4.7 Article

Real-time PCR identification of Listeria monocytogenes serotype 4c using primers for novel target genes obtained by comparative genomic analysis

期刊

LWT-FOOD SCIENCE AND TECHNOLOGY
卷 138, 期 -, 页码 -

出版社

ELSEVIER
DOI: 10.1016/j.lwt.2020.110774

关键词

Listeria monocytogenes serotype 4c; Comparative genomics; Novel molecular targets; Real-time PCR

资金

  1. National Key R&D Program of China [2019YFC1606300]
  2. Science and Technology Projects of Guangzhou [201707020036]
  3. GDAS' Project of Science and Technology Development [2019GDASYL-0201001]

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The study identified novel target genes using comparative genomics for the specific detection of Listeria monocytogenes serotype 4c, an important serotype in aquatic products. A real-time PCR assay based on these target genes showed robust specificity and sensitivity for detecting serotype 4c, even in the presence of other L. monocytogenes serotypes and non-L. monocytogenes strains. The assay successfully detected serotype 4c in artificially contaminated grass carp without enrichment, demonstrating its potential for accurate and sensitive detection in food products.
Detection of the foodborne pathogen Listeria monocytogenes serotype 4c, one of the predominant serotypes in aquatic products, is difficult and time-consuming. Our objective was to identify novel target genes for real-time PCR detection of L. monocytogenes serotype 4c using comparative genomics to facilitate its specific identification in food products. A total of 160 Listeria genome sequences, including those of 12 L. monocytogenes serotypes and 14 other Listeria species, were employed to identify serotype 4c-specific targets. Two serotype 4c-specific genes (SLCC2376_00062 and SLCC2376_00822) were obtained. Using primers for SLCC2376_00822, a real-time PCR assay for the detection of serotype 4c was developed. The specificty of this assay was robustly verified by other serotypes of L. monocytogenes and non-L. monocytogenes strains. In addition, this real-time PCR method could accurately detect serotype 4c even when mixed with different concentrations of serotypes 1/2a and 1/2b. Furthermore, the assay could successfully detect 1.4 x 10(9) -1.4 x 10(3) CFU/g of L. monocytogenes serotype 4c in artificially contaminated grass carp without enrichment. These results demonstrate that the assay, which has high accuracy and sensitivity, comprises a promising approach for the detection and identification of L. monocytogenes serotype 4c strains in foods.

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