HexR Transcription Factor Contributes to Pseudomonas cannabina pv. alisalensis Virulence by Coordinating Type Three Secretion System Genes

Author:

Sakata Nanami1ORCID,Fujikawa Takashi2ORCID,Uke Ayaka3,Ishiga Takako4,Ichinose Yuki5,Ishiga Yasuhiro1ORCID

Affiliation:

1. Faculty of Life and Environmental Sciences, University of Tsukuba, 1-1-1 Tennodai, Tsukuba 305-8572, Ibaraki, Japan

2. Institute of Plant Protection, National Agriculture and Food Research Organization (NARO), Tsukuba 305-8666, Ibaraki, Japan

3. Biological Resources and Post-Harvest Division, Japan International Research Center for Agricultural Sciences (JIRCAS), Tsukuba 305-8686, Ibaraki, Japan

4. Tsukuba-Plant Innovation Research Center (T-PIRC), University of Tsukuba, Tsukuba 305-8572, Ibaraki, Japan

5. Graduate School of Environmental, Life, Natural Science and Technology, Okayama University, Okayama 700-8530, Okayama, Japan

Abstract

Pseudomonas cannabina pv. alisalensis (Pcal) causes bacterial blight on cabbage. We previously conducted a screening for reduced virulence using Tn5 transposon mutants and identified one of the transcriptional factors, HexR, as a potential Pcal virulence factor. However, the role of HexR in plant pathogenic Pseudomonas virulence has not been investigated well. Here, we demonstrated that the Pcal hexR mutant showed reduced disease symptoms and bacterial populations on cabbage, indicating that HexR contributes to Pcal virulence. We used RNA-seq analysis to characterize the genes regulated by HexR. We found that several type three secretion system (T3SS)-related genes had lower expression of the Pcal hexR mutant. Five genes were related to T3SS machinery, two genes were related to type three helper proteins, and three genes encoded type three effectors (T3Es). We also confirmed that T3SS-related genes, including hrpL, avrPto, hopM1, and avrE1, were also down-regulated in the Pcal hexR mutant both in culture and in vivo by using RT-qPCR. T3SS functions to suppress plant defense in host plants and induce hypersensitive response (HR) cell death in non-host plants. Therefore, we investigated the expression profiles of cabbage defense-related genes, including PR1 and PR5, and found that the expressions of these genes were greater in the Pcal hexR mutant. We also demonstrated that the hexR mutant did not induce HR cell death in non-host plants, indicating that HexR contributes in causing HR in nonhost plants. Together, these results indicate that the mutation in hexR leads to a reduction in the T3SS-related gene expression and thus an impairment in plant defense suppression, reducing Pcal virulence.

Funder

Japan Science and Technology Agency

Japan Society for the Promotion of Science

Publisher

MDPI AG

Subject

Virology,Microbiology (medical),Microbiology

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