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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...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2022
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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. |
format | Online Article Text |
id | pubmed-9143049 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
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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