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The Involvement of the csy1 Gene in the Antimicrobial Resistance of Acinetobacter baumannii
Acinetobacter baumannii is an important, opportunistic nosocomial pathogen that causes a variety of nosocomial infections, and whose drug resistance rate has increased in recent years. The CRISPR-Cas system exists in several bacteria, providing adaptive immunity to foreign nucleic acid invasion. Thi...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8825777/ https://www.ncbi.nlm.nih.gov/pubmed/35155494 http://dx.doi.org/10.3389/fmed.2022.797104 |
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author | Guo, Tingting Sun, Xiaoli Li, Mengying Wang, Yuhang Jiao, Hongmei Li, Guocai |
author_facet | Guo, Tingting Sun, Xiaoli Li, Mengying Wang, Yuhang Jiao, Hongmei Li, Guocai |
author_sort | Guo, Tingting |
collection | PubMed |
description | Acinetobacter baumannii is an important, opportunistic nosocomial pathogen that causes a variety of nosocomial infections, and whose drug resistance rate has increased in recent years. The CRISPR-Cas system exists in several bacteria, providing adaptive immunity to foreign nucleic acid invasion. This study explores whether CRISPR-Cas is related to drug resistance. Antibiotics were used to treat strains ATCC19606 and AB43, and the expression of CRISPR-related genes was found to be changed. The Csy proteins (Csy1–4) were previously detected to promote target recognition; however, the potential function of csy1 gene is still unknown. Thus, the Rec(Ab) homologous recombination system was utilized to knock out the csy1 gene from A. baumannii AB43, which carries the Type I-Fb CRISPR-Cas system, and to observe the drug resistance changes in wild-type and csy1-deleted strains. The AB43Δcsy1 mutant strain was found to become resistant to antibiotics, while the wild-type strain was sensitive to antibiotics. Moreover, transcriptome analysis revealed that the csy1 gene regulates genes encoding CRISPR-Cas-related proteins, drug-resistant efflux pumps, membrane proteins, and oxidative phosphorylation-related proteins, inhibiting antimicrobial resistance in A. baumannii. The in vitro resistance development assay revealed that the complete CRISPR-Cas system could inhibit the development of bacterial resistance. Our findings expand our understanding of the role of CRISPR-Cas csy1 gene in A. baumannii and link the CRISPR-Cas system to the biogenesis of bacterial drug-resistant structures. |
format | Online Article Text |
id | pubmed-8825777 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-88257772022-02-10 The Involvement of the csy1 Gene in the Antimicrobial Resistance of Acinetobacter baumannii Guo, Tingting Sun, Xiaoli Li, Mengying Wang, Yuhang Jiao, Hongmei Li, Guocai Front Med (Lausanne) Medicine Acinetobacter baumannii is an important, opportunistic nosocomial pathogen that causes a variety of nosocomial infections, and whose drug resistance rate has increased in recent years. The CRISPR-Cas system exists in several bacteria, providing adaptive immunity to foreign nucleic acid invasion. This study explores whether CRISPR-Cas is related to drug resistance. Antibiotics were used to treat strains ATCC19606 and AB43, and the expression of CRISPR-related genes was found to be changed. The Csy proteins (Csy1–4) were previously detected to promote target recognition; however, the potential function of csy1 gene is still unknown. Thus, the Rec(Ab) homologous recombination system was utilized to knock out the csy1 gene from A. baumannii AB43, which carries the Type I-Fb CRISPR-Cas system, and to observe the drug resistance changes in wild-type and csy1-deleted strains. The AB43Δcsy1 mutant strain was found to become resistant to antibiotics, while the wild-type strain was sensitive to antibiotics. Moreover, transcriptome analysis revealed that the csy1 gene regulates genes encoding CRISPR-Cas-related proteins, drug-resistant efflux pumps, membrane proteins, and oxidative phosphorylation-related proteins, inhibiting antimicrobial resistance in A. baumannii. The in vitro resistance development assay revealed that the complete CRISPR-Cas system could inhibit the development of bacterial resistance. Our findings expand our understanding of the role of CRISPR-Cas csy1 gene in A. baumannii and link the CRISPR-Cas system to the biogenesis of bacterial drug-resistant structures. Frontiers Media S.A. 2022-01-26 /pmc/articles/PMC8825777/ /pubmed/35155494 http://dx.doi.org/10.3389/fmed.2022.797104 Text en Copyright © 2022 Guo, Sun, Li, Wang, Jiao and Li. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Medicine Guo, Tingting Sun, Xiaoli Li, Mengying Wang, Yuhang Jiao, Hongmei Li, Guocai The Involvement of the csy1 Gene in the Antimicrobial Resistance of Acinetobacter baumannii |
title | The Involvement of the csy1 Gene in the Antimicrobial Resistance of Acinetobacter baumannii |
title_full | The Involvement of the csy1 Gene in the Antimicrobial Resistance of Acinetobacter baumannii |
title_fullStr | The Involvement of the csy1 Gene in the Antimicrobial Resistance of Acinetobacter baumannii |
title_full_unstemmed | The Involvement of the csy1 Gene in the Antimicrobial Resistance of Acinetobacter baumannii |
title_short | The Involvement of the csy1 Gene in the Antimicrobial Resistance of Acinetobacter baumannii |
title_sort | involvement of the csy1 gene in the antimicrobial resistance of acinetobacter baumannii |
topic | Medicine |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8825777/ https://www.ncbi.nlm.nih.gov/pubmed/35155494 http://dx.doi.org/10.3389/fmed.2022.797104 |
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