Affiliation:
1. State Key Laboratory for Infectious Disease Prevention and Control, National Institute for Communicable Disease Control and Prevention, Chinese Center for Disease Control and Prevention, Beijing, PR China
Abstract
Accurate identification of
Nocardia
species remains a challenge due to the complexities of taxonomy and insufficient discriminatory power of traditional techniques. We report the development of a molecular technique that utilizes real-time PCR-based high-resolution melting (HRM) analysis for differentiation of the most common
Nocardia
species. Based on a novel fusA-tuf intergenic region sequence,
Nocardia farcinica
,
Nocardia cyriacigeorgica
and
Nocardia beijingensis
were clearly distinguished from one another by HRM analysis. The limit of detection of the HRM assay for purified
Nocardia
spp. DNA was at least 10 fg. No false positives were observed for specificity testing of 20 non-target clinical samples. In comparison to established matrix-assisted laser desorption/ionization-time of flight MS, the HRM assay improved the identification of
N. beijingensis
. Additionally, all the products of PCR were verified by direct sequencing. In conclusion, the developed molecular assay allows simultaneous detection and differentiation of
N. farcinica
,
N. cyriacigeorgica
and
N. beijingensis
with high sensitivity and specificity.
Funder
National Key R&D Program of China
the China Special Grant for the Prevention and Control of Infectious Diseases
Subject
Microbiology (medical),General Medicine,Microbiology
Cited by
2 articles.
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