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Molecular characterization and amplified ribosomal DNA restriction analysis of entomopathogenic bacteria associated with Rhabditis (Oscheius) spp.
Bacterial strains associated with entomopathogenic nematodes (EPNs) Rhabditis (Oscheius) spp. were isolated from infected cadavers of Galleria mellonella. The obtained 18 isolates were subdivided into nine phylogenetically different genera based on comparative sequence analysis of their 16S rRNA gen...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Springer Berlin Heidelberg
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4713396/ https://www.ncbi.nlm.nih.gov/pubmed/28330100 http://dx.doi.org/10.1007/s13205-015-0326-1 |
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author | Sangeetha, Balakrishnan Geetha Jayaprakas, Cheruvandasseri Arumughan Siji, Jinachandrannair Vijayakumari Rajitha, Moochattil Shyni, Basheerkutty Mohandas, Chellappan |
author_facet | Sangeetha, Balakrishnan Geetha Jayaprakas, Cheruvandasseri Arumughan Siji, Jinachandrannair Vijayakumari Rajitha, Moochattil Shyni, Basheerkutty Mohandas, Chellappan |
author_sort | Sangeetha, Balakrishnan Geetha |
collection | PubMed |
description | Bacterial strains associated with entomopathogenic nematodes (EPNs) Rhabditis (Oscheius) spp. were isolated from infected cadavers of Galleria mellonella. The obtained 18 isolates were subdivided into nine phylogenetically different genera based on comparative sequence analysis of their 16S rRNA genes. The isolates were affiliated to three different class namely γ-proteobacteria (Enterobacter, Proteus, Providencia, Pseudomonas, Stenotrophomonas), β-proteobacteria (Alcaligenes) and Bacilli (Bacillus, Enterococcus, Lysinibacillus). It was observed that Gram-positive strains (Bacilli) were more frequently associated with the EPN, whereas Gram-negative isolates were affiliated to six different genera with more genotypic diversity. Subsequently, all bacterial isolates used in this study were analyzed by amplified ribosomal DNA restriction analysis (ARDRA). Eight restriction endonucleases (CfoI, HinfI, RsaI, DdeI, Sau3AI, AluI, HaeIII, and MspI) were examined and a total of 15 different genotypes were obtained, forming two heterogenous main clusters after analysis by un-weighted pair-group method using arithmetic averages. |
format | Online Article Text |
id | pubmed-4713396 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Springer Berlin Heidelberg |
record_format | MEDLINE/PubMed |
spelling | pubmed-47133962016-01-19 Molecular characterization and amplified ribosomal DNA restriction analysis of entomopathogenic bacteria associated with Rhabditis (Oscheius) spp. Sangeetha, Balakrishnan Geetha Jayaprakas, Cheruvandasseri Arumughan Siji, Jinachandrannair Vijayakumari Rajitha, Moochattil Shyni, Basheerkutty Mohandas, Chellappan 3 Biotech Original Article Bacterial strains associated with entomopathogenic nematodes (EPNs) Rhabditis (Oscheius) spp. were isolated from infected cadavers of Galleria mellonella. The obtained 18 isolates were subdivided into nine phylogenetically different genera based on comparative sequence analysis of their 16S rRNA genes. The isolates were affiliated to three different class namely γ-proteobacteria (Enterobacter, Proteus, Providencia, Pseudomonas, Stenotrophomonas), β-proteobacteria (Alcaligenes) and Bacilli (Bacillus, Enterococcus, Lysinibacillus). It was observed that Gram-positive strains (Bacilli) were more frequently associated with the EPN, whereas Gram-negative isolates were affiliated to six different genera with more genotypic diversity. Subsequently, all bacterial isolates used in this study were analyzed by amplified ribosomal DNA restriction analysis (ARDRA). Eight restriction endonucleases (CfoI, HinfI, RsaI, DdeI, Sau3AI, AluI, HaeIII, and MspI) were examined and a total of 15 different genotypes were obtained, forming two heterogenous main clusters after analysis by un-weighted pair-group method using arithmetic averages. Springer Berlin Heidelberg 2016-01-14 2016-06 /pmc/articles/PMC4713396/ /pubmed/28330100 http://dx.doi.org/10.1007/s13205-015-0326-1 Text en © The Author(s) 2016 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided 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. |
spellingShingle | Original Article Sangeetha, Balakrishnan Geetha Jayaprakas, Cheruvandasseri Arumughan Siji, Jinachandrannair Vijayakumari Rajitha, Moochattil Shyni, Basheerkutty Mohandas, Chellappan Molecular characterization and amplified ribosomal DNA restriction analysis of entomopathogenic bacteria associated with Rhabditis (Oscheius) spp. |
title | Molecular characterization and amplified ribosomal DNA restriction analysis of entomopathogenic bacteria associated with Rhabditis (Oscheius) spp. |
title_full | Molecular characterization and amplified ribosomal DNA restriction analysis of entomopathogenic bacteria associated with Rhabditis (Oscheius) spp. |
title_fullStr | Molecular characterization and amplified ribosomal DNA restriction analysis of entomopathogenic bacteria associated with Rhabditis (Oscheius) spp. |
title_full_unstemmed | Molecular characterization and amplified ribosomal DNA restriction analysis of entomopathogenic bacteria associated with Rhabditis (Oscheius) spp. |
title_short | Molecular characterization and amplified ribosomal DNA restriction analysis of entomopathogenic bacteria associated with Rhabditis (Oscheius) spp. |
title_sort | molecular characterization and amplified ribosomal dna restriction analysis of entomopathogenic bacteria associated with rhabditis (oscheius) spp. |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4713396/ https://www.ncbi.nlm.nih.gov/pubmed/28330100 http://dx.doi.org/10.1007/s13205-015-0326-1 |
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