Moreno Luisa Zanolli, Paixão Renata, de Gobbi Debora Dirani Sena, Raimundo Daniele Cristine, Porfida Ferreira Thais Sebastiana, Micke Moreno Andrea, Hofer Ernesto, dos Reis Cristhiane Moura Falavina, Matté Glavur Rogério, Matté Maria Helena
Laboratório Prática de Saúde Pública, Faculdade de Saúde Pública, Universidade de São Paulo, Avenida Doutor Arnaldo, No. 715, 01246 904 São Paulo, SP, Brazil ; Laboratório de Sanidade Suína e Virologia, Faculdade de Medicina Veterinária e Zootecnia, Universidade de São Paulo, Avenida Professor Doutor Orlando Marques de Paiva, No. 87, Cidade Universitária, 05508 270 São Paulo, SP, Brazil.
Laboratório de Sanidade Suína e Virologia, Faculdade de Medicina Veterinária e Zootecnia, Universidade de São Paulo, Avenida Professor Doutor Orlando Marques de Paiva, No. 87, Cidade Universitária, 05508 270 São Paulo, SP, Brazil.
Biomed Res Int. 2014;2014:742032. doi: 10.1155/2014/742032. Epub 2014 May 28.
In the last decade, atypical Listeria monocytogenes and L. innocua strains have been detected in food and the environment. Because of mutations in the major virulence genes, these strains have different virulence intensities in eukaryotic cells. In this study, we performed phenotypic and genotypic characterization of atypical L. monocytogenes and L. innocua isolates obtained from swine slaughterhouses and meat markets. Forty strains were studied, including isolates of L. monocytogenes and L. innocua with low-hemolytic activity. The isolates were characterized using conventional phenotypic Listeria identification tests and by the detection and analysis of L. monocytogenes-specific genes. Analysis of 16S rRNA was used for the molecular identification of the Listeria species. The L. monocytogenes isolates were positive for all of the virulence genes studied. The atypical L. innocua strains were positive for hly, plcA, and inlC. Mutations in the InlC, InlB, InlA, PI-PLC, PC-PLC, and PrfA proteins were detected in the atypical isolates. Further in vitro and transcriptomic studies are being developed to confirm the role of these mutations in Listeria virulence.
在过去十年中,已在食品和环境中检测到非典型单核细胞增生李斯特菌和无害李斯特菌菌株。由于主要毒力基因发生突变,这些菌株在真核细胞中的毒力强度不同。在本研究中,我们对从生猪屠宰场和肉类市场获得的非典型单核细胞增生李斯特菌和无害李斯特菌分离株进行了表型和基因型特征分析。共研究了40株菌株,包括低溶血活性的单核细胞增生李斯特菌和无害李斯特菌分离株。使用传统的李斯特菌表型鉴定试验以及通过检测和分析单核细胞增生李斯特菌特异性基因对分离株进行特征分析。16S rRNA分析用于李斯特菌属的分子鉴定。所研究的所有毒力基因在单核细胞增生李斯特菌分离株中均呈阳性。非典型无害李斯特菌菌株的hly、plcA和inlC呈阳性。在非典型分离株中检测到InlC、InlB、InlA、PI-PLC、PC-PLC和PrfA蛋白的突变。正在开展进一步的体外和转录组学研究,以证实这些突变在李斯特菌毒力中的作用。