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Genome sequence and spore germination-associated transcriptome analysis of Corynespora cassiicola from cucumber

BACKGROUND: Corynespora cassiicola, as a necrotrophic phytopathogenic ascomycetous fungus, can infect hundreds of species of plants and rarely causes human diseases. This pathogen infects cucumber species and causes cucumber target spot, which has recently caused large cucumber yield losses in China...

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Autores principales: Gao, Shigang, Zeng, Rong, Xu, Lihui, Song, Zhiwei, Gao, Ping, Dai, Fuming
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7346487/
https://www.ncbi.nlm.nih.gov/pubmed/32641051
http://dx.doi.org/10.1186/s12866-020-01873-w
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author Gao, Shigang
Zeng, Rong
Xu, Lihui
Song, Zhiwei
Gao, Ping
Dai, Fuming
author_facet Gao, Shigang
Zeng, Rong
Xu, Lihui
Song, Zhiwei
Gao, Ping
Dai, Fuming
author_sort Gao, Shigang
collection PubMed
description BACKGROUND: Corynespora cassiicola, as a necrotrophic phytopathogenic ascomycetous fungus, can infect hundreds of species of plants and rarely causes human diseases. This pathogen infects cucumber species and causes cucumber target spot, which has recently caused large cucumber yield losses in China. Genome sequence and spore germination-associated transcriptome analysis will contribute to the understanding of the molecular mechanism of pathogenicity and spore germination of C. cassiicola. RESULTS: First, we reported the draft genome sequences of the cucumber-sampled C. cassiicola isolate HGCC with high virulence. Although conspecific, HGCC exhibited distinct genome sequence differences from a rubber tree-sampled isolate (CCP) and a human-sampled isolate (UM591). The proportion of secreted proteins was 7.2% in HGCC. A total of 28.9% (4232) of HGCC genes, 29.5% (4298) of CCP genes and 28.6% (4214) of UM591 genes were highly homologous to experimentally proven virulence-associated genes, respectively, which were not significantly different (P = 0.866) from the average (29.7%) of 10 other phytopathogenic fungi. Thousands of putative virulence-associated genes in various pathways or families were identified in C. cassiicola. Second, a global view of the transcriptome of C. cassiicola spores during germination was evaluated using RNA sequencing (RNA-Seq). A total of 3288 differentially expressed genes (DEGs) were identified. The majority of KEGG-annotated DEGs were involved in metabolism, genetic information processing, cellular processes, the organismal system, human diseases and environmental information processing. CONCLUSIONS: These results facilitate the exploration of the molecular pathogenic mechanism of C. cassiicola in cucumbers and the understanding of molecular and cellular processes during spore germination.
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spelling pubmed-73464872020-07-14 Genome sequence and spore germination-associated transcriptome analysis of Corynespora cassiicola from cucumber Gao, Shigang Zeng, Rong Xu, Lihui Song, Zhiwei Gao, Ping Dai, Fuming BMC Microbiol Research Article BACKGROUND: Corynespora cassiicola, as a necrotrophic phytopathogenic ascomycetous fungus, can infect hundreds of species of plants and rarely causes human diseases. This pathogen infects cucumber species and causes cucumber target spot, which has recently caused large cucumber yield losses in China. Genome sequence and spore germination-associated transcriptome analysis will contribute to the understanding of the molecular mechanism of pathogenicity and spore germination of C. cassiicola. RESULTS: First, we reported the draft genome sequences of the cucumber-sampled C. cassiicola isolate HGCC with high virulence. Although conspecific, HGCC exhibited distinct genome sequence differences from a rubber tree-sampled isolate (CCP) and a human-sampled isolate (UM591). The proportion of secreted proteins was 7.2% in HGCC. A total of 28.9% (4232) of HGCC genes, 29.5% (4298) of CCP genes and 28.6% (4214) of UM591 genes were highly homologous to experimentally proven virulence-associated genes, respectively, which were not significantly different (P = 0.866) from the average (29.7%) of 10 other phytopathogenic fungi. Thousands of putative virulence-associated genes in various pathways or families were identified in C. cassiicola. Second, a global view of the transcriptome of C. cassiicola spores during germination was evaluated using RNA sequencing (RNA-Seq). A total of 3288 differentially expressed genes (DEGs) were identified. The majority of KEGG-annotated DEGs were involved in metabolism, genetic information processing, cellular processes, the organismal system, human diseases and environmental information processing. CONCLUSIONS: These results facilitate the exploration of the molecular pathogenic mechanism of C. cassiicola in cucumbers and the understanding of molecular and cellular processes during spore germination. BioMed Central 2020-07-08 /pmc/articles/PMC7346487/ /pubmed/32641051 http://dx.doi.org/10.1186/s12866-020-01873-w Text en © The Author(s) 2020 Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
spellingShingle Research Article
Gao, Shigang
Zeng, Rong
Xu, Lihui
Song, Zhiwei
Gao, Ping
Dai, Fuming
Genome sequence and spore germination-associated transcriptome analysis of Corynespora cassiicola from cucumber
title Genome sequence and spore germination-associated transcriptome analysis of Corynespora cassiicola from cucumber
title_full Genome sequence and spore germination-associated transcriptome analysis of Corynespora cassiicola from cucumber
title_fullStr Genome sequence and spore germination-associated transcriptome analysis of Corynespora cassiicola from cucumber
title_full_unstemmed Genome sequence and spore germination-associated transcriptome analysis of Corynespora cassiicola from cucumber
title_short Genome sequence and spore germination-associated transcriptome analysis of Corynespora cassiicola from cucumber
title_sort genome sequence and spore germination-associated transcriptome analysis of corynespora cassiicola from cucumber
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7346487/
https://www.ncbi.nlm.nih.gov/pubmed/32641051
http://dx.doi.org/10.1186/s12866-020-01873-w
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