Two NIS1-like proteins from apple canker pathogen (Valsa mali) play distinct roles in plant recognition and pathogen virulence

Jiajun Nie, Wenjing Zhou, Yonghui Lin, Zhaoyang Liu, Zhiyuan Yin, Lili Huang

Stress Biology ›› 2022, Vol. 2 ›› Issue (1) : 7. DOI: 10.1007/s44154-021-00031-0
Original Paper

Two NIS1-like proteins from apple canker pathogen (Valsa mali) play distinct roles in plant recognition and pathogen virulence

Author information +
History +

Abstract

Conserved effectors produced by phytopathogens play critical roles in plant-microbe interactions. NIS1-like proteins represent a newly identified family of effectors distributed in multiple fungal species. However, their biological functions in a majority of pathogenic fungi remain largely elusive and require further investigation. In this study, we characterized two NIS1-like proteins VmNIS1 and VmNIS2 from Valsa mali, the causal agent of apple Valsa canker. Both of these two proteins were predicted to be secreted. Using agroinfiltration, we found that VmNIS1 induced intense cell death, whereas VmNIS2 suppressed INF1 elicitin-triggered cell death in Nicotiana benthamiana. Treatment of N. benthamiana with VmNIS1 recombinant protein produced by Escherichia coli activated a series of immune responses and enhanced plant disease resistance against Phytophthora capsici. In contrast, VmNIS2 suppressed plant immune responses and promoted P. capsici infection when transiently expressed in N. benthamiana. Both VmNIS1 and VmNIS2 were shown to be highly induced at late stage of V. mali infection. By individually knocking out of these two genes in V. mali, however, only VmNIS2 was shown to be required for pathogen virulence as well as tolerance to oxidative stress. Notably, we further showed that C-terminal extension of VmNIS1 was essential for plant recognition and VmNIS2 may escape plant detection via sequence truncation. Our data collectively indicate that VmNIS1 and VmNIS2 play distinct roles in plant recognition and pathogen virulence, which provided new insights into the function of NIS1-like proteins in plant-microbe interactions.

Keywords

Valsa mali / Effector protein / Cell death / Plant immunity / Virulence

Cite this article

Download citation ▾
Jiajun Nie, Wenjing Zhou, Yonghui Lin, Zhaoyang Liu, Zhiyuan Yin, Lili Huang. Two NIS1-like proteins from apple canker pathogen (Valsa mali) play distinct roles in plant recognition and pathogen virulence. Stress Biology, 2022, 2(1): 7 https://doi.org/10.1007/s44154-021-00031-0

