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Comparative genomics and transcriptome analysis reveals potential pathogenic mechanisms of Microdochium paspali on seashore paspalum

The sparse leaf patch of seashore paspalum (Paspalum vaginatum Sw.) caused by Microdochium paspali seriously impacts the landscape value of turf and poses a challenge to the maintenance and management of golf courses. Little is known about the genome of M. paspali or the potential genes underlying p...

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Autores principales: Jin, Peiyuan, Kong, Yixuan, Zhang, Ze, Zhang, Huangwei, Dong, Yinglu, Lamour, Kurt, Yang, Zhimin, Zhou, Yuxin, Hu, Jian
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10546424/
https://www.ncbi.nlm.nih.gov/pubmed/37795300
http://dx.doi.org/10.3389/fmicb.2023.1259241
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author Jin, Peiyuan
Kong, Yixuan
Zhang, Ze
Zhang, Huangwei
Dong, Yinglu
Lamour, Kurt
Yang, Zhimin
Zhou, Yuxin
Hu, Jian
author_facet Jin, Peiyuan
Kong, Yixuan
Zhang, Ze
Zhang, Huangwei
Dong, Yinglu
Lamour, Kurt
Yang, Zhimin
Zhou, Yuxin
Hu, Jian
author_sort Jin, Peiyuan
collection PubMed
description The sparse leaf patch of seashore paspalum (Paspalum vaginatum Sw.) caused by Microdochium paspali seriously impacts the landscape value of turf and poses a challenge to the maintenance and management of golf courses. Little is known about the genome of M. paspali or the potential genes underlying pathogenicity. In this study, we present a high-quality genome assembly of M. paspali with 14 contigs using the Nanopore and Illumina platform. The M. paspali genome is roughly 37.32 Mb in size and contains 10,365 putative protein-coding genes. These encompass a total of 3,830 pathogen-host interactions (PHI) genes, 481 carbohydrate-active enzymes (CAZymes) coding genes, 105 effectors, and 50 secondary metabolite biosynthetic gene clusters (SMGCs) predicted to be associated with pathogenicity. Comparative genomic analysis suggests M. paspali has 672 species-specific genes (SSGs) compared to two previously sequenced non-pathogenic Microdochium species, including 24 species-specific gene clusters (SSGCs). Comparative transcriptomic analyses reveal that 739 PHIs, 198 CAZymes, 40 effectors, 21 SMGCs, 213 SSGs, and 4 SSGCs were significantly up-regulated during the process of infection. In conclusion, the study enriches the genomic resources of Microdochium species and provides a valuable resource to characterize the pathogenic mechanisms of M. paspali.
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spelling pubmed-105464242023-10-04 Comparative genomics and transcriptome analysis reveals potential pathogenic mechanisms of Microdochium paspali on seashore paspalum Jin, Peiyuan Kong, Yixuan Zhang, Ze Zhang, Huangwei Dong, Yinglu Lamour, Kurt Yang, Zhimin Zhou, Yuxin Hu, Jian Front Microbiol Microbiology The sparse leaf patch of seashore paspalum (Paspalum vaginatum Sw.) caused by Microdochium paspali seriously impacts the landscape value of turf and poses a challenge to the maintenance and management of golf courses. Little is known about the genome of M. paspali or the potential genes underlying pathogenicity. In this study, we present a high-quality genome assembly of M. paspali with 14 contigs using the Nanopore and Illumina platform. The M. paspali genome is roughly 37.32 Mb in size and contains 10,365 putative protein-coding genes. These encompass a total of 3,830 pathogen-host interactions (PHI) genes, 481 carbohydrate-active enzymes (CAZymes) coding genes, 105 effectors, and 50 secondary metabolite biosynthetic gene clusters (SMGCs) predicted to be associated with pathogenicity. Comparative genomic analysis suggests M. paspali has 672 species-specific genes (SSGs) compared to two previously sequenced non-pathogenic Microdochium species, including 24 species-specific gene clusters (SSGCs). Comparative transcriptomic analyses reveal that 739 PHIs, 198 CAZymes, 40 effectors, 21 SMGCs, 213 SSGs, and 4 SSGCs were significantly up-regulated during the process of infection. In conclusion, the study enriches the genomic resources of Microdochium species and provides a valuable resource to characterize the pathogenic mechanisms of M. paspali. Frontiers Media S.A. 2023-09-15 /pmc/articles/PMC10546424/ /pubmed/37795300 http://dx.doi.org/10.3389/fmicb.2023.1259241 Text en Copyright © 2023 Jin, Kong, Zhang, Zhang, Dong, Lamour, Yang, Zhou and Hu. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Microbiology
Jin, Peiyuan
Kong, Yixuan
Zhang, Ze
Zhang, Huangwei
Dong, Yinglu
Lamour, Kurt
Yang, Zhimin
Zhou, Yuxin
Hu, Jian
Comparative genomics and transcriptome analysis reveals potential pathogenic mechanisms of Microdochium paspali on seashore paspalum
title Comparative genomics and transcriptome analysis reveals potential pathogenic mechanisms of Microdochium paspali on seashore paspalum
title_full Comparative genomics and transcriptome analysis reveals potential pathogenic mechanisms of Microdochium paspali on seashore paspalum
title_fullStr Comparative genomics and transcriptome analysis reveals potential pathogenic mechanisms of Microdochium paspali on seashore paspalum
title_full_unstemmed Comparative genomics and transcriptome analysis reveals potential pathogenic mechanisms of Microdochium paspali on seashore paspalum
title_short Comparative genomics and transcriptome analysis reveals potential pathogenic mechanisms of Microdochium paspali on seashore paspalum
title_sort comparative genomics and transcriptome analysis reveals potential pathogenic mechanisms of microdochium paspali on seashore paspalum
topic Microbiology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10546424/
https://www.ncbi.nlm.nih.gov/pubmed/37795300
http://dx.doi.org/10.3389/fmicb.2023.1259241
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