Cargando…

Temperature-dependent virus lifecycle choices may reveal and predict facets of the biology of opportunistic pathogenic bacteria

Melioidosis, a serious illness caused by Burkholderia pseudomallei, results in up to 40% fatality in infected patients. The pathogen is found in tropical water and soil. Recent findings demonstrated that bacterial numbers can be regulated by a novel clade of phages that are abundant in soil and wate...

Descripción completa

Detalles Bibliográficos
Autores principales: Egilmez, Halil I., Morozov, Andrew Yu., Clokie, Martha R. J., Shan, Jinyu, Letarov, Andrey, Galyov, Edouard E.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6018541/
https://www.ncbi.nlm.nih.gov/pubmed/29941954
http://dx.doi.org/10.1038/s41598-018-27716-3
_version_ 1783334974366154752
author Egilmez, Halil I.
Morozov, Andrew Yu.
Clokie, Martha R. J.
Shan, Jinyu
Letarov, Andrey
Galyov, Edouard E.
author_facet Egilmez, Halil I.
Morozov, Andrew Yu.
Clokie, Martha R. J.
Shan, Jinyu
Letarov, Andrey
Galyov, Edouard E.
author_sort Egilmez, Halil I.
collection PubMed
description Melioidosis, a serious illness caused by Burkholderia pseudomallei, results in up to 40% fatality in infected patients. The pathogen is found in tropical water and soil. Recent findings demonstrated that bacterial numbers can be regulated by a novel clade of phages that are abundant in soil and water. These phages differentially infect their bacterial hosts causing lysis at high temperatures and lysogeny at lower temperatures. Thus seasonal and daily temperature variations would cause switches in phage-bacteria interactions. We developed mathematical models using realistic parameters to explore the impact of phages on B. pseudomallei populations in the surface water of rice fields over time and under seasonally changing environmental conditions. Historical records were used to provide UV radiation levels and temperature for two Thailand provinces. The models predict seasonal variation of phage-free bacterial numbers correlates with the higher risk of melioidosis acquisition during the “warm and wet” season. We find that enrichment of the environment may lead to irregular large amplitude pulses of bacterial numbers that could significantly increase the probability of disease acquisition. Our results suggest that the phages may regulate B. pseudomallei populations throughout the seasons, and these data can potentially help improve the melioidosis prevention efforts in Southeast Asia.
format Online
Article
Text
id pubmed-6018541
institution National Center for Biotechnology Information
language English
publishDate 2018
publisher Nature Publishing Group UK
record_format MEDLINE/PubMed
spelling pubmed-60185412018-07-06 Temperature-dependent virus lifecycle choices may reveal and predict facets of the biology of opportunistic pathogenic bacteria Egilmez, Halil I. Morozov, Andrew Yu. Clokie, Martha R. J. Shan, Jinyu Letarov, Andrey Galyov, Edouard E. Sci Rep Article Melioidosis, a serious illness caused by Burkholderia pseudomallei, results in up to 40% fatality in infected patients. The pathogen is found in tropical water and soil. Recent findings demonstrated that bacterial numbers can be regulated by a novel clade of phages that are abundant in soil and water. These phages differentially infect their bacterial hosts causing lysis at high temperatures and lysogeny at lower temperatures. Thus seasonal and daily temperature variations would cause switches in phage-bacteria interactions. We developed mathematical models using realistic parameters to explore the impact of phages on B. pseudomallei populations in the surface water of rice fields over time and under seasonally changing environmental conditions. Historical records were used to provide UV radiation levels and temperature for two Thailand provinces. The models predict seasonal variation of phage-free bacterial numbers correlates with the higher risk of melioidosis acquisition during the “warm and wet” season. We find that enrichment of the environment may lead to irregular large amplitude pulses of bacterial numbers that could significantly increase the probability of disease acquisition. Our results suggest that the phages may regulate B. pseudomallei populations throughout the seasons, and these data can potentially help improve the melioidosis prevention efforts in Southeast Asia. Nature Publishing Group UK 2018-06-25 /pmc/articles/PMC6018541/ /pubmed/29941954 http://dx.doi.org/10.1038/s41598-018-27716-3 Text en © The Author(s) 2018 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
Egilmez, Halil I.
Morozov, Andrew Yu.
Clokie, Martha R. J.
Shan, Jinyu
Letarov, Andrey
Galyov, Edouard E.
Temperature-dependent virus lifecycle choices may reveal and predict facets of the biology of opportunistic pathogenic bacteria
title Temperature-dependent virus lifecycle choices may reveal and predict facets of the biology of opportunistic pathogenic bacteria
title_full Temperature-dependent virus lifecycle choices may reveal and predict facets of the biology of opportunistic pathogenic bacteria
title_fullStr Temperature-dependent virus lifecycle choices may reveal and predict facets of the biology of opportunistic pathogenic bacteria
title_full_unstemmed Temperature-dependent virus lifecycle choices may reveal and predict facets of the biology of opportunistic pathogenic bacteria
title_short Temperature-dependent virus lifecycle choices may reveal and predict facets of the biology of opportunistic pathogenic bacteria
title_sort temperature-dependent virus lifecycle choices may reveal and predict facets of the biology of opportunistic pathogenic bacteria
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6018541/
https://www.ncbi.nlm.nih.gov/pubmed/29941954
http://dx.doi.org/10.1038/s41598-018-27716-3
work_keys_str_mv AT egilmezhalili temperaturedependentviruslifecyclechoicesmayrevealandpredictfacetsofthebiologyofopportunisticpathogenicbacteria
AT morozovandrewyu temperaturedependentviruslifecyclechoicesmayrevealandpredictfacetsofthebiologyofopportunisticpathogenicbacteria
AT clokiemartharj temperaturedependentviruslifecyclechoicesmayrevealandpredictfacetsofthebiologyofopportunisticpathogenicbacteria
AT shanjinyu temperaturedependentviruslifecyclechoicesmayrevealandpredictfacetsofthebiologyofopportunisticpathogenicbacteria
AT letarovandrey temperaturedependentviruslifecyclechoicesmayrevealandpredictfacetsofthebiologyofopportunisticpathogenicbacteria
AT galyovedouarde temperaturedependentviruslifecyclechoicesmayrevealandpredictfacetsofthebiologyofopportunisticpathogenicbacteria