N-glycosylation shields Phytophthora sojae apoplastic effector PsXEG1 from a specific host aspartic protease
Hosts and pathogens are engaged in a continuous evolutionary struggle for physiological dominance. A major site of this struggle is the apoplast. In Phytophthora sojae–soybean interactions, PsXEG1, a pathogen-secreted apoplastic endoglucanase, is a key focal point of this struggle, and the subject o...
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Published in | Proceedings of the National Academy of Sciences - PNAS Vol. 117; no. 44; pp. 27685 - 27693 |
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Main Authors | , , , , , , , , , , , , , , , , , |
Format | Journal Article |
Language | English |
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United States
National Academy of Sciences
03.11.2020
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Abstract | Hosts and pathogens are engaged in a continuous evolutionary struggle for physiological dominance. A major site of this struggle is the apoplast. In Phytophthora sojae–soybean interactions, PsXEG1, a pathogen-secreted apoplastic endoglucanase, is a key focal point of this struggle, and the subject of two layers of host defense and pathogen counterdefense. Here, we show that N-glycosylation of PsXEG1 represents an additional layer of this coevolutionary struggle, protecting PsXEG1 against a host apoplastic aspartic protease, GmAP5, that specifically targets PsXEG1. This posttranslational modification also attenuated binding by the previously described host inhibitor, GmGIP1. N-glycosylation of PsXEG1 at N174 and N190 inhibited binding and degradation by GmAP5 and was essential for PsXEG1’s full virulence contribution, except in GmAP5-silenced soybeans. Silencing of GmAP5 reduced soybean resistance against WT P. sojae but not against PsXEG1 deletion strains of P. sojae. The crucial role of N-glycosylation within the three layers of defense and counterdefense centered on PsXEG1 highlight the critical importance of this conserved apoplastic effector and its posttranslationalmodification in Phytophthora-host coevolutionary conflict. |
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AbstractList | Hosts and pathogens are engaged in a continuous evolutionary struggle for physiological dominance. A major site of this struggle is the apoplast. In Phytophthora sojae–soybean interactions, PsXEG1, a pathogen-secreted apoplastic endoglucanase, is a key focal point of this struggle, and the subject of two layers of host defense and pathogen counterdefense. Here, we show that N-glycosylation of PsXEG1 represents an additional layer of this coevolutionary struggle, protecting PsXEG1 against a host apoplastic aspartic protease, GmAP5, that specifically targets PsXEG1. This posttranslational modification also attenuated binding by the previously described host inhibitor, GmGIP1. N-glycosylation of PsXEG1 at N174 and N190 inhibited binding and degradation by GmAP5 and was essential for PsXEG1's full virulence contribution, except in GmAP5-silenced soybeans. Silencing of GmAP5 reduced soybean resistance against WT P. sojae but not against PsXEG1 deletion strains of P. sojae. The crucial role of N-glycosylation within the three layers of defense and counterdefense centered on PsXEG1 highlight the critical importance of this conserved apoplastic effector and its posttranslational modification in Phytophthora-host coevolutionary conflict. Hosts and pathogens are engaged in a continuous evolutionary struggle for physiological dominance. A major site of this struggle is the apoplast. In -soybean interactions, PsXEG1, a pathogen-secreted apoplastic endoglucanase, is a key focal point of this struggle, and the subject of two layers of host defense and pathogen counterdefense. Here, we show that N-glycosylation of PsXEG1 represents an additional layer of this coevolutionary struggle, protecting PsXEG1 against a host apoplastic aspartic protease, GmAP5, that specifically targets PsXEG1. This posttranslational modification also attenuated binding by the previously described host inhibitor, GmGIP1. N-glycosylation of PsXEG1 at N174 and N190 inhibited binding and degradation by GmAP5 and was essential for 's full virulence contribution, except in GmAP5-silenced soybeans. Silencing of GmAP5 reduced soybean resistance against WT but not against deletion strains of The crucial role of N-glycosylation