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亚基因组微阵列分析揭示的σB和PrfA对单核细胞增生李斯特菌内化素及内化素样基因的差异调控

Differential regulation of Listeria monocytogenes internalin and internalin-like genes by sigmaB and PrfA as revealed by subgenomic microarray analyses.

作者信息

McGann Patrick, Raengpradub Sarita, Ivanek Renata, Wiedmann Martin, Boor Kathryn J

机构信息

Department of Food Science, Cornell University, Ithaca, New York 14853, USA.

出版信息

Foodborne Pathog Dis. 2008 Aug;5(4):417-35. doi: 10.1089/fpd.2008.0085.

Abstract

The Listeria monocytogenes genome contains more than 20 genes that encode cell surface-associated internalins. To determine the contributions of the alternative sigma factor sigma(B) and the virulence gene regulator PrfA to internalin gene expression, a subgenomic microarray was designed to contain two probes for each of 24 internalin-like genes identified in the L. monocytogenes 10403S genome. Competitive microarray hybridization was performed on RNA extracted from (i) the 10403S parent strain and an isogenic Delta sigB strain; (ii) 10403S and an isogenic Delta prfA strain; (iii) a (G155S) 10403S derivative that expresses the constitutively active PrfA (PrfA*) and the Delta prfA strain; and (iv) 10403S and an isogenic Delta sigB Delta prfA strain. Sigma(B)- and PrfA-dependent transcription of selected genes was further confirmed by quantitative reverse-transcriptase polymerase chain reaction. For the 24 internalin-like genes examined, (i) both sigma(B) and PrfA contributed to transcription of inlA and inlB, (ii) only sigma(B) contributed to transcription of inlC2, inlD, lmo0331, and lmo0610; (iii) only PrfA contributed to transcription of inlC and lmo2445; and (iv) neither sigma(B) nor PrfA contributed to transcription of the remaining 16 internalin-like genes under the conditions tested.

摘要

单核细胞增生李斯特菌的基因组包含20多个编码细胞表面相关内化素的基因。为了确定替代sigma因子sigma(B)和毒力基因调节因子PrfA对内化素基因表达的作用,设计了一个亚基因组微阵列,其中包含针对在单核细胞增生李斯特菌10403S基因组中鉴定出的24个类内化素基因中的每一个的两个探针。对从以下样本中提取的RNA进行竞争性微阵列杂交:(i) 10403S亲本菌株和同基因的Delta sigB菌株;(ii) 10403S和同基因的Delta prfA菌株;(iii) 表达组成型活性PrfA(PrfA*)的(G155S) 10403S衍生物和Delta prfA菌株;以及(iv) 10403S和同基因的Delta sigB Delta prfA菌株。通过定量逆转录酶聚合酶链反应进一步证实了所选基因的sigma(B)和PrfA依赖性转录。对于所检测的24个类内化素基因,(i) sigma(B)和PrfA都对inlA和inlB的转录有贡献;(ii) 只有sigma(B)对inlC2、inlD、lmo0331和lmo0610的转录有贡献;(iii) 只有PrfA对inlC和lmo2445的转录有贡献;以及(iv) 在测试条件下,sigma(B)和PrfA都对其余16个类内化素基因的转录没有贡献。

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