Cargando…

A transcriptomic snapshot of early molecular communication between Pasteuria penetrans and Meloidogyne incognita

BACKGROUND: Southern root-knot nematode Meloidogyne incognita (Kofoid and White, 1919), Chitwood, 1949 is a key pest of agricultural crops. Pasteuria penetrans is a hyperparasitic bacterium capable of suppressing the nematode reproduction, and represents a typical coevolved pathogen-hyperparasite sy...

Descripción completa

Detalles Bibliográficos
Autores principales: Phani, Victor, Somvanshi, Vishal S., Shukla, Rohit N., Davies, Keith G., Rao, Uma
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6263062/
https://www.ncbi.nlm.nih.gov/pubmed/30486772
http://dx.doi.org/10.1186/s12864-018-5230-8
_version_ 1783375227544141824
author Phani, Victor
Somvanshi, Vishal S.
Shukla, Rohit N.
Davies, Keith G.
Rao, Uma
author_facet Phani, Victor
Somvanshi, Vishal S.
Shukla, Rohit N.
Davies, Keith G.
Rao, Uma
author_sort Phani, Victor
collection PubMed
description BACKGROUND: Southern root-knot nematode Meloidogyne incognita (Kofoid and White, 1919), Chitwood, 1949 is a key pest of agricultural crops. Pasteuria penetrans is a hyperparasitic bacterium capable of suppressing the nematode reproduction, and represents a typical coevolved pathogen-hyperparasite system. Attachment of Pasteuria endospores to the cuticle of second-stage nematode juveniles is the first and pivotal step in the bacterial infection. RNA-Seq was used to understand the early transcriptional response of the root-knot nematode at 8 h post Pasteuria endospore attachment. RESULTS: A total of 52,485 transcripts were assembled from the high quality (HQ) reads, out of which 582 transcripts were found differentially expressed in the Pasteuria endospore encumbered J2 s, of which 229 were up-regulated and 353 were down-regulated. Pasteuria infection caused a suppression of the protein synthesis machinery of the nematode. Several of the differentially expressed transcripts were putatively involved in nematode innate immunity, signaling, stress responses, endospore attachment process and post-attachment behavioral modification of the juveniles. The expression profiles of fifteen selected transcripts were validated to be true by the qRT PCR. RNAi based silencing of transcripts coding for fructose bisphosphate aldolase and glucosyl transferase caused a reduction in endospore attachment as compared to the controls, whereas, silencing of aspartic protease and ubiquitin coding transcripts resulted in higher incidence of endospore attachment on the nematode cuticle. CONCLUSIONS: Here we provide evidence of an early transcriptional response by the nematode upon infection by Pasteuria prior to root invasion. We found that adhesion of Pasteuria endospores to the cuticle induced a down-regulated protein response in the nematode. In addition, we show that fructose bisphosphate aldolase, glucosyl transferase, aspartic protease and ubiquitin coding transcripts are involved in modulating the endospore attachment on the nematode cuticle. Our results add new and significant information to the existing knowledge on early molecular interaction between M. incognita and P. penetrans. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s12864-018-5230-8) contains supplementary material, which is available to authorized users.
format Online
Article
Text
id pubmed-6263062
institution National Center for Biotechnology Information
language English
publishDate 2018
publisher BioMed Central
record_format MEDLINE/PubMed
spelling pubmed-62630622018-12-05 A transcriptomic snapshot of early molecular communication between Pasteuria penetrans and Meloidogyne incognita Phani, Victor Somvanshi, Vishal S. Shukla, Rohit N. Davies, Keith G. Rao, Uma BMC Genomics Research Article BACKGROUND: Southern root-knot nematode Meloidogyne incognita (Kofoid and White, 1919), Chitwood, 1949 is a key pest of agricultural crops. Pasteuria penetrans is a hyperparasitic bacterium capable of suppressing the nematode reproduction, and represents a typical coevolved pathogen-hyperparasite system. Attachment of Pasteuria endospores to the cuticle of second-stage nematode juveniles is the first and pivotal step in the bacterial infection. RNA-Seq was used to understand the early transcriptional response of the root-knot nematode at 8 h post Pasteuria endospore attachment. RESULTS: