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lytA-based identification methods can misidentify Streptococcus pneumoniae.
- Source :
-
Diagnostic microbiology and infectious disease [Diagn Microbiol Infect Dis] 2016 Jun; Vol. 85 (2), pp. 141-8. Date of Electronic Publication: 2016 Mar 29. - Publication Year :
- 2016
-
Abstract
- During surveillance studies we detected, among over 1500 presumptive pneumococci, 11 isolates displaying conflicting or novel results when characterized by widely accepted phenotypic (optochin susceptibility and bile solubility) and genotypic (lytA-BsaAI-RFLP and MLST) identification methods. We aimed to determine the genetic basis for the unexpected results given by lytA-BsaAI-RFLP and investigate the accuracy of the WHO recommended lytA real-time PCR assay to classify these 11 isolates. Three novel lytA-BsaAI-RFLP signatures were found (one in pneumococcus and two in S. mitis). In addition, one pneumococcus displayed the atypical lytA-BsaAI-RFLP signature characteristic of non-pneumococci and two S. pseudopneumoniae displayed the typical lytA-BsaAI-RFLP pattern characteristic of pneumococci. lytA real-time PCR misidentified these three isolates. In conclusion, identification of pneumococci by lytA real-time PCR, and other lytA-based methodologies, may lead to false results. This is of particular relevance in the increasingly frequent colonization studies relying solely on culture-independent methods.<br /> (Copyright © 2016 Elsevier Inc. All rights reserved.)
- Subjects :
- Adult
Aged
Child, Preschool
Female
Humans
Male
Middle Aged
Pneumococcal Infections microbiology
Real-Time Polymerase Chain Reaction methods
Bacterial Typing Techniques methods
Diagnostic Errors
Molecular Diagnostic Techniques methods
Pneumococcal Infections diagnosis
Streptococcus pneumoniae isolation & purification
Subjects
Details
- Language :
- English
- ISSN :
- 1879-0070
- Volume :
- 85
- Issue :
- 2
- Database :
- MEDLINE
- Journal :
- Diagnostic microbiology and infectious disease
- Publication Type :
- Academic Journal
- Accession number :
- 27107535
- Full Text :
- https://doi.org/10.1016/j.diagmicrobio.2016.03.018