References

[1]
AmsellemZ, CohenBA, GresselJ. Engineering hypervirulence in a mycoherbicidal fungus for efficient weed control. Nat Biotechnol, 2002, 20(10):1035-1039
CrossRef Google scholar
[2]
AsaiS, YoshiokaH. Nitric oxide as a partner of reactive oxygen species participates in disease resistance to necrotrophic pathogen Botrytis cinerea in Nicotiana benthamiana. Mol Plant-Microbe Interact, 2009, 22(6):619-629
CrossRef Google scholar
[3]
BollerT, FelixG. A renaissance of elicitors: perception of microbe-associated molecular patterns and danger signals by pattern-recognition receptors. Annu Rev Plant Biol, 2009, 60(1):379-406
CrossRef Google scholar
[4]
BoltonMD, Van EsseHP, VossenJH, De JongeR, StergiopoulosI, StulemeijerIJ, et al.. The novel Cladosporium fulvum lysin motif effector Ecp6 is a virulence factor with orthologues in other fungal species. Mol Microbiol, 2008, 69(1):119-136
CrossRef Google scholar
[5]
BoutrotF, ZipfelC. Function, discovery, and exploitation of plant pattern recognition receptors for broad-spectrum disease resistance. Annu Rev Phytopathol, 2017, 55(1):257-286
CrossRef Google scholar
[6]
Chang H-X, Domier LL, Radwan O, Yendrek CR, Hudson ME, Hartman GL (2016) Identification of multiple phytotoxins produced by Fusarium virguliforme including a phytotoxic effector (FvNIS1) associated with sudden death syndrome foliar symptoms. Mol Plant-Microbe Interact 29:96–108. https://doi.org/10.1094/MPMI-09-15-0219-R
[7]
ChinchillaD, ZipfelC, RobatzekS, KemmerlingB, NürnbergerT, JonesJD, et al.. A flagellin-induced complex of the receptor FLS2 and BAK1 initiates plant defence. Nature, 2007, 448(7152):497-500
CrossRef Google scholar
[8]
CuiH, TsudaK, ParkerJE. Effector-triggered immunity: from pathogen perception to robust defense. Annu Rev Plant Biol, 2015, 66(1):487-511
CrossRef Google scholar
[9]
De JongeR, Van EsseHP, KombrinkA, ShinyaT, DesakiY, BoursR, et al.. Conserved fungal LysM effector Ecp6 prevents chitin-triggered immunity in plants. Science, 2010, 329(5994):953-955
CrossRef Google scholar
[10]
DeanJ, GoodwinP, HsiangT. Induction of glutathione S-transferase genes of Nicotiana benthamiana following infection by Colletotrichum destructivum and C. orbiculare and involvement of one in resistance. J Exp Bot, 2005, 56(416):1525-1533
CrossRef Google scholar
[11]
DeslandesL, RivasS. Catch me if you can: bacterial effectors and plant targets. Trends Plant Sci, 2012, 17(11):644-655
CrossRef Google scholar
[12]
DoddsPN, RathjenJP. Plant immunity: towards an integrated view of plant–pathogen interactions. Nat Rev Genet, 2010, 11(8):539-548
CrossRef Google scholar
[13]
GijzenM, NürnbergerT. Nep1-like proteins from plant pathogens: recruitment and diversification of the NPP1 domain across taxa. Phytochemistry, 2006, 67(16):1800-1807
CrossRef Google scholar
[14]
GiraldoMC, ValentB. Filamentous plant pathogen effectors in action. Nat Rev Microbiol, 2013, 11(11):800-814
CrossRef Google scholar
[15]
HeeseA, HannDR, Gimenez-IbanezS, JonesAM, HeK, LiJ, et al.. The receptor-like kinase SERK3/BAK1 is a central regulator of innate immunity in plants. Proc Natl Acad Sci, 2007, 104(29):12217-12222
CrossRef Google scholar
[16]
HemetsbergerC, MuellerAN, MateiA, HerrbergerC, HenselG, KumlehnJ, MishraB, SharmaR, ThinesM, HückelhovenR, DoehlemannG. The fungal core effector Pep1 is conserved across smuts of dicots and monocots. New Phytol, 2015, 206(3):1116-1126
CrossRef Google scholar
[17]
IriedaH, InoueY, MoriM, YamadaK, OshikawaY, SaitohH, UemuraA, TerauchiR, KitakuraS, KosakaA, Singkaravanit-OgawaS, TakanoY. Conserved fungal effector suppresses PAMP-triggered immunity by targeting plant immune kinases. Proc Natl Acad Sci, 2019, 116(2):496-505
CrossRef Google scholar
[18]
JonesJD, DanglJL. The plant immune system. Nature, 2006, 444: 323-329
CrossRef Google scholar
[19]
KumarS, StecherG, LiM, KnyazC, TamuraK. MEGA X: molecular evolutionary genetics analysis across computing platforms. Mol Biol Evol, 2018, 35(6):1547-1549
CrossRef Google scholar
[20]
