines to Reduce Campylobacter Colonization in Poultry Jeon, Byeonghwa Saisom, Tunchanok Sasipreeyajan, Jiroj Luangtongkum, Taradon Vaccines (Basel) Article The control of Campylobacter in poultry at the pre-harvest level is critical to reducing foodborne infections with Campylobacter since the consumption of contaminated poultry is the most frequent cause of human campylobacteriosis. Although poultry vaccination is suggested as useful intervention measures, no Campylobacter vaccines are currently available. To develop live-attenuated oral Campylobacter vaccines, in this study, we evaluated the efficacy of pre-colonization by oxidative stress defense mutants, including knockout mutants of ahpC, katA, and sodB, in preventing Campylobacter jejuni from colonizing poultry. Interestingly, when chickens were pre-colonized with ΔahpC and ΔkatA mutants, rather than the ΔsodB mutant, the level of C. jejuni colonization was significantly reduced within 35 days. Further studies demonstrated when chickens were pre-colonized with the ΔahpC mutant by oral challenge with a high dose (ca., 5 × 10(8) CFU/bird) and a low dose (ca., 5 × 10(6) CFU/bird), it twice reduced the level of C. jejuni by 3.9 log(10)CFU/g feces and 3 log(10)CFU/g feces after 42 days, respectively, compared to the untreated control. Due to a colonization defect, the ΔahpC mutant was removed from chickens within 42 days. After excretion from the host, moreover, the ΔahpC mutant cannot survive in aerobic environments because of compromised aerotolerance. Our findings suggest that the ahpC mutant has a great potential for on-farm application to control C. jejuni at the pre-harvest level. MDPI 2022-04-27 /pmc/articles/PMC9143049/ /pubmed/35632441 http://dx.doi.org/10.3390/vaccines10050685 Text en © 2022 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Jeon, Byeonghwa
Saisom, Tunchanok
Sasipreeyajan, Jiroj
Luangtongkum, Taradon
Live-Attenuated Oral Vaccines to Reduce Campylobacter Colonization in Poultry
title Live-Attenuated Oral Vaccines to Reduce Campylobacter Colonization in Poultry
title_full Live-Attenuated Oral Vaccines to Reduce Campylobacter Colonization in Poultry
title_fullStr Live-Attenuated Oral Vaccines to Reduce Campylobacter Colonization in Poultry
title_full_unstemmed Live-Attenuated Oral Vaccines to Reduce Campylobacter Colonization in Poultry
title_short Live-Attenuated Oral Vaccines to Reduce Campylobacter Colonization in Poultry
title_sort live-attenuated oral vaccines to reduce campylobacter colonization in poultry
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9143049/
https://www.ncbi.nlm.nih.gov/pubmed/35632441
http://dx.doi.org/10.3390/vaccines10050685
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