Cargando…
Exploiting the Richness of Environmental Waterborne Bacterial Species to Find Natural Legionella pneumophila Competitors
Legionella pneumophila is one of the most tracked waterborne pathogens and remains an important threat to human health. Despite the use of biocides, L. pneumophila is able to persist in engineered water systems with the help of multispecies biofilms and phagocytic protists. For few years now, high-t...
Autores principales: | , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2019
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6340971/ https://www.ncbi.nlm.nih.gov/pubmed/30697209 http://dx.doi.org/10.3389/fmicb.2018.03360 |
_version_ | 1783388867190063104 |
---|---|
author | Corre, Marie-Hélène Delafont, Vincent Legrand, Anasthasia Berjeaud, Jean-Marc Verdon, Julien |
author_facet | Corre, Marie-Hélène Delafont, Vincent Legrand, Anasthasia Berjeaud, Jean-Marc Verdon, Julien |
author_sort | Corre, Marie-Hélène |
collection | PubMed |
description | Legionella pneumophila is one of the most tracked waterborne pathogens and remains an important threat to human health. Despite the use of biocides, L. pneumophila is able to persist in engineered water systems with the help of multispecies biofilms and phagocytic protists. For few years now, high-throughput sequencing methods have enabled a better understanding of microbial communities in freshwater environments. Those unexplored and complex communities compete for nutrients using antagonistic molecules as war weapons. Up to now, few of these molecules were characterized in regards of L. pneumophila sensitivity. In this context, we established, from five freshwater environments, a vast collection of culturable bacteria and investigated their ability to inhibit the growth of L. pneumophila. All bacterial isolates were classified within 4 phyla, namely Proteobacteria (179/273), Bacteroidetes (48/273), Firmicutes (43/273), and Actinobacteria (3/273) according to 16S rRNA coding sequences. Aeromonas, Bacillus, Flavobacterium, and Pseudomonas were the most abundant genera (154/273). Among the 273 isolates, 178 (65.2%) were shown to be active against L. pneumophila including 137 isolates of the four previously cited main genera. Additionally, other less represented genera depicted anti-Legionella activity such as Acinetobacter, Kluyvera, Rahnella, or Sphingobacterium. Furthermore, various inhibition diameters were observed among active isolates, ranging from 0.4 to 9 cm. Such variability suggests the presence of numerous and diverse natural compounds in the microenvironment of L. pneumophila. These molecules include both diffusible secreted compounds and volatile organic compounds, the latter being mainly produced by Pseudomonas strains. Altogether, this work sheds light on unexplored freshwater bacterial communities that could be relevant for the biological control of L. pneumophila in manmade water systems. |
format | Online Article Text |
id | pubmed-6340971 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-63409712019-01-29 Exploiting the Richness of Environmental Waterborne Bacterial Species to Find Natural Legionella pneumophila Competitors Corre, Marie-Hélène Delafont, Vincent Legrand, Anasthasia Berjeaud, Jean-Marc Verdon, Julien Front Microbiol Microbiology Legionella pneumophila is one of the most tracked waterborne pathogens and remains an important threat to human health. Despite the use of biocides, L. pneumophila is able to persist in engineered water systems with the help of multispecies biofilms and phagocytic protists. For few years now, high-throughput sequencing methods have enabled a better understanding of microbial communities in freshwater environments. Those unexplored and complex communities compete for nutrients using antagonistic molecules as war weapons. Up to now, few of these molecules were characterized in regards of L. pneumophila sensitivity. In this context, we established, from five freshwater environments, a vast collection of culturable bacteria and investigated their ability to inhibit the growth of L. pneumophila. All bacterial isolates were classified within 4 phyla, namely Proteobacteria (179/273), Bacteroidetes (48/273), Firmicutes (43/273), and Actinobacteria (3/273) according to 16S rRNA coding sequences. Aeromonas, Bacillus, Flavobacterium, and Pseudomonas were the most abundant genera (154/273). Among the 273 isolates, 178 (65.2%) were shown to be active against L. pneumophila including 137 isolates of the four previously cited main genera. Additionally, other less represented genera depicted anti-Legionella activity such as Acinetobacter, Kluyvera, Rahnella, or Sphingobacterium. Furthermore, various inhibition diameters were observed among active isolates, ranging from 0.4 to 9 cm. Such variability suggests the presence of numerous and diverse natural compounds in the microenvironment of L. pneumophila. These molecules include both diffusible secreted compounds and volatile organic compounds, the latter being mainly produced by Pseudomonas strains. Altogether, this work sheds light on unexplored freshwater bacterial communities that could be relevant for the biological control of L. pneumophila in manmade water systems. Frontiers Media S.A. 2019-01-15 /pmc/articles/PMC6340971/ /pubmed/30697209 http://dx.doi.org/10.3389/fmicb.2018.03360 Text en Copyright © 2019 Corre, Delafont, Legrand, Berjeaud and Verdon. http://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 | Microbiology Corre, Marie-Hélène Delafont, Vincent Legrand, Anasthasia Berjeaud, Jean-Marc Verdon, Julien Exploiting the Richness of Environmental Waterborne Bacterial Species to Find Natural Legionella pneumophila Competitors |
title | Exploiting the Richness of Environmental Waterborne Bacterial Species to Find Natural Legionella pneumophila Competitors |
title_full | Exploiting the Richness of Environmental Waterborne Bacterial Species to Find Natural Legionella pneumophila Competitors |
title_fullStr | Exploiting the Richness of Environmental Waterborne Bacterial Species to Find Natural Legionella pneumophila Competitors |
title_full_unstemmed | Exploiting the Richness of Environmental Waterborne Bacterial Species to Find Natural Legionella pneumophila Competitors |
title_short | Exploiting the Richness of Environmental Waterborne Bacterial Species to Find Natural Legionella pneumophila Competitors |
title_sort | exploiting the richness of environmental waterborne bacterial species to find natural legionella pneumophila competitors |
topic | Microbiology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6340971/ https://www.ncbi.nlm.nih.gov/pubmed/30697209 http://dx.doi.org/10.3389/fmicb.2018.03360 |
work_keys_str_mv | AT corremariehelene exploitingtherichnessofenvironmentalwaterbornebacterialspeciestofindnaturallegionellapneumophilacompetitors AT delafontvincent exploitingtherichnessofenvironmentalwaterbornebacterialspeciestofindnaturallegionellapneumophilacompetitors AT legrandanasthasia exploitingtherichnessofenvironmentalwaterbornebacterialspeciestofindnaturallegionellapneumophilacompetitors AT berjeaudjeanmarc exploitingtherichnessofenvironmentalwaterbornebacterialspeciestofindnaturallegionellapneumophilacompetitors AT verdonjulien exploitingtherichnessofenvironmentalwaterbornebacterialspeciestofindnaturallegionellapneumophilacompetitors |