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Unravelling the consequences of the bacteriophages in human samples
Bacteriophages are abundant in human biomes and therefore in human clinical samples. Although this is usually not considered, they might interfere with the recovery of bacterial pathogens at two levels: 1) by propagating in the enrichment cultures used to isolate the infectious agent, causing the ly...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7174282/ https://www.ncbi.nlm.nih.gov/pubmed/32317653 http://dx.doi.org/10.1038/s41598-020-63432-7 |
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author | Blanco-Picazo, Pedro Fernández-Orth, Dietmar Brown-Jaque, Maryury Miró, Elisenda Espinal, Paula Rodríguez-Rubio, Lorena Muniesa, Maite Navarro, Ferran |
author_facet | Blanco-Picazo, Pedro Fernández-Orth, Dietmar Brown-Jaque, Maryury Miró, Elisenda Espinal, Paula Rodríguez-Rubio, Lorena Muniesa, Maite Navarro, Ferran |
author_sort | Blanco-Picazo, Pedro |
collection | PubMed |
description | Bacteriophages are abundant in human biomes and therefore in human clinical samples. Although this is usually not considered, they might interfere with the recovery of bacterial pathogens at two levels: 1) by propagating in the enrichment cultures used to isolate the infectious agent, causing the lysis of the bacterial host and 2) by the detection of bacterial genes inside the phage capsids that mislead the presence of the bacterial pathogen. To unravel these interferences, human samples (n = 271) were analyzed and infectious phages were observed in 11% of blood culture, 28% of serum, 45% of ascitic fluid, 14% of cerebrospinal fluid and 23% of urine samples. The genetic content of phage particles from a pool of urine and ascitic fluid samples corresponded to bacteriophages infecting different bacterial genera. In addition, many bacterial genes packaged in the phage capsids, including antibiotic resistance genes and 16S rRNA genes, were detected in the viromes. Phage interference can be minimized applying a simple procedure that reduced the content of phages up to 3 logs while maintaining the bacterial load. This method reduced the detection of phage genes avoiding the interference with molecular detection of bacteria and reduced the phage propagation in the cultures, enhancing the recovery of bacteria up to 6 logs. |
format | Online Article Text |
id | pubmed-7174282 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-71742822020-04-24 Unravelling the consequences of the bacteriophages in human samples Blanco-Picazo, Pedro Fernández-Orth, Dietmar Brown-Jaque, Maryury Miró, Elisenda Espinal, Paula Rodríguez-Rubio, Lorena Muniesa, Maite Navarro, Ferran Sci Rep Article Bacteriophages are abundant in human biomes and therefore in human clinical samples. Although this is usually not considered, they might interfere with the recovery of bacterial pathogens at two levels: 1) by propagating in the enrichment cultures used to isolate the infectious agent, causing the lysis of the bacterial host and 2) by the detection of bacterial genes inside the phage capsids that mislead the presence of the bacterial pathogen. To unravel these interferences, human samples (n = 271) were analyzed and infectious phages were observed in 11% of blood culture, 28% of serum, 45% of ascitic fluid, 14% of cerebrospinal fluid and 23% of urine samples. The genetic content of phage particles from a pool of urine and ascitic fluid samples corresponded to bacteriophages infecting different bacterial genera. In addition, many bacterial genes packaged in the phage capsids, including antibiotic resistance genes and 16S rRNA genes, were detected in the viromes. Phage interference can be minimized applying a simple procedure that reduced the content of phages up to 3 logs while maintaining the bacterial load. This method reduced the detection of phage genes avoiding the interference with molecular detection of bacteria and reduced the phage propagation in the cultures, enhancing the recovery of bacteria up to 6 logs. Nature Publishing Group UK 2020-04-21 /pmc/articles/PMC7174282/ /pubmed/32317653 http://dx.doi.org/10.1038/s41598-020-63432-7 Text en © The Author(s) 2020 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 license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license 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 license, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Blanco-Picazo, Pedro Fernández-Orth, Dietmar Brown-Jaque, Maryury Miró, Elisenda Espinal, Paula Rodríguez-Rubio, Lorena Muniesa, Maite Navarro, Ferran Unravelling the consequences of the bacteriophages in human samples |
title | Unravelling the consequences of the bacteriophages in human samples |
title_full | Unravelling the consequences of the bacteriophages in human samples |
title_fullStr | Unravelling the consequences of the bacteriophages in human samples |
title_full_unstemmed | Unravelling the consequences of the bacteriophages in human samples |
title_short | Unravelling the consequences of the bacteriophages in human samples |
title_sort | unravelling the consequences of the bacteriophages in human samples |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7174282/ https://www.ncbi.nlm.nih.gov/pubmed/32317653 http://dx.doi.org/10.1038/s41598-020-63432-7 |
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