A total of 52,485 transcripts were assembled from the high quality (HQ) reads, out of which 582 transcripts were found differentially expressed in the Pasteuria endospore encumbered J2 s, of which 229 were up-regulated and 353 were down-regulated. Pasteuria infection caused a suppression of the protein synthesis machinery of the nematode. Several of the differentially expressed transcripts were putatively involved in nematode innate immunity, signaling, stress responses, endospore attachment process and post-attachment behavioral modification of the juveniles. The expression profiles of fifteen selected transcripts were validated to be true by the qRT PCR. RNAi based silencing of transcripts coding for fructose bisphosphate aldolase and glucosyl transferase caused a reduction in endospore attachment as compared to the controls, whereas, silencing of aspartic protease and ubiquitin coding transcripts resulted in higher incidence of endospore attachment on the nematode cuticle. CONCLUSIONS: Here we provide evidence of an early transcriptional response by the nematode upon infection by Pasteuria prior to root invasion. We found that adhesion of Pasteuria endospores to the cuticle induced a down-regulated protein response in the nematode. In addition, we show that fructose bisphosphate aldolase, glucosyl transferase, aspartic protease and ubiquitin coding transcripts are involved in modulating the endospore attachment on the nematode cuticle. Our results add new and significant information to the existing knowledge on early molecular interaction between M. incognita and P. penetrans. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s12864-018-5230-8) contains supplementary material, which is available to authorized users. BioMed Central 2018-11-29 /pmc/articles/PMC6263062/ /pubmed/30486772 http://dx.doi.org/10.1186/s12864-018-5230-8 Text en © The Author(s). 2018 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided 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 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.
spellingShingle Research Article
Phani, Victor
Somvanshi, Vishal S.
Shukla, Rohit N.
Davies, Keith G.
Rao, Uma
A transcriptomic snapshot of early molecular communication between Pasteuria penetrans and Meloidogyne incognita
title A transcriptomic snapshot of early molecular communication between Pasteuria penetrans and Meloidogyne incognita
title_full A transcriptomic snapshot of early molecular communication between Pasteuria penetrans and Meloidogyne incognita
title_fullStr A transcriptomic snapshot of early molecular communication between Pasteuria penetrans and Meloidogyne incognita
title_full_unstemmed A transcriptomic snapshot of early molecular communication between Pasteuria penetrans and Meloidogyne incognita
title_short A transcriptomic snapshot of early molecular communication between Pasteuria penetrans and Meloidogyne incognita
title_sort transcriptomic snapshot of early molecular communication between pasteuria penetrans and meloidogyne incognita
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6263062/
https://www.ncbi.nlm.nih.gov/pubmed/30486772
http://dx.doi.org/10.1186/s12864-018-5230-8
work_keys_str_mv AT phanivictor atranscriptomicsnapshotofearlymolecularcommunicationbetweenpasteuriapenetransandmeloidogyneincognita
AT somvanshivishals atranscriptomicsnapshotofearlymolecularcommunicationbetweenpasteuriapenetransandmeloidogyneincognita
AT shuklarohitn atranscriptomicsnapshotofearlymolecularcommunicationbetweenpasteuriapenetransandmeloidogyneincognita
AT davieskeithg atranscriptomicsnapshotofearlymolecularcommunicationbetweenpasteuriapenetransandmeloidogyneincognita
AT raouma atranscriptomicsnapshotofearlymolecularcommunicationbetweenpasteuriapenetransandmeloidogyneincognita
AT phanivictor transcriptomicsnapshotofearlymolecularcommunicationbetweenpasteuriapenetransandmeloidogyneincognita
AT somvanshivishals transcriptomicsnapshotofearlymolecularcommunicationbetweenpasteuriapenetransandmeloidogyneincognita
AT shuklarohitn transcriptomicsnapshotofearlymolecularcommunicationbetweenpasteuriapenetransandmeloidogyneincognita
AT davieskeithg transcriptomicsnapshotofearlymolecularcommunicationbetweenpasteuriapenetransandmeloidogyneincognita
AT raouma transcriptomicsnapshotofearlymolecularcommunicationbetweenpasteuriapenetransandmeloidogyneincognita