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Metagenome analyses of corroded concrete wastewater pipe biofilms reveal a complex microbial system
BACKGROUND: Concrete corrosion of wastewater collection systems is a significant cause of deterioration and premature collapse. Failure to adequately address the deteriorating infrastructure networks threatens our environment, public health, and safety. Analysis of whole-metagenome pyrosequencing da...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2012
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3409016/ https://www.ncbi.nlm.nih.gov/pubmed/22727216 http://dx.doi.org/10.1186/1471-2180-12-122 |
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author | Gomez-Alvarez, Vicente Revetta, Randy P Domingo, Jorge W Santo |
author_facet | Gomez-Alvarez, Vicente Revetta, Randy P Domingo, Jorge W Santo |
author_sort | Gomez-Alvarez, Vicente |
collection | PubMed |
description | BACKGROUND: Concrete corrosion of wastewater collection systems is a significant cause of deterioration and premature collapse. Failure to adequately address the deteriorating infrastructure networks threatens our environment, public health, and safety. Analysis of whole-metagenome pyrosequencing data and 16S rRNA gene clone libraries was used to determine microbial composition and functional genes associated with biomass harvested from crown (top) and invert (bottom) sections of a corroded wastewater pipe. RESULTS: Taxonomic and functional analysis demonstrated that approximately 90% of the total diversity was associated with the phyla Actinobacteria, Bacteroidetes, Firmicutes and Proteobacteria. The top (TP) and bottom pipe (BP) communities were different in composition, with some of the differences attributed to the abundance of sulfide-oxidizing and sulfate-reducing bacteria. Additionally, human fecal bacteria were more abundant in the BP communities. Among the functional categories, proteins involved in sulfur and nitrogen metabolism showed the most significant differences between biofilms. There was also an enrichment of genes associated with heavy metal resistance, virulence (protein secretion systems) and stress response in the TP biofilm, while a higher number of genes related to motility and chemotaxis were identified in the BP biofilm. Both biofilms contain a high number of genes associated with resistance to antibiotics and toxic compounds subsystems. CONCLUSIONS: The function potential of wastewater biofilms was highly diverse with level of COG diversity similar to that described for soil. On the basis of the metagenomic data, some factors that may contribute to niche differentiation were pH, aerobic conditions and availability of substrate, such as nitrogen and sulfur. The results from this study will help us better understand the genetic network and functional capability of microbial members of wastewater concrete biofilms. |
format | Online Article Text |
id | pubmed-3409016 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2012 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-34090162012-08-01 Metagenome analyses of corroded concrete wastewater pipe biofilms reveal a complex microbial system Gomez-Alvarez, Vicente Revetta, Randy P Domingo, Jorge W Santo BMC Microbiol Research Article BACKGROUND: Concrete corrosion of wastewater collection systems is a significant cause of deterioration and premature collapse. Failure to adequately address the deteriorating infrastructure networks threatens our environment, public health, and safety. Analysis of whole-metagenome pyrosequencing data and 16S rRNA gene clone libraries was used to determine microbial composition and functional genes associated with biomass harvested from crown (top) and invert (bottom) sections of a corroded wastewater pipe. RESULTS: Taxonomic and functional analysis demonstrated that approximately 90% of the total diversity was associated with the phyla Actinobacteria, Bacteroidetes, Firmicutes and Proteobacteria. The top (TP) and bottom pipe (BP) communities were different in composition, with some of the differences attributed to the abundance of sulfide-oxidizing and sulfate-reducing bacteria. Additionally, human fecal bacteria were more abundant in the BP communities. Among the functional categories, proteins involved in sulfur and nitrogen metabolism showed the most significant differences between biofilms. There was also an enrichment of genes associated with heavy metal resistance, virulence (protein secretion systems) and stress response in the TP biofilm, while a higher number of genes related to motility and chemotaxis were identified in the BP biofilm. Both biofilms contain a high number of genes associated with resistance to antibiotics and toxic compounds subsystems. CONCLUSIONS: The function potential of wastewater biofilms was highly diverse with level of COG diversity similar to that described for soil. On the basis of the metagenomic data, some factors that may contribute to niche differentiation were pH, aerobic conditions and availability of substrate, such as nitrogen and sulfur. The results from this study will help us better understand the genetic network and functional capability of microbial members of wastewater concrete biofilms. BioMed Central 2012-06-22 /pmc/articles/PMC3409016/ /pubmed/22727216 http://dx.doi.org/10.1186/1471-2180-12-122 Text en Copyright ©2012 Gomez-Alvarez et al.; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Article Gomez-Alvarez, Vicente Revetta, Randy P Domingo, Jorge W Santo Metagenome analyses of corroded concrete wastewater pipe biofilms reveal a complex microbial system |
title | Metagenome analyses of corroded concrete wastewater pipe biofilms reveal a complex microbial system |
title_full | Metagenome analyses of corroded concrete wastewater pipe biofilms reveal a complex microbial system |
title_fullStr | Metagenome analyses of corroded concrete wastewater pipe biofilms reveal a complex microbial system |
title_full_unstemmed | Metagenome analyses of corroded concrete wastewater pipe biofilms reveal a complex microbial system |
title_short | Metagenome analyses of corroded concrete wastewater pipe biofilms reveal a complex microbial system |
title_sort | metagenome analyses of corroded concrete wastewater pipe biofilms reveal a complex microbial system |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3409016/ https://www.ncbi.nlm.nih.gov/pubmed/22727216 http://dx.doi.org/10.1186/1471-2180-12-122 |
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