4.8 Article

Cytotoxic function of xylanase VdXyn4 in the plant vascular wilt pathogen Verticillium dahliae

期刊

PLANT PHYSIOLOGY
卷 187, 期 1, 页码 409-429

出版社

OXFORD UNIV PRESS INC
DOI: 10.1093/plphys/kiab274

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资金

  1. National Key Research and Development Program of China [2018YFE0112500, 2017YFD0201900]
  2. Elite Youth Program CAAS
  3. National Natural Science Foundation of China [31972228, 31970142, 31870138, 31772245, 31671986]
  4. Agricultural Science and Technology Innovation Program grant
  5. Fundamental Research Funds for Central Non-profit Scientific Institution [Y2021XK22, Y2018PT70]

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The V. dahliae genome encodes a family of six xylanases, with VdXyn4 being the only enzyme that degrades the plant cell wall and contributes to the virulence of the pathogen. VdXyn4 displays cytotoxic activity and induces necrosis in host plants during late infection stages, playing a crucial intracellular role. This cytotoxic activity is likely conserved in other enzyme families in plant vascular pathogens, suggesting its importance for pathogen colonization.
Phytopathogen xylanases play critical roles in pathogenesis, likely due to their ability to degrade plant structural barriers and manipulate host immunity. As an invader of plant xylem vessels, the fungus Verticillium dahliae is thought to deploy complex cell wall degrading enzymes. Comparative genomics analyses revealed that the V. dahliae genome encodes a family of six xylanases, each possessing a glycosyl hydrolase 11 domain, but the functions of these enzymes are undetermined. Characterizing gene deletion mutants revealed that only V. dahliae xylanase 4 (VdXyn4) degraded the plant cell wall and contributed to the virulence of V. dahliae. VdXyn4 displayed cytotoxic activity and induced a necrosis phenotype during the late stages of infection, leading to vein and petiole collapse that depended on the enzyme simultaneously localizing to nuclei and chloroplasts. The internalization of VdXyn4 was in conjunction with that of the plasma membrane complexLeucine-rich repeat (LRR)-receptor-like kinase suppressor of BIR1-1 (SOBIR1)/LRR-RLK BRI1-associated kinase-1 (BAK1), but we could not rule out the possibility that VdXyn4 may also act as an apoplastic effector. Immune signaling (in the SA-JA pathways) induced by VdXyn4 relative to that induced by known immunity effectors was substantially delayed. While cytotoxic activity could be partially suppressed by known effectors, they failed to impede necrosis in Nicotiana benthamiana. Thus, unlike typical effectors, cytotoxicity of VdXyn4 plays a crucial intracellular role at the late stages of V. dahliae infection and colonization, especially following pathogen entry into the xylem; this cytotoxic activity is likely conserved in the corresponding enzyme families in plant vascular pathogens.

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