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In-depth Analysis of IS6110 Genomic Variability in the Mycobacterium tuberculosis Complex

The insertion sequence (IS) 6110 is a repetitive mobile element specific for the Mycobacterium tuberculosis complex (MTBC) used for years to diagnose and genotype this pathogen. It contains the overlapping reading frames orfA and orfB that encode a transposase. Its genetic variability is difficult t...

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Autores principales: Comín, Jessica, Otal, Isabel, Samper, Sofía
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8912993/
https://www.ncbi.nlm.nih.gov/pubmed/35283840
http://dx.doi.org/10.3389/fmicb.2022.767912
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author Comín, Jessica
Otal, Isabel
Samper, Sofía
author_facet Comín, Jessica
Otal, Isabel
Samper, Sofía
author_sort Comín, Jessica
collection PubMed
description The insertion sequence (IS) 6110 is a repetitive mobile element specific for the Mycobacterium tuberculosis complex (MTBC) used for years to diagnose and genotype this pathogen. It contains the overlapping reading frames orfA and orfB that encode a transposase. Its genetic variability is difficult to study because multiple copies are present in the genome. IS6110 is randomly located, nevertheless some preferential locations have been reported, which could be related to the behaviour of the strains. The aim of this work was to determine the intra- and inter-strain genetic conservation of this element in the MTBC. For this purpose, we analysed 158 sequences of IS6110 copies from 55 strains. Eighty-four copies were from 17 strains for which we knew all the locations in their genome. In addition, we studied 74 IS6110 copies in 38 different MTBC strains in which the location was characteristic of different families including Haarlem, LAM, S, and L6 strains. We observed mutation in 13.3% of the copies studied and we found 10 IS6110 variants in 21 copies belonging to 16 strains. The high copy number strains showed 6.2% of their IS6110 copies mutated, in contrast with the 31.1% in the low-copy-number strains. The apparently more ancient copy localised in the DR region was that with more variant copies, probably because this was the most studied location. Notably, all Haarlem and X family strains studied have an IS6110 in Rv0403c, suggesting a common origin for both families. Nevertheless, we detected a variant specific for the X family that would have occurred in this location after the phylogenetic separation. This variant does not prevent transposition although it may occur at a lower frequency, as X strains remain with low copy number (LCN) of IS6110.
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spelling pubmed-89129932022-03-11 In-depth Analysis of IS6110 Genomic Variability in the Mycobacterium tuberculosis Complex Comín, Jessica Otal, Isabel Samper, Sofía Front Microbiol Microbiology The insertion sequence (IS) 6110 is a repetitive mobile element specific for the Mycobacterium tuberculosis complex (MTBC) used for years to diagnose and genotype this pathogen. It contains the overlapping reading frames orfA and orfB that encode a transposase. Its genetic variability is difficult to study because multiple copies are present in the genome. IS6110 is randomly located, nevertheless some preferential locations have been reported, which could be related to the behaviour of the strains. The aim of this work was to determine the intra- and inter-strain genetic conservation of this element in the MTBC. For this purpose, we analysed 158 sequences of IS6110 copies from 55 strains. Eighty-four copies were from 17 strains for which we knew all the locations in their genome. In addition, we studied 74 IS6110 copies in 38 different MTBC strains in which the location was characteristic of different families including Haarlem, LAM, S, and L6 strains. We observed mutation in 13.3% of the copies studied and we found 10 IS6110 variants in 21 copies belonging to 16 strains. The high copy number strains showed 6.2% of their IS6110 copies mutated, in contrast with the 31.1% in the low-copy-number strains. The apparently more ancient copy localised in the DR region was that with more variant copies, probably because this was the most studied location. Notably, all Haarlem and X family strains studied have an IS6110 in Rv0403c, suggesting a common origin for both families. Nevertheless, we detected a variant specific for the X family that would have occurred in this location after the phylogenetic separation. This variant does not prevent transposition although it may occur at a lower frequency, as X strains remain with low copy number (LCN) of IS6110. Frontiers Media S.A. 2022-02-24 /pmc/articles/PMC8912993/ /pubmed/35283840 http://dx.doi.org/10.3389/fmicb.2022.767912 Text en Copyright © 2022 Comín, Otal and Samper. https://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
Comín, Jessica
Otal, Isabel
Samper, Sofía
In-depth Analysis of IS6110 Genomic Variability in the Mycobacterium tuberculosis Complex
title In-depth Analysis of IS6110 Genomic Variability in the Mycobacterium tuberculosis Complex
title_full In-depth Analysis of IS6110 Genomic Variability in the Mycobacterium tuberculosis Complex
title_fullStr In-depth Analysis of IS6110 Genomic Variability in the Mycobacterium tuberculosis Complex
title_full_unstemmed In-depth Analysis of IS6110 Genomic Variability in the Mycobacterium tuberculosis Complex
title_short In-depth Analysis of IS6110 Genomic Variability in the Mycobacterium tuberculosis Complex
title_sort in-depth analysis of is6110 genomic variability in the mycobacterium tuberculosis complex
topic Microbiology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8912993/
https://www.ncbi.nlm.nih.gov/pubmed/35283840
http://dx.doi.org/10.3389/fmicb.2022.767912
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