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

被引:7
作者
Comin, Jessica [1 ,2 ]
Otal, Isabel [2 ,3 ,4 ]
Samper, Sofia [1 ,2 ,4 ]
机构
[1] Hosp Univ Miguel Servet, Inst Aragones Ciencias Salud, Unidad Invest Traslac, Zaragoza, Spain
[2] Fdn IIS Aragon, Zaragoza, Spain
[3] Univ Zaragoza, Fac Med, Zaragoza, Spain
[4] CIBER Enfermedades Resp, Madrid, Spain
关键词
tuberculosis; IS6110; Mycobacterium tuberculosis complex; IS6110 genomic variability; tuberculosis evolution; PREFERENTIAL LOCUS; INSERTION-SEQUENCE; REGION; POLYMORPHISM; VIRULENCE; ELEMENTS; STRAINS; SINGLE; MOBILE;
D O I
10.3389/fmicb.2022.767912
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
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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页数:11
相关论文
共 38 条
[1]   Deciphering the role of IS6110 in a highly transmissible Mycobacterium tuberculosis Beijing strain, GC1237 [J].
Alonso, Henar ;
Ignacio Aguilo, Juan ;
Samper, Sofia ;
Antonio Caminero, Jose ;
Isolina Campos-Herrero, Maria ;
Gicquel, Brigitte ;
Brosch, Roland ;
Martin, Carlos ;
Otal, Isabel .
TUBERCULOSIS, 2011, 91 (02) :117-126
[2]   RD5-mediated lack of PE_PGRS and PPE-MPTR export in BCG vaccine strains results in strong reduction of antigenic repertoire but little impact on protection [J].
Ates, Louis S. ;
Sayes, Fadel ;
Frigui, Wafa ;
Ummels, Roy ;
Damen, Merel P. M. ;
Bottai, Daria ;
Behr, Marcel A. ;
van Heijst, Jeroen W. J. ;
Bitter, Wilbert ;
Majlessi, Laleh ;
Brosch, Roland .
PLOS PATHOGENS, 2018, 14 (06)
[3]   Mutations in ppe38 block PE_PGRS secretion and increase virulence of Mycobacterium tuberculosis [J].
Ates, Louis S. ;
Dippenaar, Anzaan ;
Ummels, Roy ;
Piersma, Sander R. ;
van der Woude, Aniek D. ;
van der Kuij, Kim ;
Le Chevalier, Fabien ;
Mata-Espinosa, Dulce ;
Barrios-Payan, Jorge ;
Marquina-Castillo, Brenda ;
Guapillo, Carolina ;
Jimenez, Connie R. ;
Pain, Arnab ;
Houben, Edith N. G. ;
Warren, Robin M. ;
Brosch, Roland ;
Hernandez-Pando, Rogelio ;
Bitter, Wilbert .
NATURE MICROBIOLOGY, 2018, 3 (02) :181-188
[4]   Mapping of IS6110 insertion sites in two epidemic strains of Mycobacterium tuberculosis [J].
Beggs, ML ;
Eisenach, KD ;
Cave, MD .
JOURNAL OF CLINICAL MICROBIOLOGY, 2000, 38 (08) :2923-2928
[5]   DIAGNOSIS OF TUBERCULOSIS BY DNA AMPLIFICATION IN CLINICAL-PRACTICE EVALUATION [J].
BRISSONNOEL, A ;
AZNAR, C ;
CHUREAU, C ;
NGUYEN, S ;
PIERRE, C ;
BARTOLI, M ;
BONETE, R ;
PIALOUX, G ;
GICQUEL, B ;
GARRIGUE, G .
LANCET, 1991, 338 (8763) :364-366
[6]   Genomic analysis reveals variation between Mycobacterium tuberculosis H37Rv and the attenuated M. tuberculosis H37Ra strain [J].
Brosch, R ;
Philipp, WJ ;
Stavropoulos, E ;
Colston, MJ ;
Cole, ST ;
Gordon, SV .
INFECTION AND IMMUNITY, 1999, 67 (11) :5768-5774
[7]   Analysis of Mycobacterium africanum in the last 17 years in Aragon identifies a specific location of IS6110 in Lineage 6 [J].
Comin, Jessica ;
Luisa Monforte, Maria ;
Samper, Sofia ;
Otal, Isabel .
SCIENTIFIC REPORTS, 2021, 11 (01)
[8]   A whole-genome sequencing study of an X-family tuberculosis outbreak focus on transmission chain along 25 years [J].
Comin, Jessica ;
Cebollada, Alberto ;
Ibarz, Daniel ;
Vinuelas, Jesus ;
Asuncion Vitoria, Maria ;
Jose Iglesias, Maria ;
Samper, Sofia .
TUBERCULOSIS, 2021, 126
[9]   Investigation of a rapidly spreading tuberculosis outbreak using whole-genome sequencing [J].
Comin, Jessica ;
Chaure, Armando ;
Cebollada, Alberto ;
Ibarz, Daniel ;
Vinuelas, Jesus ;
Asuncion Vitoria, Maria ;
Jose Iglesias, Maria ;
Samper, Sofia .
INFECTION GENETICS AND EVOLUTION, 2020, 81
[10]  
DALE JW, 1995, EUR RESPIR J, V8, pS633