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1.
J Clin Microbiol ; 51(4): 1305-6, 2013 Apr.
Article in English | MEDLINE | ID: mdl-23390279

ABSTRACT

The Xpert GBS real-time PCR assay for the detection of group B streptococci (GBS) in antepartum screening samples was evaluated on amniotic fluid samples collected from 139 women with premature rupture of membrane at term. When any intrapartum positive result from the Xpert GBS or culture was considered a true positive, the sensitivities of the Xpert GBS and culture were 92.3% and 84.6%, respectively. This assay could enhance exact identification of candidates for intrapartum antibiotic prophylaxis.


Subject(s)
Bacteriological Techniques/methods , Fetal Membranes, Premature Rupture , Molecular Diagnostic Techniques/methods , Pregnancy Complications, Infectious/diagnosis , Real-Time Polymerase Chain Reaction/methods , Streptococcal Infections/diagnosis , Streptococcus agalactiae/isolation & purification , Female , Humans , Pregnancy , Prospective Studies , Streptococcus agalactiae/genetics , Streptococcus agalactiae/growth & development
2.
J Clin Microbiol ; 43(6): 2567-74, 2005 Jun.
Article in English | MEDLINE | ID: mdl-15956365

ABSTRACT

Using INNO-LiPA-MYCOBACTERIA (Lipav1; Innogenetics) and the AccuProbe (Gen-Probe Inc./bioMérieux) techniques, 35 Mycobacterium avium-Mycobacterium intracellulare-Mycobacterium scrofulaceum (MAC/MAIS) complex strains were identified between January 2000 and December 2002. Thirty-four of 35 isolates were positive only for the MAIS complex probe by Lipav1 and were further analyzed by INNO-LiPA-MYCOBACTERIA version 2 (Lipav2), hsp65 PCR restriction pattern analysis (PRA), and ribosomal internal transcribed spacer (ITS), hsp65, and 16S rRNA sequences. Lipav2 identified 14 of 34 strains at the species level, including 11 isolates positive for the newly specific MAC sequevar Mac-A probe (MIN-2 probe). Ten of these 11 isolates corresponded to sequevar Mac-A, which was recently defined as Mycobacterium chimerae sp. nov. Among the last 20 of the 34 MAIS isolates, 17 (by hsp65 PRA) and 18 (by hsp65 sequence) were characterized as M. avium. Ten of the 20 were identified as Mac-U sequevar. All these 20 isolates were identified as M. intracellulare by 16S rRNA sequence except one isolate identified as Mycobacterium paraffinicum by 16S rRNA and ITS sequencing. One isolate out of 35 isolates that was positive for M. avium by AccuProbe and that was Mycobacterium genus probe positive and MAIS probe negative by Lipav1 and Lipav2 might be considered a new species. In conclusion, the new INNO-LiPA-MYCOBACTERIA allowed the identification of 40% of the previously unidentified MAIS isolates at the species level. The results of the Lipav2 assay on the MAIS isolates confirm the great heterogeneity of this group and suggest the use of hsp65 or ITS sequencing for precise identification of such isolates.


Subject(s)
Mycobacterium Infections/diagnosis , Mycobacterium avium Complex/classification , Mycobacterium scrofulaceum/classification , Nucleic Acid Hybridization/methods , Bacterial Proteins/genetics , Chaperonin 60 , Chaperonins/genetics , DNA Probes , Humans , Molecular Sequence Data , Mycobacterium Infections/microbiology , Mycobacterium avium Complex/genetics , Mycobacterium avium Complex/isolation & purification , Mycobacterium scrofulaceum/genetics , Mycobacterium scrofulaceum/isolation & purification , Polymerase Chain Reaction , RNA, Ribosomal, 16S/genetics , Reagent Kits, Diagnostic , Sensitivity and Specificity , Sequence Analysis, DNA , Species Specificity
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