Development of a Multiplex Real-Time PCR Assay for Mycobacterium bovis BCG and Validation in a Clinical Laboratory.
Adolescent
Animals
Child
Child, Preschool
Female
Humans
Limit of Detection
Male
Mice
Mice, Inbred C57BL
Mycobacterium Infections, Nontuberculous
/ diagnosis
Mycobacterium bovis
/ genetics
Polymorphism, Single Nucleotide
/ genetics
Real-Time Polymerase Chain Reaction
/ methods
Tuberculosis
/ prevention & control
Vaccines, Attenuated
/ adverse effects
Young Adult
BCG disease
Mycobacterium bovis BCG
Mycobacterium tuberculosis
disseminated BCG
real-time PCR identification
Journal
Microbiology spectrum
ISSN: 2165-0497
Titre abrégé: Microbiol Spectr
Pays: United States
ID NLM: 101634614
Informations de publication
Date de publication:
31 10 2021
31 10 2021
Historique:
pubmed:
9
9
2021
medline:
2
2
2022
entrez:
8
9
2021
Statut:
ppublish
Résumé
Mycobacterium bovis bacillus Calmette-Guérin (BCG) is a live attenuated vaccine which can result in local or disseminated infection, most commonly in immunocompromised individuals. Differentiation of BCG from other members of the Mycobacterium tuberculosis complex (MTBC) is required to diagnose BCG disease, which requires specific management. Current methods for BCG diagnosis are based on mycobacterial culture and conventional PCR; the former is time-consuming and the latter often unavailable. Further, there are reports that certain BCG strains may be associated with a higher rate of adverse events. This study describes the development of a two-step multiplex real-time PCR assay which uses single nucleotide polymorphisms to detect BCG and identify early or late BCG strains. The assay has a limit of detection of 1 pg BCG boiled lysate DNA and was shown to detect BCG in both pure cultures and experimentally infected tissue. Its performance was assessed on 19 suspected BCG clinical isolates at Christian Medical College in Vellore, India, taken from January 2018 to August 2020. Of these 19 isolates, 10 were identified as BCG (6 early and 4 late strains), and 9 were identified as other MTBC members. Taken together, the results demonstrate the ability of this assay to identify and characterize BCG disease from cultures and infected tissue. The capacity to identify BCG may improve patient management, and the ability to discriminate between BCG strains may enable BCG vaccine pharmacovigilance.
Identifiants
pubmed: 34494864
doi: 10.1128/Spectrum.01098-21
pmc: PMC8557883
doi:
Substances chimiques
Vaccines, Attenuated
0
Types de publication
Journal Article
Research Support, Non-U.S. Gov't
Validation Study
Langues
eng
Sous-ensembles de citation
IM
Pagination
e0109821Subventions
Organisme : CIHR
ID : FDN148362
Pays : Canada
Références
J Allergy Clin Immunol. 2014 Apr;133(4):1134-41
pubmed: 24679470
Emerg Infect Dis. 2007 May;13(5):799-801
pubmed: 18044052
J Bacteriol. 2000 Jun;182(12):3394-9
pubmed: 10852869
J Clin Microbiol. 2008 Jul;46(7):2241-6
pubmed: 18508937
Jundishapur J Microbiol. 2015 Nov 21;8(11):e25663
pubmed: 26862381
Medicine (Baltimore). 2017 Dec;96(52):e9035
pubmed: 29384896
J Infect. 2012 Jun;64(6):543-54
pubmed: 22430715
Ann Acad Med Singap. 2015 Aug;44(8):297-301
pubmed: 26477962
J Clin Microbiol. 1991 Nov;29(11):2578-86
pubmed: 1685494
J Infect Dis. 1995 Aug;172(2):574-6
pubmed: 7622909
Int J Infect Dis. 2009 Nov;13(6):e420-3
pubmed: 19403320
Bull World Health Organ. 2009 Jul;87(7):505-11
pubmed: 19649364
Sci Rep. 2015 Oct 21;5:15443
pubmed: 26487098
Am J Clin Pathol. 2010 Jan;133(1):102-6
pubmed: 20023264
BMC Res Notes. 2013 Oct 29;6:434
pubmed: 24168785
Infect Immun. 2009 May;77(5):2230-8
pubmed: 19289514
Int J Infect Dis. 2020 Aug;97:117-125
pubmed: 32497805
PLoS One. 2011;6(8):e23481
pubmed: 21858140
BMJ Glob Health. 2020 Sep;5(9):
pubmed: 32978212
J Clin Microbiol. 1997 Mar;35(3):566-9
pubmed: 9041390