Identification of MARVELous Protein Markers for Phytophthora infestans Extracellular Vesicles

TY - JOUR

T1 - Identification of MARVELous Protein Markers for Phytophthora infestans Extracellular Vesicles

AU - Breen, Susan

AU - McLellan, Hazel

AU - Wang, Wei

AU - Wang, Shumei

AU - Welsh, Lydia

AU - Pham, Jasmine

AU - Whisson, Stephen C.

AU - Boevink, Petra C.

AU - Birch, Paul R.J.

N1 - Publisher Copyright: © 2025 The Author(s). Journal of Extracellular Vesicles published by Wiley Periodicals LLC on behalf of International Society for Extracellular Vesicles.

PY - 2025/9/23

Y1 - 2025/9/23

N2 - Extracellular vesicles (EVs) are released from cells by unconventional secretion, but little is known about the biogenesis routes, composition or cargoes of EVs from fungal or oomycete plant pathogens. We investigated the proteome of EV-associated proteins secreted by the oomycete Phytophthora infestans, cause of potato late blight disease. We found that vesicle-associated proteins, transmembrane proteins and RxLR effectors, which are delivered into host cells to suppress immunity, were enriched in the EV proteome. By contrast, the EV-independent secreted proteome was enriched in cell wall modifying enzymes and apoplastic effectors which act outside plant cells. Two proteins, each containing two tetraspanning MARVEL domains, PiMDP1 and PiMDP2, were associated with P. infestans EVs. PiMDP1 and PiMDP2 were co-buoyant with RxLR effectors in sucrose density fractions containing EVs and co-localised frequently with each other and with RxLRs at vesicles within pathogen hyphae grown in vitro and during infection. Interestingly, PiMDP2, which is up-regulated during the early biotrophic phase of infection, accumulates at the haustorial interface, a major site of effector secretion during infection. We argue that PiMDP1 and PiMDP2 are molecular markers that will facilitate studies of the biogenesis and secretion of infection-associated P. infestans EVs.

AB - Extracellular vesicles (EVs) are released from cells by unconventional secretion, but little is known about the biogenesis routes, composition or cargoes of EVs from fungal or oomycete plant pathogens. We investigated the proteome of EV-associated proteins secreted by the oomycete Phytophthora infestans, cause of potato late blight disease. We found that vesicle-associated proteins, transmembrane proteins and RxLR effectors, which are delivered into host cells to suppress immunity, were enriched in the EV proteome. By contrast, the EV-independent secreted proteome was enriched in cell wall modifying enzymes and apoplastic effectors which act outside plant cells. Two proteins, each containing two tetraspanning MARVEL domains, PiMDP1 and PiMDP2, were associated with P. infestans EVs. PiMDP1 and PiMDP2 were co-buoyant with RxLR effectors in sucrose density fractions containing EVs and co-localised frequently with each other and with RxLRs at vesicles within pathogen hyphae grown in vitro and during infection. Interestingly, PiMDP2, which is up-regulated during the early biotrophic phase of infection, accumulates at the haustorial interface, a major site of effector secretion during infection. We argue that PiMDP1 and PiMDP2 are molecular markers that will facilitate studies of the biogenesis and secretion of infection-associated P. infestans EVs.

KW - extracellular vesicles

KW - MARVEL domain

KW - pathogen effector

KW - Phytophthora infestans

KW - RxLR

UR - https://www.scopus.com/pages/publications/105017036739

U2 - 10.1002/jev2.70101

DO - 10.1002/jev2.70101

M3 - Article

C2 - 40988107

AN - SCOPUS:105017036739

SN - 2001-3078

VL - 14

JO - Journal of Extracellular Vesicles

JF - Journal of Extracellular Vesicles

IS - 9

M1 - e70101

ER -