within the three layers of defense and counterdefense centered on PsXEG1 highlight the critical importance of this conserved apoplastic effector and its posttranslational modification in -host coevolutionary conflict. Hosts and pathogens are engaged in a continuous evolutionary struggle for physiological dominance. A major site of this struggle is the apoplast. In Phytophthora sojae-soybean interactions, PsXEG1, a pathogen-secreted apoplastic endoglucanase, is a key focal point of this struggle, and the subject of two layers of host defense and pathogen counterdefense. Here, we show that N-glycosylation of PsXEG1 represents an additional layer of this coevolutionary struggle, protecting PsXEG1 against a host apoplastic aspartic protease, GmAP5, that specifically targets PsXEG1. This posttranslational modification also attenuated binding by the previously described host inhibitor, GmGIP1. N-glycosylation of PsXEG1 at N174 and N190 inhibited binding and degradation by GmAP5 and was essential for PsXEG1's full virulence contribution, except in GmAP5-silenced soybeans. Silencing of GmAP5 reduced soybean resistance against WT P. sojae but not against PsXEG1 deletion strains of P. sojae. The crucial role of N-glycosylation within the three layers of defense and counterdefense centered on PsXEG1 highlight the critical importance of this conserved apoplastic effector and its posttranslational modification in Phytophthora-host coevolutionary conflict.Hosts and pathogens are engaged in a continuous evolutionary struggle for physiological dominance. A major site of this struggle is the apoplast. In Phytophthora sojae-soybean interactions, PsXEG1, a pathogen-secreted apoplastic endoglucanase, is a key focal point of this struggle, and the subject of two layers of host defense and pathogen counterdefense. Here, we show that N-glycosylation of PsXEG1 represents an additional layer of this coevolutionary struggle, protecting PsXEG1 against a host apoplastic aspartic protease, GmAP5, that specifically targets PsXEG1. This posttranslational modification also attenuated binding by the previously described host inhibitor, GmGIP1. N-glycosylation of PsXEG1 at N174 and N190 inhibited binding and degradation by GmAP5 and was essential for PsXEG1's full virulence contribution, except in GmAP5-silenced soybeans. Silencing of GmAP5 reduced soybean resistance against WT P. sojae but not against PsXEG1 deletion strains of P. sojae. The crucial role of N-glycosylation within the three layers of defense and counterdefense centered on PsXEG1 highlight the critical importance of this conserved apoplastic effector and its posttranslational modification in Phytophthora-host coevolutionary conflict. The apoplastic space is the initial battlefield in plant–microbe interactions. However, the molecular mechanisms underlying how apoplastic immunity controls pathogen invasion is still largely unknown. Here, we show that soybean secretes an apoplastic aspartic protease, GmAP5, that binds to and degrades PsXEG1 to block its contribution to virulence. Phytophthora sojae , however, employs N-glycosylation as a shield to protect PsXEG1 from degradation by GmAP5. N-glycosylation of PsXEG1 also attenuates the binding by the inhibitor GmGIP1. Our result uncovers an additional layer of defense and counterdefense centered on PsXEG1, highlighting an example in which N - glycosylation of a pathogen virulence factor tips the balance of an arms race in host–pathogen conflicts. Hosts and pathogens are engaged in a continuous evolutionary struggle for physiological dominance. A major site of this struggle is the apoplast. In Phytophthora sojae –soybean interactions, PsXEG1, a pathogen-secreted apoplastic endoglucanase, is a key focal point of this struggle, and the subject of two layers of host defense and pathogen counterdefense. Here, we show that N-glycosylation of PsXEG1 represents an additional layer of this coevolutionary struggle, protecting PsXEG1 against a host apoplastic aspartic protease, GmAP5, that specifically targets PsXEG1. This posttranslational modification also attenuated binding by the previously described host inhibitor, GmGIP1. N-glycosylation of PsXEG1 at N174 and N190 inhibited binding and degradation by GmAP5 and was essential for PsXEG1 ’s full virulence contribution, except in GmAP5-silenced soybeans. Silencing of GmAP5 reduced soybean resistance against WT P. sojae