Cargando…

Comparative genomic analysis of monosporidial and monoteliosporic cultures for unraveling the complexity of molecular pathogenesis of Tilletia indica pathogen of wheat

Tilletia indica (Ti) - a quarantined fungal pathogen of wheat and its pathogenesis is chiefly governed by pathogen effectors secreted inside the host plant. The de novo genome sequencing of several field isolates and stages available could be used for understanding the molecular pathogenesis. The pr...

Descripción completa

Detalles Bibliográficos
Autores principales: Mishra, Pallavi, Maurya, Ranjeet, Gupta, Vijai K., Ramteke, Pramod W., Marla, Soma S., Kumar, Anil
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6547692/
https://www.ncbi.nlm.nih.gov/pubmed/31160715
http://dx.doi.org/10.1038/s41598-019-44464-0
_version_ 1783423734149808128
author Mishra, Pallavi
Maurya, Ranjeet
Gupta, Vijai K.
Ramteke, Pramod W.
Marla, Soma S.
Kumar, Anil
author_facet Mishra, Pallavi
Maurya, Ranjeet
Gupta, Vijai K.
Ramteke, Pramod W.
Marla, Soma S.
Kumar, Anil
author_sort Mishra, Pallavi
collection PubMed
description Tilletia indica (Ti) - a quarantined fungal pathogen of wheat and its pathogenesis is chiefly governed by pathogen effectors secreted inside the host plant. The de novo genome sequencing of several field isolates and stages available could be used for understanding the molecular pathogenesis. The presence of gaps and low coverage of assembled genomes poses a problem in accurate functional annotation of such functions. In the present study attempts were made to improve the Ti draft genome through reconciliation of globally available datasets of three highly virulent monoteliospore cultures of Ti field isolates. It has sequence depth of 107x and N50 scaffold size of 80,772 (more than 26 times as large as achieved in the draft assembly) with highest sequence contiguity, more accurate and nearly complete. Functional annotation revealed that Ti genome contains 9209 genes evolved with many expanded gene families and arranged mostly in a cluster. About 79% of Ti genes were orthologous to other basidiomycetes fungi, Around 7.93% proteins were having secretary signals and 6.66% were identified as highly virulent pathogenicity genes. Using improved Ti genome as a reference, the genomic variation was assessed with respect to repeats, SNPs/InDel, gene families and correct set of virulence associated genes during its life cycle. The comparative intra-species, inter-stage and inter-species genomic variation will have broader implications to understand the gene regulatory networks involved in growth, mating and virulence behaviour of Tilletia f. spp. and also for better appreciation of fungal biology and disease management.
format Online
Article
Text
id pubmed-6547692
institution National Center for Biotechnology Information
language English
publishDate 2019
publisher Nature Publishing Group UK
record_format MEDLINE/PubMed
spelling pubmed-65476922019-06-10 Comparative genomic analysis of monosporidial and monoteliosporic cultures for unraveling the complexity of molecular pathogenesis of Tilletia indica pathogen of wheat Mishra, Pallavi Maurya, Ranjeet Gupta, Vijai K. Ramteke, Pramod W. Marla, Soma S. Kumar, Anil Sci Rep Article Tilletia indica (Ti) - a quarantined fungal pathogen of wheat and its pathogenesis is chiefly governed by pathogen effectors secreted inside the host plant. The de novo genome sequencing of several field isolates and stages available could be used for understanding the molecular pathogenesis. The presence of gaps and low coverage of assembled genomes poses a problem in accurate functional annotation of such functions. In the present study attempts were made to improve the Ti draft genome through reconciliation of globally available datasets of three highly virulent monoteliospore cultures of Ti field isolates. It has sequence depth of 107x and N50 scaffold size of 80,772 (more than 26 times as large as achieved in the draft assembly) with highest sequence contiguity, more accurate and nearly complete. Functional annotation revealed that Ti genome contains 9209 genes evolved with many expanded gene families and arranged mostly in a cluster. About 79% of Ti genes were orthologous to other basidiomycetes fungi, Around 7.93% proteins were having secretary signals and 6.66% were identified as highly virulent pathogenicity genes. Using improved Ti genome as a reference, the genomic variation was assessed with respect to repeats, SNPs/InDel, gene families and correct set of virulence associated genes during its life cycle. The comparative intra-species, inter-stage and inter-species genomic variation will have broader implications to understand the gene regulatory networks involved in growth, mating and virulence behaviour of Tilletia f. spp. and also for better appreciation of fungal biology and disease management. Nature Publishing Group UK 2019-06-03 /pmc/articles/PMC6547692/ /pubmed/31160715 http://dx.doi.org/10.1038/s41598-019-44464-0 Text en © The Author(s) 2019 Open Access This 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 license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license 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 license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Mishra, Pallavi
Maurya, Ranjeet
Gupta, Vijai K.
Ramteke, Pramod W.
Marla, Soma S.
Kumar, Anil
Comparative genomic analysis of monosporidial and monoteliosporic cultures for unraveling the complexity of molecular pathogenesis of Tilletia indica pathogen of wheat
title Comparative genomic analysis of monosporidial and monoteliosporic cultures for unraveling the complexity of molecular pathogenesis of Tilletia indica pathogen of wheat
title_full Comparative genomic analysis of monosporidial and monoteliosporic cultures for unraveling the complexity of molecular pathogenesis of Tilletia indica pathogen of wheat
title_fullStr Comparative genomic analysis of monosporidial and monoteliosporic cultures for unraveling the complexity of molecular pathogenesis of Tilletia indica pathogen of wheat
title_full_unstemmed Comparative genomic analysis of monosporidial and monoteliosporic cultures for unraveling the complexity of molecular pathogenesis of Tilletia indica pathogen of wheat
title_short Comparative genomic analysis of monosporidial and monoteliosporic cultures for unraveling the complexity of molecular pathogenesis of Tilletia indica pathogen of wheat
title_sort comparative genomic analysis of monosporidial and monoteliosporic cultures for unraveling the complexity of molecular pathogenesis of tilletia indica pathogen of wheat
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6547692/
https://www.ncbi.nlm.nih.gov/pubmed/31160715
http://dx.doi.org/10.1038/s41598-019-44464-0
work_keys_str_mv AT mishrapallavi comparativegenomicanalysisofmonosporidialandmonoteliosporicculturesforunravelingthecomplexityofmolecularpathogenesisoftilletiaindicapathogenofwheat
AT mauryaranjeet comparativegenomicanalysisofmonosporidialandmonoteliosporicculturesforunravelingthecomplexityofmolecularpathogenesisoftilletiaindicapathogenofwheat
AT guptavijaik comparativegenomicanalysisofmonosporidialandmonoteliosporicculturesforunravelingthecomplexityofmolecularpathogenesisoftilletiaindicapathogenofwheat
AT ramtekepramodw comparativegenomicanalysisofmonosporidialandmonoteliosporicculturesforunravelingthecomplexityofmolecularpathogenesisoftilletiaindicapathogenofwheat
AT marlasomas comparativegenomicanalysisofmonosporidialandmonoteliosporicculturesforunravelingthecomplexityofmolecularpathogenesisoftilletiaindicapathogenofwheat
AT kumaranil comparativegenomicanalysisofmonosporidialandmonoteliosporicculturesforunravelingthecomplexityofmolecularpathogenesisoftilletiaindicapathogenofwheat