INVESTIGADORES
IMPERIALE Belen Rocio
artículos
Título:
Genetic diversity of Mycobacterium avium complex strains isolated in Argentina by MIRU-VNTR
Autor/es:
B R IMPERIALE; R D MOYANO; A B DI GIULIO; M A ROMERO; M F ALVARADO PINEDO; M P SANTANGELO; G TRAVERIA; N S MORCILLO; M I ROMANO
Revista:
EPIDEMIOLOGY AND INFECTION.
Editorial:
CAMBRIDGE UNIV PRESS
Referencias:
Lugar: Cambridge; Año: 2017
ISSN:
0950-2688
Resumen:
Mycobacterium avium sp. avium (MAA), M. avium sp. hominissuis (MAH), and M. avium sp.paratuberculosis (MAP) are the main members of the M. avium complex (MAC) causing diseasesin several hosts. The aim of this study was to describe the genetic diversity of MAC isolated fromdifferent hosts. Twenty-six MAH and 61 MAP isolates were recovered from humans and cattle,respectively. GenoType CM® and IS1311-PCR were used to identify Mycobacterium species. TheIS901-PCR was used to differentiate between MAH and MAA, while IS900-PCR was used toidentify MAP. Genotyping was performed using a mycobacterial interspersed repetitive-unitvariable-number tandem-repeat (MIRU-VNTR) scheme (loci: 292, X3, 25, 47, 3, 7, 10, 32) andpatterns (INMV) were assigned according to the MAC-INMV database (http://mac-inmv.tours.inra.fr/). Twenty-two (22/26, 84·6%) MAH isolates were genotyped and 16 were grouped into thefollowing, INMV 92, INMV 121, INMV 97, INMV 103, INMV 50, and INMV 40. The loci X3and 25 showed the largest diversity (D: 0·5844), and the global discriminatory index (Hunter andGaston discriminatory index, HGDI) was 0·9300. MAP (100%) isolates were grouped intoINMV 1, INMV 2, INMV 11, INMV 8, and INMV 5. The HGDI was 0·6984 and loci 292 and7 had the largest D (0·6980 and 0·5050). MAH presented a higher D when compared with MAP.The MIRU-VNTR was a useful tool to describe the genetic diversity of both MAH and MAP aswell as to identify six new MAH patterns that were conveniently reported to the MAC-INMVdatabase. It was also demonstrated that, in the geographical region studied, human MAC caseswere produced by MAH as there was no MAA found among the human clinical samples.