but not against PsXEG1 deletion strains of P. sojae. The crucial role of N-glycosylation within the three layers of defense and counterdefense centered on PsXEG1 highlight the critical importance of this conserved apoplastic effector and its posttranslational modification in Phytophthora -host coevolutionary conflict. Hosts and pathogens are engaged in a continuous evolutionary struggle for physiological dominance. A major site of this struggle is the apoplast. In Phytophthora sojae–soybean interactions, PsXEG1, a pathogen-secreted apoplastic endoglucanase, is a key focal point of this struggle, and the subject of two layers of host defense and pathogen counterdefense. Here, we show that N-glycosylation of PsXEG1 represents an additional layer of this coevolutionary struggle, protecting PsXEG1 against a host apoplastic aspartic protease, GmAP5, that specifically targets PsXEG1. This posttranslational modification also attenuated binding by the previously described host inhibitor, GmGIP1. N-glycosylation of PsXEG1 at N174 and N190 inhibited binding and degradation by GmAP5 and was essential for PsXEG1’s full virulence contribution, except in GmAP5-silenced soybeans. Silencing of GmAP5 reduced soybean resistance against WT P. sojae but not against PsXEG1 deletion strains of P. sojae. The crucial role of N-glycosylation within the three layers of defense and counterdefense centered on PsXEG1 highlight the critical importance of this conserved apoplastic effector and its posttranslationalmodification in Phytophthora-host coevolutionary conflict. |
Author | Xiao, Junhua Zhang, Qi Lin, Yachun Zhang, Baiyu Tyler, Brett M. Wang, Yan Wang, Yiming Dong, Suomeng Qiu, Min Ma, Zhenchuan Ye, Wenwu Sun, Liang Shu, Haidong Xia, Yeqiang Guo, Baodian Wang, Yuanchao Jiang, Haibin Xuan, Mingrun |
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Keywords | P. sojae immunity apoplast N-glycosylation aspartic protease |
Language | English |
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Notes | ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 14 content type line 23 1Present address: No.1 Weigang, Department of Plant Pathology, Nanjing Agricultural University, 210095 Nanjing, China. Edited by Sheng Yang He, Duke University, Durham, NC, and approved September 17, 2020 (received for review June 12, 2020) Author contributions: Y.X., Z.M., and Yuanchao Wang designed research; Y.X., Z.M., M.Q., B.G., Q.Z., H.J., B.Z., Y.L., M.X., L.S., H.S., J.X., W.Y., S.D., B.M.T., and Yuanchao Wang performed research; Y.X., Z.M., M.Q., B.G., Q.Z., H.J., H.S., W.Y., Yan Wang, Yiming Wang, B.M.T., and Yuanchao Wang analyzed data; and Y.X., Z.M., M.Q., Yan Wang, Yiming Wang, S.D., B.M.T., and Yuanchao Wang wrote the paper. |
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Snippet | Hosts and pathogens are engaged in a continuous evolutionary struggle for physiological dominance. A major site of this struggle is the apoplast. In... The apoplastic space is the initial battlefield in plant–microbe interactions. However, the molecular mechanisms underlying how apoplastic immunity controls... Hosts and pathogens are engaged in a continuous evolutionary struggle for physiological dominance. A major site of this struggle is the apoplast. In -soybean... |
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SubjectTerms | Apoplast Aspartic Acid Endopeptidases - genetics Aspartic Acid Endopeptidases - metabolism Aspartic endopeptidase Binding Biological Sciences Cellulase - genetics Cellulase - metabolism Disease Resistance - genetics Endoglucanase Gene Knockdown Techniques Glycine max - enzymology Glycine max - genetics Glycine max - microbiology Glycosylation Host-Pathogen Interactions - genetics Pathogens Phytophthora - metabolism Phytophthora - pathogenicity Phytophthora sojae Plant Diseases - microbiology Plant Proteins - genetics Plant Proteins - metabolism Plants, Genetically Modified Protease Protein Binding Protein Processing, Post-Translational Proteolysis Soybeans Virulence |
Title | N-glycosylation shields Phytophthora sojae apoplastic effector PsXEG1 from a specific host aspartic protease |
URI | https://www.jstor.org/stable/26970951 https://www.ncbi.nlm.nih.gov/pubmed/33082226 https://www.proquest.com/docview/2458971639 https://www.proquest.com/docview/2452983469 https://pubmed.ncbi.nlm.nih.gov/PMC7959567 |
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