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Role of aspartate ammonia-lyase in Pasteurella multocida

BACKGROUND: Pasteurella multocida is responsible for a highly infectious and contagious disease in birds, leading to heavy economic losses in the chicken industry. However, the pathogenesis of this disease is poorly understood. We recently identified an aspartate ammonia-lyase (aspA) in P. multocida...

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Autores principales: Wang, Zui, Li, Li, Liu, Peng, Wang, Chen, Lu, Qin, Liu, Lina, Wang, Xiaozhong, Luo, Qingping, Shao, Huabin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7713322/
https://www.ncbi.nlm.nih.gov/pubmed/33272193
http://dx.doi.org/10.1186/s12866-020-02049-2
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author Wang, Zui
Li, Li
Liu, Peng
Wang, Chen
Lu, Qin
Liu, Lina
Wang, Xiaozhong
Luo, Qingping
Shao, Huabin
author_facet Wang, Zui
Li, Li
Liu, Peng
Wang, Chen
Lu, Qin
Liu, Lina
Wang, Xiaozhong
Luo, Qingping
Shao, Huabin
author_sort Wang, Zui
collection PubMed
description BACKGROUND: Pasteurella multocida is responsible for a highly infectious and contagious disease in birds, leading to heavy economic losses in the chicken industry. However, the pathogenesis of this disease is poorly understood. We recently identified an aspartate ammonia-lyase (aspA) in P. multocida that was significantly upregulated under iron-restricted conditions, the protein of which could effectively protect chicken flocks against P. multocida. However, the functions of this gene remain unclear. In the present study, we constructed aspA mutant strain △aspA::kan and complementary strain C△aspA::kan to investigate the function of aspA in detail. RESULT: Deletion of the aspA gene in P. multocida resulted in a significant reduction in bacterial growth in LB (Luria-Bertani) and MH (Mueller-Hinton) media, which was rescued by supplementation with 20 mM fumarate. The mutant strain △aspA::kan showed significantly growth defects in anaerobic conditions and acid medium, compared with the wild-type strain. Moreover, growth of △aspA::kan was more seriously impaired than that of the wild-type strain under iron-restricted conditions, and this growth recovered after supplementation with iron ions. AspA transcription was negatively regulated by iron conditions, as demonstrated by quantitative reverse transcription-polymerase chain reaction. Although competitive index assay showed the wild-type strain outcompetes the aspA mutant strain and △aspA::kan was significantly more efficient at producing biofilms than the wild-type strain, there was no significant difference in virulence between the mutant and the wild-type strains. CONCLUSION: These results demonstrate that aspA is required for bacterial growth in complex medium, and under anaerobic, acid, and iron-limited conditions.
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spelling pubmed-77133222020-12-03 Role of aspartate ammonia-lyase in Pasteurella multocida Wang, Zui Li, Li Liu, Peng Wang, Chen Lu, Qin Liu, Lina Wang, Xiaozhong Luo, Qingping Shao, Huabin BMC Microbiol Research Article BACKGROUND: Pasteurella multocida is responsible for a highly infectious and contagious disease in birds, leading to heavy economic losses in the chicken industry. However, the pathogenesis of this disease is poorly understood. We recently identified an aspartate ammonia-lyase (aspA) in P. multocida that was significantly upregulated under iron-restricted conditions, the protein of which could effectively protect chicken flocks against P. multocida. However, the functions of this gene remain unclear. In the present study, we constructed aspA mutant strain △aspA::kan and complementary strain C△aspA::kan to investigate the function of aspA in detail. RESULT: Deletion of the aspA gene in P. multocida resulted in a significant reduction in bacterial growth in LB (Luria-Bertani) and MH (Mueller-Hinton) media, which was rescued by supplementation with 20 mM fumarate. The mutant strain △aspA::kan showed significantly growth defects in anaerobic conditions and acid medium, compared with the wild-type strain. Moreover, growth of △aspA::kan was more seriously impaired than that of the wild-type strain under iron-restricted conditions, and this growth recovered after supplementation with iron ions. AspA transcription was negatively regulated by iron conditions, as demonstrated by quantitative reverse transcription-polymerase chain reaction. Although competitive index assay showed the wild-type strain outcompetes the aspA mutant strain and △aspA::kan was significantly more efficient at producing biofilms than the wild-type strain, there was no significant difference in virulence between the mutant and the wild-type strains. CONCLUSION: These results demonstrate that aspA is required for bacterial growth in complex medium, and under anaerobic, acid, and iron-limited conditions. BioMed Central 2020-12-03 /pmc/articles/PMC7713322/ /pubmed/33272193 http://dx.doi.org/10.1186/s12866-020-02049-2 Text en © The Author(s) 2020 Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
spellingShingle Research Article
Wang, Zui
Li, Li
Liu, Peng
Wang, Chen
Lu, Qin
Liu, Lina
Wang, Xiaozhong
Luo, Qingping
Shao, Huabin
Role of aspartate ammonia-lyase in Pasteurella multocida
title Role of aspartate ammonia-lyase in Pasteurella multocida
title_full Role of aspartate ammonia-lyase in Pasteurella multocida
title_fullStr Role of aspartate ammonia-lyase in Pasteurella multocida
title_full_unstemmed Role of aspartate ammonia-lyase in Pasteurella multocida
title_short Role of aspartate ammonia-lyase in Pasteurella multocida
title_sort role of aspartate ammonia-lyase in pasteurella multocida
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7713322/
https://www.ncbi.nlm.nih.gov/pubmed/33272193
http://dx.doi.org/10.1186/s12866-020-02049-2
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