Li T, Wang Q, Feng R, Li L, Ding L, Fan G, Li W, du Y, Zhang M, Huang G, Schäfer P, Meng Y, Tyler BM, Shan W (2019) Negative regulators of plant immunity derived from cinnamyl alcohol dehydrogenases are targeted by multiple Phytophthora Avr3a-like effectors. New Phytol. https://doi.org/10.1111/nph.16139
[21]
Li Z, Yin Z, Fan Y, Xu M, Kang Z, Huang L (2015) Candidate effector proteins of the necrotrophic apple canker pathogen Valsa mali can suppress BAX-induced PCD. Front Plant Sci 6:579. https://doi.org/10.3389/fpls.2015.00579
[22]
LivakKJ, SchmittgenTD. Analysis of relative gene expression data using real-time quantitative PCR and the 2− ΔΔCT method. Methods, 2001, 25: 402-408
CrossRef Google scholar
[23]
LolleS, StevensD, CoakerG. Plant NLR-triggered immunity: from receptor activation to downstream signaling. Curr Opin Immunol, 2020, 62: 99-105
CrossRef Google scholar
[24]
MaZ, SongT, ZhuL, YeW, WangY, ShaoY, DongS, ZhangZ, DouD, ZhengX, TylerBM, WangY. A Phytophthora sojae glycoside hydrolase 12 protein is a major virulence factor during soybean infection and is recognized as a PAMP. Plant Cell, 2015, 27(7):2057-2072
CrossRef Google scholar
[25]
MaZ, ZhuL, SongT, WangY, ZhangQ, XiaY, QiuM, LinY, LiH, KongL, FangY, YeW, WangY, DongS, ZhengX, TylerBM, WangY. A paralogous decoy protects Phytophthora sojae apoplastic effector PsXEG1 from a host inhibitor. Science, 2017, 355(6326):710-714
CrossRef Google scholar
[26]
MartelA, Ruiz-BedoyaT, Breit-McNallyC, LaflammeB, DesveauxD, GuttmanDS. The ETS-ETI cycle: evolutionary processes and metapopulation dynamics driving the diversification of pathogen effectors and host immune factors. Curr Opin Plant Biol, 2021, 62: 102011
CrossRef Google scholar
[27]
McLellanH, BoevinkPC, ArmstrongMR, PritchardL, GomezS, MoralesJ, WhissonSC, BeynonJL, BirchPRJ. An RxLR effector from Phytophthora infestans prevents re-localisation of two plant NAC transcription factors from the endoplasmic reticulum to the nucleus. PLoS Pathog, 2013, 9(10):e1003670
CrossRef Google scholar
[28]
NieJ, YinZ, LiZ, WuY, HuangL. A small cysteine-rich protein from two kingdoms of microbes is recognized as a novel pathogen-associated molecular pattern. New Phytol, 2019, 222(2):995-1011
CrossRef Google scholar
[29]
NieJ, ZhouW, LiuJ, TanN, ZhouJM, HuangL. A receptor-like protein from Nicotiana benthamiana mediates VmE02 PAMP-triggered immunity. New Phytol, 2021, 229(4):2260-2272
CrossRef Google scholar
[30]
NürnbergerT, BrunnerF. Innate immunity in plants and animals: emerging parallels between the recognition of general elicitors and pathogen-associated molecular patterns. Curr Opin Plant Biol, 2002, 5(4):318-324
CrossRef Google scholar
[31]
OomeS, Van den AckervekenG. Comparative and functional analysis of the widely occurring family of Nep1-like proteins. Mol Plant-Microbe Interact, 2014, 27(10):1081-1094
CrossRef Google scholar
[32]
OttmannC, LuberackiB, KüfnerI, KochW, BrunnerF, WeyandM, et al.. A common toxin fold mediates microbial attack and plant defense. Proc Natl Acad Sci, 2009, 106(25):10359-10364
CrossRef Google scholar
[33]
ParkCH, ShirsekarG, BellizziM, ChenS, SongkumarnP, XieX, ShiX, NingY, ZhouB, SuttiviriyaP, WangM, UmemuraK, WangGL. The E3 ligase APIP10 connects the effector AvrPiz-t to the NLR receptor Piz-t in rice. PLoS Pathog, 2016, 12(3):e1005529
CrossRef Google scholar
[34]
PaulusJK, KourelisJ, van der HoornRA. Bodyguards: pathogen-derived decoys that protect virulence factors. Trends Plant Sci, 2017, 22(5):355-357
CrossRef Google scholar
[35]
Pontier D, Godiard L, Marco Y, Roby D (1994) hsr203J, a tobacco gene whose activation is rapid, highly localized and specific for incompatible plant/pathogen interactions. Plant J 5(4):507–521. https://doi.org/10.1046/j.1365-313X.1994.05040507.x
[36]
RodriguezPA, StamR, WarbroekT, BosJI. Mp10 and Mp42 from the aphid species Myzus persicae trigger plant defenses in Nicotiana benthamiana through different activities. Mol Plant-Microbe Interact, 2014, 27(1):30-39
CrossRef Google scholar
[37]
SainsburyF, LomonossoffGP. Extremely high-level and rapid transient protein production in plants without the use of viral replication. Plant Physiol, 2008, 148(3):1212-1218
