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Genome Analysis of an Enterococcal Prophage, Entfac.MY
BACKGROUND: Bacteriophages are bacterial parasites. Unlike lytic bacteriophages, lysogenic bacteriophages do not multiply immediately after entering the host cells and may integrate their genomes into the bacterial genomes as prophages. Prophages can include various phenotypic and genotypic effects...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Avicenna Research Institute
2022
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9376991/ https://www.ncbi.nlm.nih.gov/pubmed/36061127 http://dx.doi.org/10.18502/ajmb.v14i3.9826 |
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author | Yazdanizad, Maryam Mazaheri Nezhad Fard, Ramin Javdani Shahedin, Golshid Salehi, Mohammadreza Dumanloo, Mahsa Saboor Yaraghi, Ali Akbar |
author_facet | Yazdanizad, Maryam Mazaheri Nezhad Fard, Ramin Javdani Shahedin, Golshid Salehi, Mohammadreza Dumanloo, Mahsa Saboor Yaraghi, Ali Akbar |
author_sort | Yazdanizad, Maryam |
collection | PubMed |
description | BACKGROUND: Bacteriophages are bacterial parasites. Unlike lytic bacteriophages, lysogenic bacteriophages do not multiply immediately after entering the host cells and may integrate their genomes into the bacterial genomes as prophages. Prophages can include various phenotypic and genotypic effects on the host bacteria. Enterococcus spp. are Gram-positive bacteria that cause infections in humans and animals. In recent decades, these bacteria have become resistant to various antimicrobials, including vancomycin. The aim of this study was to analyze genome of an enterococcal prophage. METHODS: In this study, Enterococcus faecium EntfacYE was isolated from biological samples and its genome was analyzed using next-generation sequencing method. RESULTS: Overall, 254 prophage genes were identified in the bacterial genome. The prophage included 39 housekeeping, 41 replication and regulation, 80 structural and packaging, and 48 lysis genes. Moreover, 46 genes with unknown functions were identified. All genes were annotated in DNA Data Bank of Japan. CONCLUSION: In general, most prophage genes were linked to packaging and structure (31.5%) gene group. However, genes with unknown functions included a high proportion (18.11%), which indicated necessity of further analyses. Genomic analysis of the prophages can be effective in better understanding of their roles in development of bacterial resistance to antibiotics. Moreover, identification and study of prophages can help researchers develop genetic engineering tools and novel infection therapies. |
format | Online Article Text |
id | pubmed-9376991 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Avicenna Research Institute |
record_format | MEDLINE/PubMed |
spelling | pubmed-93769912022-09-01 Genome Analysis of an Enterococcal Prophage, Entfac.MY Yazdanizad, Maryam Mazaheri Nezhad Fard, Ramin Javdani Shahedin, Golshid Salehi, Mohammadreza Dumanloo, Mahsa Saboor Yaraghi, Ali Akbar Avicenna J Med Biotechnol Original Article BACKGROUND: Bacteriophages are bacterial parasites. Unlike lytic bacteriophages, lysogenic bacteriophages do not multiply immediately after entering the host cells and may integrate their genomes into the bacterial genomes as prophages. Prophages can include various phenotypic and genotypic effects on the host bacteria. Enterococcus spp. are Gram-positive bacteria that cause infections in humans and animals. In recent decades, these bacteria have become resistant to various antimicrobials, including vancomycin. The aim of this study was to analyze genome of an enterococcal prophage. METHODS: In this study, Enterococcus faecium EntfacYE was isolated from biological samples and its genome was analyzed using next-generation sequencing method. RESULTS: Overall, 254 prophage genes were identified in the bacterial genome. The prophage included 39 housekeeping, 41 replication and regulation, 80 structural and packaging, and 48 lysis genes. Moreover, 46 genes with unknown functions were identified. All genes were annotated in DNA Data Bank of Japan. CONCLUSION: In general, most prophage genes were linked to packaging and structure (31.5%) gene group. However, genes with unknown functions included a high proportion (18.11%), which indicated necessity of further analyses. Genomic analysis of the prophages can be effective in better understanding of their roles in development of bacterial resistance to antibiotics. Moreover, identification and study of prophages can help researchers develop genetic engineering tools and novel infection therapies. Avicenna Research Institute 2022 /pmc/articles/PMC9376991/ /pubmed/36061127 http://dx.doi.org/10.18502/ajmb.v14i3.9826 Text en Copyright© 2022 Avicenna Research Institute https://creativecommons.org/licenses/by-nc/4.0/This is an open access article distributed in accordance with the Creative Commons Attribution Non Commercial (CC BY-NC 4.0) license, which permits others to distribute, remix, adapt, build upon this work non-commercially, and license their derivative works on different terms, provided the original work is properly cited, appropriate credit is given, any changes made indicated, and the use is non-commercial. See: http://creativecommons.org/licenses/by-nc/4.0/ (https://creativecommons.org/licenses/by-nc/4.0/) |
spellingShingle | Original Article Yazdanizad, Maryam Mazaheri Nezhad Fard, Ramin Javdani Shahedin, Golshid Salehi, Mohammadreza Dumanloo, Mahsa Saboor Yaraghi, Ali Akbar Genome Analysis of an Enterococcal Prophage, Entfac.MY |
title | Genome Analysis of an Enterococcal Prophage, Entfac.MY |
title_full | Genome Analysis of an Enterococcal Prophage, Entfac.MY |
title_fullStr | Genome Analysis of an Enterococcal Prophage, Entfac.MY |
title_full_unstemmed | Genome Analysis of an Enterococcal Prophage, Entfac.MY |
title_short | Genome Analysis of an Enterococcal Prophage, Entfac.MY |
title_sort | genome analysis of an enterococcal prophage, entfac.my |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9376991/ https://www.ncbi.nlm.nih.gov/pubmed/36061127 http://dx.doi.org/10.18502/ajmb.v14i3.9826 |
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