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HrpL Regulon of Bacterial Pathogen of Woody Host Pseudomonas savastanoi pv. savastanoi NCPPB 3335

机译:木质宿主Pseudomonas Savastanoi PV的细菌病原体HRPL稳态。 Savastanoi NCPPB 3335.

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摘要

The Pseudomonas savastanoi species comprises a group of phytopathogenic bacteria that cause symptoms of disease in woody hosts. This is mediated by the rapid activation of a pool of virulence factors that suppress host defences and hijack the host’s metabolism to the pathogen’s benefit. The hrpL gene encodes an essential transcriptional regulator of virulence functions, including the type III secretion system (T3SS), in pathogenic bacteria. Here, we analyzed the contribution of HrpL to the virulence of four pathovars (pv.) of P. savastanoi isolated from different woody hosts (oleander, ash, broom, and dipladenia) and characterized the HrpL regulon of P. savastanoi pv. savastanoi NCPPB 3335 using two approaches: whole transcriptome sequencing (RNA-seq) and the bioinformatic prediction of candidate genes containing an hrp-box. Pathogenicity tests carried out for the P. savastanoi pvs. showed that HrpL was essential for symptom development in both non-host and host plants. The RNA-seq analysis of the HrpL regulon in P. savastanoi revealed a total of 53 deregulated genes, 49 of which were downregulated in the ΔhrpL mutant. Bioinformatic prediction resulted in the identification of 50 putative genes containing an hrp-box, 16 of which were shared with genes previously identified by RNA-seq. Although most of the genes regulated by HrpL belonged to the T3SS, we also identified some genes regulated by HrpL that could encode potential virulence factors in P. savastanoi.
机译:假单胞菌萨萨瓦斯诺物种包括一组植物致病细菌,导致木质宿主中疾病的症状。这是通过抑制宿主因子池的快速激活来介导,抑制宿主防御并劫持宿主对病原体的代谢。 HRPL基因编码毒力功能的基本转录调节剂,包括在病原细菌中的III型分泌系统(T3SS)。在这里,我们分析了HRPL与不同木质主机(夹竹桃,灰,扫帚和戴卓越症)分离的四种毒素(PV。)的毒力的贡献.P.Savastanoi PV的HRPL稳态。 Savastanoi NCPPB 3335使用两种方法:整个转录组测序(RNA-SEQ)和含有HRP盒的候选基因的生物信息预测。对P. Savastanoi PVS进行的致病性测试。表明,HRPL对于非宿主和宿主植物的症状发展至关重要。 P. Savastanoi中HRPL调节件的RNA-SEQ分析显示,在ΔHRPL突变体中,共有53个张解化基因,其中49个中可解决。生物信息化预测导致鉴定含有HRP盒的50个诱导基因,其中16个与先前通过RNA-SEQ鉴定的基因共享。尽管HRPL受到的大多数基因属于T3S,但我们还确定了由HRPL调节的一些基因,其可以编码P. Savastanoi中的潜在毒力因子。

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