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High β-lactam resistance in Gram-negative bacteria associated with kennel cough and cat flu in Egypt

Antimicrobial resistance within pets has gained worldwide attention due to pets close contact with humans. This report examined at the molecular level, the antimicrobial resistance mechanisms associated with kennel cough and cat flu. 1378 pets in total were assessed for signs of respiratory infectio...

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Autores principales: Khalifa, Hazim O., Oreiby, Atef F., Okanda, Takashi, Kato, Yasuyuki, Matsumoto, Tetsuya
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7870956/
https://www.ncbi.nlm.nih.gov/pubmed/33558604
http://dx.doi.org/10.1038/s41598-021-82061-2
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author Khalifa, Hazim O.
Oreiby, Atef F.
Okanda, Takashi
Kato, Yasuyuki
Matsumoto, Tetsuya
author_facet Khalifa, Hazim O.
Oreiby, Atef F.
Okanda, Takashi
Kato, Yasuyuki
Matsumoto, Tetsuya
author_sort Khalifa, Hazim O.
collection PubMed
description Antimicrobial resistance within pets has gained worldwide attention due to pets close contact with humans. This report examined at the molecular level, the antimicrobial resistance mechanisms associated with kennel cough and cat flu. 1378 pets in total were assessed for signs of respiratory infection, and nasal and conjunctival swabs were collected across 76 diseased animals. Phenotypically, 27% of the isolates were characterized by multidrug resistance and possessed high levels of resistance rates to β-lactams. Phenotypic ESBLs/AmpCs production were identified within 40.5% and 24.3% of the isolates, respectively. Genotypically, ESBL- and AmpC-encoding genes were detected in 33.8% and 10.8% of the isolates, respectively, with bla(SHV) comprising the most identified ESBL, and bla(CMY) and bla(ACT) present as the AmpC with the highest levels. qnr genes were identified in 64.9% of the isolates, with qnrS being the most prevalent (44.6%). Several antimicrobial resistance determinants were detected for the first time within pets from Africa, including bla(CTX-M-37), bla(CTX-M-156), bla(SHV-11), bla(ACT-23), bla(ACT25/31), bla(DHA-1), and bla(CMY-169). Our results revealed that pets displaying symptoms of respiratory illness are potential sources for pathogenic microbes possessing unique resistance mechanisms which could be disseminated to humans, thus leading to the development of severe untreatable infections in these hosts.
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spelling pubmed-78709562021-02-10 High β-lactam resistance in Gram-negative bacteria associated with kennel cough and cat flu in Egypt Khalifa, Hazim O. Oreiby, Atef F. Okanda, Takashi Kato, Yasuyuki Matsumoto, Tetsuya Sci Rep Article Antimicrobial resistance within pets has gained worldwide attention due to pets close contact with humans. This report examined at the molecular level, the antimicrobial resistance mechanisms associated with kennel cough and cat flu. 1378 pets in total were assessed for signs of respiratory infection, and nasal and conjunctival swabs were collected across 76 diseased animals. Phenotypically, 27% of the isolates were characterized by multidrug resistance and possessed high levels of resistance rates to β-lactams. Phenotypic ESBLs/AmpCs production were identified within 40.5% and 24.3% of the isolates, respectively. Genotypically, ESBL- and AmpC-encoding genes were detected in 33.8% and 10.8% of the isolates, respectively, with bla(SHV) comprising the most identified ESBL, and bla(CMY) and bla(ACT) present as the AmpC with the highest levels. qnr genes were identified in 64.9% of the isolates, with qnrS being the most prevalent (44.6%). Several antimicrobial resistance determinants were detected for the first time within pets from Africa, including bla(CTX-M-37), bla(CTX-M-156), bla(SHV-11), bla(ACT-23), bla(ACT25/31), bla(DHA-1), and bla(CMY-169). Our results revealed that pets displaying symptoms of respiratory illness are potential sources for pathogenic microbes possessing unique resistance mechanisms which could be disseminated to humans, thus leading to the development of severe untreatable infections in these hosts. Nature Publishing Group UK 2021-02-08 /pmc/articles/PMC7870956/ /pubmed/33558604 http://dx.doi.org/10.1038/s41598-021-82061-2 Text en © The Author(s) 2021 Open Access This 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/.
spellingShingle Article
Khalifa, Hazim O.
Oreiby, Atef F.
Okanda, Takashi
Kato, Yasuyuki
Matsumoto, Tetsuya
High β-lactam resistance in Gram-negative bacteria associated with kennel cough and cat flu in Egypt
title High β-lactam resistance in Gram-negative bacteria associated with kennel cough and cat flu in Egypt
title_full High β-lactam resistance in Gram-negative bacteria associated with kennel cough and cat flu in Egypt
title_fullStr High β-lactam resistance in Gram-negative bacteria associated with kennel cough and cat flu in Egypt
title_full_unstemmed High β-lactam resistance in Gram-negative bacteria associated with kennel cough and cat flu in Egypt
title_short High β-lactam resistance in Gram-negative bacteria associated with kennel cough and cat flu in Egypt
title_sort high β-lactam resistance in gram-negative bacteria associated with kennel cough and cat flu in egypt
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7870956/
https://www.ncbi.nlm.nih.gov/pubmed/33558604
http://dx.doi.org/10.1038/s41598-021-82061-2
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