CrossRef Google scholar
[38]
SanthanamP, van EsseHP, AlbertI, FainoL, NürnbergerT, ThommaBP. Evidence for functional diversification within a fungal NEP1-like protein family. Mol Plant-Microbe Interact, 2013, 26(3):278-286
CrossRef Google scholar
[39]
Takahashi Y, Berberich T, Yamashita K, Uehara Y, Miyazaki A, Kusano T (2004) Identification of tobacco HIN1 and two closely related genes as spermine-responsive genes and their differential expression during the tobacco mosaic virus-induced hypersensitive response and during leaf-and flower-senescence. Plant Mol Biol 54(4):613–622. https://doi.org/10.1023/B:PLAN.0000038276.95539.39
[40]
TogashiK. Some studies on a Japanese apple canker and its causal fungus, Valsa mali. J Coll Agric, Hokkaido Imp Univ, Sapporo, Jpn, 1925, 12: 265-324
[41]
ToruñoTY, StergiopoulosI, CoakerG. Plant-pathogen effectors: cellular probes interfering with plant defenses in spatial and temporal manners. Annu Rev Phytopathol, 2016, 54(1):419-441
CrossRef Google scholar
[42]
UhmJY, SohnHR. Control of apple Valsa canker by localized spraying with neoasozin solution, an arsenic fungicide. Plant Pathol J, 1995, 11: 9-16
[43]
WangX, WeiJ, HuangL, KangZ. Re-evaluation of pathogens causing Valsa canker on apple in China. Mycologia, 2011, 103(2):317-324
CrossRef Google scholar
[44]
WangX, ShiC-M, GleasonML, HuangL. Fungal species associated with apple Valsa canker in East Asia. Phytopathol Res, 2020, 2(1):1-14
CrossRef Google scholar
[45]
WeiJ, HuangL, GaoZ, KeX, KangZ. Laboratory evaluation methods of apple Valsa canker disease caused by Valsa ceratosperma sensu Kobayashi. Acta Phytopathol Sin, 2010, 40: 14-20
[46]
YangG, TangL, GongY, XieJ, FuY, JiangD, LiG, CollingeDB, ChenW, ChengJ. A cerato-platanin protein SsCP1 targets plant PR1 and contributes to virulence of Sclerotinia sclerotiorum. New Phytol, 2018, 217(2):739-755
CrossRef Google scholar
[47]
YasudaS, OkadaK, SaijoY. A look at plant immunity through the window of the multitasking coreceptor BAK1. Curr Opin Plant Biol, 2017, 38: 10-18
CrossRef Google scholar
[48]
Yin Z, Ke X, Huang D, Gao X, Voegele RT, Kang Z, Huang L (2013) Validation of reference genes for gene expression analysis in Valsa mali var. mali using real-time quantitative PCR. World J Microbiol Biotechnol 29(9):1563–1571. https://doi.org/10.1007/s11274-013-1320-6
[49]
YinZ, LiuH, LiZ, KeX, DouD, GaoX, SongN, DaiQ, WuY, XuJR, KangZ, HuangL. Genome sequence of Valsa canker pathogens uncovers a potential adaptation of colonization of woody bark. New Phytol, 2015, 208(4):1202-1216
CrossRef Google scholar
[50]
YoshinoK, IriedaH, SugimotoF, YoshiokaH, OkunoT, TakanoY. Cell death of Nicotiana benthamiana is induced by secreted protein NIS1 of Colletotrichum orbiculare and is suppressed by a homologue of CgDN3. Mol Plant-Microbe Interact, 2012, 25(5):625-636
CrossRef Google scholar
[51]
YuX, TangJ, WangQ, YeW, TaoK, DuanS, LuC, YangX, DongS, ZhengX, WangY. The RxLR effector Avh241 from Phytophthora sojae requires plasma membrane localization to induce plant cell death. New Phytol, 2012, 196(1):247-260
CrossRef Google scholar
[52]
ZhangM, FengH, ZhaoY, SongL, GaoC, XuX, HuangL. Valsa mali pathogenic effector VmPxE1 contributes to full virulence and interacts with the host peroxidase MdAPX1 as a potential target. Front Microbiol, 2018, 9: 821
CrossRef Google scholar
[53]
ZhangM, XieS, ZhaoY, MengX, SongL, FengH, HuangL. Hce2 domain-containing effectors contribute to the full virulence of Valsa mali in a redundant manner. Mol Plant Pathol, 2019, 20(6):843-856
CrossRef Google scholar
[54]
ZhouX, LiG, XuJ-R. Efficient approaches for generating GFP fusion and epitope-tagging constructs in filamentous fungi, 2011 In Fungal Genomics Springer 199-212
Funding
Postdoctoral Research Foundation of China(2021M690128); National Natural Science Foundation-Xinjiang Joint Foundation of China(U1903206); Open Project Program of State Key Laboratory of Crop Stress Biology for Arid Areas(CSBAA2020011); Major Scientific and Technological Projects of Shaanxi Province(2020zdzx03-03-01)

Accesses

Citations

Detail

Sections
Recommended

/