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Heterogeneity among Homologs of Cutinase-Like Protein Cut5 in Mycobacteria

The study of genomic variability within various pathogenic and non-pathogenic strains of mycobacteria provides insight into their evolution and pathogenesis. The mycobacterial genome encodes seven cutinase-like proteins and each one of these exhibit distinct characteristics. We describe the presence...

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Autores principales: Verma, Deepshikha, Das, Lahari, Gambhir, Vandana, Dikshit, Kanak Lata, Varshney, Grish C.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4503659/
https://www.ncbi.nlm.nih.gov/pubmed/26177502
http://dx.doi.org/10.1371/journal.pone.0133186
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author Verma, Deepshikha
Das, Lahari
Gambhir, Vandana
Dikshit, Kanak Lata
Varshney, Grish C.
author_facet Verma, Deepshikha
Das, Lahari
Gambhir, Vandana
Dikshit, Kanak Lata
Varshney, Grish C.
author_sort Verma, Deepshikha
collection PubMed
description The study of genomic variability within various pathogenic and non-pathogenic strains of mycobacteria provides insight into their evolution and pathogenesis. The mycobacterial genome encodes seven cutinase-like proteins and each one of these exhibit distinct characteristics. We describe the presence of Cut5, a member of the cutinase family, in mycobacteria and the existence of a unique genomic arrangement in the cut5 gene of M. tuberculosis (Mtb) strains. A single nucleotide (T) insertion is observed in the cut5 gene, which is specific for Mtb strains. Using in silico analysis and RT-PCR, we demonstrate the transcription of Rv3724/cut5 as Rv3724a/cut5a and Rv3724b/cut5b in Mtb H37Rv and as full length cut5 in M. bovis. Cut5b protein of Mtb H37Rv (MtbCut5b) was found to be antigenically similar to its homologs in M. bovis and M. smegmatis, without any observed cross-reactivity with other Mtb cutinases. Also, the presence of Cut5b in Mtb and its homologs in M. bovis and M. smegmatis were confirmed by western blotting using antibodies raised against recombinant Cut5b. In Mtb H37Rv, Cut5b was found to be localized in the cell wall, cytosol and membrane fractions. We also report the vast prevalence of Cut5 homologs in pathogenic and non pathogenic species of mycobacteria. In silico analysis revealed that this protein has three possible organizations in mycobacteria. Also, a single nucleotide (T) insertion in Mtb strains and varied genomic arrangements within mycobacterial species make Rv3724/Cut5 a potential candidate that can be exploited as a biomarker in Mtb infection.
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spelling pubmed-45036592015-07-17 Heterogeneity among Homologs of Cutinase-Like Protein Cut5 in Mycobacteria Verma, Deepshikha Das, Lahari Gambhir, Vandana Dikshit, Kanak Lata Varshney, Grish C. PLoS One Research Article The study of genomic variability within various pathogenic and non-pathogenic strains of mycobacteria provides insight into their evolution and pathogenesis. The mycobacterial genome encodes seven cutinase-like proteins and each one of these exhibit distinct characteristics. We describe the presence of Cut5, a member of the cutinase family, in mycobacteria and the existence of a unique genomic arrangement in the cut5 gene of M. tuberculosis (Mtb) strains. A single nucleotide (T) insertion is observed in the cut5 gene, which is specific for Mtb strains. Using in silico analysis and RT-PCR, we demonstrate the transcription of Rv3724/cut5 as Rv3724a/cut5a and Rv3724b/cut5b in Mtb H37Rv and as full length cut5 in M. bovis. Cut5b protein of Mtb H37Rv (MtbCut5b) was found to be antigenically similar to its homologs in M. bovis and M. smegmatis, without any observed cross-reactivity with other Mtb cutinases. Also, the presence of Cut5b in Mtb and its homologs in M. bovis and M. smegmatis were confirmed by western blotting using antibodies raised against recombinant Cut5b. In Mtb H37Rv, Cut5b was found to be localized in the cell wall, cytosol and membrane fractions. We also report the vast prevalence of Cut5 homologs in pathogenic and non pathogenic species of mycobacteria. In silico analysis revealed that this protein has three possible organizations in mycobacteria. Also, a single nucleotide (T) insertion in Mtb strains and varied genomic arrangements within mycobacterial species make Rv3724/Cut5 a potential candidate that can be exploited as a biomarker in Mtb infection. Public Library of Science 2015-07-15 /pmc/articles/PMC4503659/ /pubmed/26177502 http://dx.doi.org/10.1371/journal.pone.0133186 Text en © 2015 Verma et al http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Verma, Deepshikha
Das, Lahari
Gambhir, Vandana
Dikshit, Kanak Lata
Varshney, Grish C.
Heterogeneity among Homologs of Cutinase-Like Protein Cut5 in Mycobacteria
title Heterogeneity among Homologs of Cutinase-Like Protein Cut5 in Mycobacteria
title_full Heterogeneity among Homologs of Cutinase-Like Protein Cut5 in Mycobacteria
title_fullStr Heterogeneity among Homologs of Cutinase-Like Protein Cut5 in Mycobacteria
title_full_unstemmed Heterogeneity among Homologs of Cutinase-Like Protein Cut5 in Mycobacteria
title_short Heterogeneity among Homologs of Cutinase-Like Protein Cut5 in Mycobacteria
title_sort heterogeneity among homologs of cutinase-like protein cut5 in mycobacteria
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4503659/
https://www.ncbi.nlm.nih.gov/pubmed/26177502
http://dx.doi.org/10.1371/journal.pone.0133186
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