Prospecting Environmental Mycobacteria: Combined Molecular Approaches Reveal Unprecedented Diversity

Environmental mycobacteria (EM) include species commonly found in various terrestrial and aquatic environments, encompassing animal and human pathogens in addition to saprophytes. Approximately 150 EM species can be separated into fast and slow growers based on sequence and copy number differences o...

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Veröffentlicht in:PloS one 2013-07, Vol.8 (7), p.e68648-e68648
Hauptverfasser: Pontiroli, Alessandra, Khera, Tanya T, Oakley, Brian B, Mason, Sam, Dowd, Scot E, Travis, Emma R, Erenso, Girum, Aseffa, Abraham, Courtenay, Orin, Wellington, Elizabeth M. H, Hoshino, Yoshihiko
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container_issue 7
container_start_page e68648
container_title PloS one
container_volume 8
creator Pontiroli, Alessandra
Khera, Tanya T
Oakley, Brian B
Mason, Sam
Dowd, Scot E
Travis, Emma R
Erenso, Girum
Aseffa, Abraham
Courtenay, Orin
Wellington, Elizabeth M. H
Hoshino, Yoshihiko
description Environmental mycobacteria (EM) include species commonly found in various terrestrial and aquatic environments, encompassing animal and human pathogens in addition to saprophytes. Approximately 150 EM species can be separated into fast and slow growers based on sequence and copy number differences of their 16S rRNA genes. Cultivation methods are not appropriate for diversity studies; few studies have investigated EM diversity in soil despite their importance as potential reservoirs of pathogens and their hypothesized role in masking or blocking M. bovis BCG vaccine. We report here the development, optimization and validation of molecular assays targeting the 16S rRNA gene to assess diversity and prevalence of fast and slow growing EM in representative soils from semi tropical and temperate areas. New primer sets were designed also to target uniquely slow growing mycobacteria and used with PCR-DGGE, tag-encoded Titanium amplicon pyrosequencing and quantitative PCR. PCR-DGGE and pyrosequencing provided a consensus of EM diversity; for example, a high abundance of pyrosequencing reads and DGGE bands corresponded to M. moriokaense , M. colombiense and M. riyadhense . As expected pyrosequencing provided more comprehensive information; additional prevalent species included M. chlorophenolicum, M. neglectum, M. gordonae, M. aemonae . Prevalence of the total Mycobacterium genus in the soil samples ranged from 2.3×10 7 to 2.7×10 8 gene targets g −1 ; slow growers prevalence from 2.9×10 5 to 1.2×10 7 cells g −1 . This combined molecular approach enabled an unprecedented qualitative and quantitative assessment of EM across soil samples. Good concordance was found between methods and the bioinformatics analysis was validated by random resampling. Sequences from most pathogenic groups associated with slow growth were identified in extenso in all soils tested with a specific assay, allowing to unmask them from the Mycobacterium whole genus, in which, as minority members, they would have remained undetected.
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H</au><au>Hoshino, Yoshihiko</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Prospecting Environmental Mycobacteria: Combined Molecular Approaches Reveal Unprecedented Diversity</atitle><jtitle>PloS one</jtitle><addtitle>PLoS One</addtitle><date>2013-07-18</date><risdate>2013</risdate><volume>8</volume><issue>7</issue><spage>e68648</spage><epage>e68648</epage><pages>e68648-e68648</pages><issn>1932-6203</issn><eissn>1932-6203</eissn><abstract>Environmental mycobacteria (EM) include species commonly found in various terrestrial and aquatic environments, encompassing animal and human pathogens in addition to saprophytes. Approximately 150 EM species can be separated into fast and slow growers based on sequence and copy number differences of their 16S rRNA genes. Cultivation methods are not appropriate for diversity studies; few studies have investigated EM diversity in soil despite their importance as potential reservoirs of pathogens and their hypothesized role in masking or blocking M. bovis BCG vaccine. We report here the development, optimization and validation of molecular assays targeting the 16S rRNA gene to assess diversity and prevalence of fast and slow growing EM in representative soils from semi tropical and temperate areas. New primer sets were designed also to target uniquely slow growing mycobacteria and used with PCR-DGGE, tag-encoded Titanium amplicon pyrosequencing and quantitative PCR. PCR-DGGE and pyrosequencing provided a consensus of EM diversity; for example, a high abundance of pyrosequencing reads and DGGE bands corresponded to M. moriokaense , M. colombiense and M. riyadhense . As expected pyrosequencing provided more comprehensive information; additional prevalent species included M. chlorophenolicum, M. neglectum, M. gordonae, M. aemonae . Prevalence of the total Mycobacterium genus in the soil samples ranged from 2.3×10 7 to 2.7×10 8 gene targets g −1 ; slow growers prevalence from 2.9×10 5 to 1.2×10 7 cells g −1 . This combined molecular approach enabled an unprecedented qualitative and quantitative assessment of EM across soil samples. Good concordance was found between methods and the bioinformatics analysis was validated by random resampling. Sequences from most pathogenic groups associated with slow growth were identified in extenso in all soils tested with a specific assay, allowing to unmask them from the Mycobacterium whole genus, in which, as minority members, they would have remained undetected.</abstract><cop>United States</cop><pub>Public Library of Science</pub><pmid>23874704</pmid><doi>10.1371/journal.pone.0068648</doi><tpages>e68648</tpages><oa>free_for_read</oa></addata></record>
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1932-6203
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subjects Agriculture
Analysis
Aquatic animals
Aquatic environment
Bacillus Calmette-Guerin vaccine
Bacteriology
Base Sequence
BCG
BCG vaccine
Biodiversity
Bioinformatics
Biology
Climate
Computational Biology
Copy number
Cultivation
Denaturing Gradient Gel Electrophoresis
Deoxyribonucleic acid
DNA
DNA primers
DNA Primers - genetics
Ecology
Ethiopia
genes
Life sciences
Masking
Medicine
Methods
Molecular Sequence Data
Mycobacterium
Mycobacterium - genetics
Mycobacterium avium
Optimization
Pathogens
Phylogenetics
Phylogeny
Prospecting
quantitative polymerase chain reaction
Real-Time Polymerase Chain Reaction - methods
Resampling
ribosomal RNA
RNA
RNA, Ribosomal, 16S - genetics
rRNA 16S
Saprophytes
sequence analysis
Sequence Analysis, DNA
soil
Soil investigations
Soil Microbiology
Soils
Species
Species diversity
Species Specificity
Studies
temperate zones
Terrestrial environments
Tuberculosis
title Prospecting Environmental Mycobacteria: Combined Molecular Approaches Reveal Unprecedented Diversity
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