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A transcriptomic snapshot of early molecular communication between Pasteuria penetrans and Meloidogyne incognita
Authors
A Clark
AF Bird
+117 more
AG Whitehead
AJ van Rossum
AN Nathoo
AR Hipkiss
AR Quinlan
B Boettner
B Ketterer
B Li
B Mannervik
B Raymond
C The
CA Perrett
CA Reinitz
CD Sifri
D Wong
DL McEwan
E Moreno-Arriola
E Peter
EE Penhoet
EL Pavlova
ES Kim
FA Partridge
FX Yu
G Simons
H Li
HR Nicholas
I Mohr
IK Vagelas
IR Cohen
Irene Bricchi
J Heino
J Papadopoulou
J Tang
J. P. Yan
JA Melo
JF Preston
K Hesp
K Kim
K. G. DAVIES
Keith G. Davies
KG Bankar
KG Davies
KG Davies
KG Davies
KG Davies
KH Nomura
KJ Livak
L Charles
L Lambrechts
L Lambrechts
LB Cohen
LE Waggoner
M Cohen
M Klass
MA Bakowski
MA Miller
ME Feder
MG Grabherr
MJ Gravato-Nobre
MR Calgaro
MS Gami
MS Kwa
N Borghi
N Kogata
N Lane
N Schormann
N Tavernarakis
N Tavernarakis
N Vibanco-P’erez
O Silva-García
P Abad
P. B. Szecsi
PE Kuwabara
PE Urwin
PK Papolu
PM Brophy
PM Brophy
PM Guimaraes
R Erion
R Roberts
RK Patel
RM Sayre
Rohit N. Shukla
S Anders
S Choi
S Das
S Echevarria-Zomeno
S Mahajan-Miklos
SC Johnson
SC Zevian
SE Chang
SF Altschul
SHE Kaufmann
SJ McTaggart
SM Barribeau
TE Hewlett
TJ Krieger
TL Dunbar
TM Kubiak
TM Roberts
TM Shinnick
U Rao
Uma Rao
V Giguere
V Phani
V Phani
V Phani
Victor Phani
Victor Phani
Vishal S. Somvanshi
X Chen
X Zou
Y Gonskikh
Y Moriya
Y Spiegel
Y Yarden
Y Zhang
Publication date
1 November 2018
Publisher
'Springer Science and Business Media LLC'
Doi
Abstract
© The Author(s). 2018Background: 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.Peer reviewedFinal Published versio
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University of Hertfordshire Research Archive
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