TY - JOUR
T1 - SNP-IT tool for identifying subspecies and associated lineages of Mycobacterium tuberculosis complex
AU - Lipworth, Samuel
AU - Jajou, Rana
AU - De Neeling, Albert
AU - Bradley, Phelim
AU - Van Der Hoek, Wim
AU - Maphalala, Gugu
AU - Bonnet, Maryline
AU - Sanchez-Padilla, Elizabeth
AU - Diel, Roland
AU - Niemann, Stefan
AU - Iqbal, Zamin
AU - Smith, Grace
AU - Peto, Tim
AU - Crook, Derrick
AU - Walker, Timothy
AU - Van Soolingen, Dick
N1 - Publisher Copyright:
© 2019, Centers for Disease Control and Prevention (CDC). All rights reserved.
PY - 2019/3
Y1 - 2019/3
N2 - The clinical phenotype of zoonotic tuberculosis and its contribution to the global burden of disease are poorly understood and probably underestimated. This shortcoming is partly because of the inability of currently available laboratory and in silico tools to accurately identify all subspecies of the Mycobacterium tuberculosis complex (MTBC). We present SNPs to Identify TB (SNP-IT), a single-nucleotide polymorphism-based tool to identify all members of MTBC, including animal clades. By applying SNP-IT to a collection of clinical genomes from a UK reference laboratory, we detected an unexpectedly high number of M. orygis isolates. M. orygis is seen at a similar rate to M. bovis, yet M. orygis cases have not been previously described in the United Kingdom. From an international perspective, it is possible that M. orygis is an underestimated zoonosis. Accurate identification will enable study of the clinical phenotype, host range, and transmission mechanisms of all subspecies of MTBCin greater detail.
AB - The clinical phenotype of zoonotic tuberculosis and its contribution to the global burden of disease are poorly understood and probably underestimated. This shortcoming is partly because of the inability of currently available laboratory and in silico tools to accurately identify all subspecies of the Mycobacterium tuberculosis complex (MTBC). We present SNPs to Identify TB (SNP-IT), a single-nucleotide polymorphism-based tool to identify all members of MTBC, including animal clades. By applying SNP-IT to a collection of clinical genomes from a UK reference laboratory, we detected an unexpectedly high number of M. orygis isolates. M. orygis is seen at a similar rate to M. bovis, yet M. orygis cases have not been previously described in the United Kingdom. From an international perspective, it is possible that M. orygis is an underestimated zoonosis. Accurate identification will enable study of the clinical phenotype, host range, and transmission mechanisms of all subspecies of MTBCin greater detail.
UR - http://www.scopus.com/inward/record.url?scp=85061960303&partnerID=8YFLogxK
U2 - 10.3201/eid2503.180894
DO - 10.3201/eid2503.180894
M3 - Article
C2 - 30789126
AN - SCOPUS:85061960303
SN - 1080-6040
VL - 25
SP - 482
EP - 488
JO - Emerging Infectious Diseases
JF - Emerging Infectious Diseases
IS - 3
ER -