Identification and Characterization of the Most Abundant Cellulases in Stylet Secretions from Globodera rostochiensis

Plant-parasitic cyst nematodes secrete cell wall modifying proteins during their invasion of host plants. In this study, we used a monoclonal antibody to immunopurify and to sequence the N terminus of the most abundant cellulases in stylet secretions of preparasitic juveniles of Globodera rostochiensis. The N-terminal amino acid sequence perfectly matched the sequence of an expressed sequence tag of two nearly identical genes, named Gr-eng3 and Gr-eng4, which show relatively low similarity with the previously identified Gr-eng1 and Gr-eng2 (i.e., 62% similarity and 42% identity). The recombinantly produced proteins from Gr-eng3 and Gr-eng4 demonstrated specific activity on carboxymethylcellulose, indicating that these genes encode active cellulases. To date, the cellulases in cyst nematodes are comprised of three possible domain structure variants with different types of ancillary domains at the C terminus of the glycosyl hydrolase family 5 (GHF5) domain. We used Bayesian inference to show that the phylogeny of the GHF5 domain based on currently available data suggest that the extant nematode cellulases arose through reshuffling of the GHF5 domain with different types of ancillary domains as relatively independent units. Knocking-down Gr-eng3 and Gr-eng4 using RNA interference resulted in a reduction of nematode infectivity by 57%. Our observations show that the reduced infectivity of the nematodes can be attributed to poor penetration of the host's root system at the onset of parasitism

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Main Authors: Rehman, S., Butterbach, P.B.E., Popeijus, H.E., Overmars, H.A., Davis, E.L., Jones, J.T., Goverse, A., Bakker, J., Smant, G.
Format: Article/Letter to editor biblioteca
Language:English
Subjects:beta-1,4-endoglucanase genes, cell-walls, degradation, expression, heterodera-glycines, meloidogyne-incognita, origin, parasitism, potato cyst-nematode, proteins,
Online Access:https://research.wur.nl/en/publications/identification-and-characterization-of-the-most-abundant-cellulas
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spelling dig-wur-nl-wurpubs-3851142024-09-23 Rehman, S. Butterbach, P.B.E. Popeijus, H.E. Overmars, H.A. Davis, E.L. Jones, J.T. Goverse, A. Bakker, J. Smant, G. Article/Letter to editor Phytopathology 99 (2009) 2 ISSN: 0031-949X Identification and Characterization of the Most Abundant Cellulases in Stylet Secretions from Globodera rostochiensis 2009 Plant-parasitic cyst nematodes secrete cell wall modifying proteins during their invasion of host plants. In this study, we used a monoclonal antibody to immunopurify and to sequence the N terminus of the most abundant cellulases in stylet secretions of preparasitic juveniles of Globodera rostochiensis. The N-terminal amino acid sequence perfectly matched the sequence of an expressed sequence tag of two nearly identical genes, named Gr-eng3 and Gr-eng4, which show relatively low similarity with the previously identified Gr-eng1 and Gr-eng2 (i.e., 62% similarity and 42% identity). The recombinantly produced proteins from Gr-eng3 and Gr-eng4 demonstrated specific activity on carboxymethylcellulose, indicating that these genes encode active cellulases. To date, the cellulases in cyst nematodes are comprised of three possible domain structure variants with different types of ancillary domains at the C terminus of the glycosyl hydrolase family 5 (GHF5) domain. We used Bayesian inference to show that the phylogeny of the GHF5 domain based on currently available data suggest that the extant nematode cellulases arose through reshuffling of the GHF5 domain with different types of ancillary domains as relatively independent units. Knocking-down Gr-eng3 and Gr-eng4 using RNA interference resulted in a reduction of nematode infectivity by 57%. Our observations show that the reduced infectivity of the nematodes can be attributed to poor penetration of the host's root system at the onset of parasitism en application/pdf https://research.wur.nl/en/publications/identification-and-characterization-of-the-most-abundant-cellulas 10.1094/PHYTO-99-2-0194 https://edepot.wur.nl/16191 beta-1,4-endoglucanase genes cell-walls degradation expression heterodera-glycines meloidogyne-incognita origin parasitism potato cyst-nematode proteins (c) publisher Wageningen University & Research
institution WUR NL
collection DSpace
country Países bajos
countrycode NL
component Bibliográfico
access En linea
databasecode dig-wur-nl
tag biblioteca
region Europa del Oeste
libraryname WUR Library Netherlands
language English
topic beta-1,4-endoglucanase genes
cell-walls
degradation
expression
heterodera-glycines
meloidogyne-incognita
origin
parasitism
potato cyst-nematode
proteins
beta-1,4-endoglucanase genes
cell-walls
degradation
expression
heterodera-glycines
meloidogyne-incognita
origin
parasitism
potato cyst-nematode
proteins
spellingShingle beta-1,4-endoglucanase genes
cell-walls
degradation
expression
heterodera-glycines
meloidogyne-incognita
origin
parasitism
potato cyst-nematode
proteins
beta-1,4-endoglucanase genes
cell-walls
degradation
expression
heterodera-glycines
meloidogyne-incognita
origin
parasitism
potato cyst-nematode
proteins
Rehman, S.
Butterbach, P.B.E.
Popeijus, H.E.
Overmars, H.A.
Davis, E.L.
Jones, J.T.
Goverse, A.
Bakker, J.
Smant, G.
Identification and Characterization of the Most Abundant Cellulases in Stylet Secretions from Globodera rostochiensis
description Plant-parasitic cyst nematodes secrete cell wall modifying proteins during their invasion of host plants. In this study, we used a monoclonal antibody to immunopurify and to sequence the N terminus of the most abundant cellulases in stylet secretions of preparasitic juveniles of Globodera rostochiensis. The N-terminal amino acid sequence perfectly matched the sequence of an expressed sequence tag of two nearly identical genes, named Gr-eng3 and Gr-eng4, which show relatively low similarity with the previously identified Gr-eng1 and Gr-eng2 (i.e., 62% similarity and 42% identity). The recombinantly produced proteins from Gr-eng3 and Gr-eng4 demonstrated specific activity on carboxymethylcellulose, indicating that these genes encode active cellulases. To date, the cellulases in cyst nematodes are comprised of three possible domain structure variants with different types of ancillary domains at the C terminus of the glycosyl hydrolase family 5 (GHF5) domain. We used Bayesian inference to show that the phylogeny of the GHF5 domain based on currently available data suggest that the extant nematode cellulases arose through reshuffling of the GHF5 domain with different types of ancillary domains as relatively independent units. Knocking-down Gr-eng3 and Gr-eng4 using RNA interference resulted in a reduction of nematode infectivity by 57%. Our observations show that the reduced infectivity of the nematodes can be attributed to poor penetration of the host's root system at the onset of parasitism
format Article/Letter to editor
topic_facet beta-1,4-endoglucanase genes
cell-walls
degradation
expression
heterodera-glycines
meloidogyne-incognita
origin
parasitism
potato cyst-nematode
proteins
author Rehman, S.
Butterbach, P.B.E.
Popeijus, H.E.
Overmars, H.A.
Davis, E.L.
Jones, J.T.
Goverse, A.
Bakker, J.
Smant, G.
author_facet Rehman, S.
Butterbach, P.B.E.
Popeijus, H.E.
Overmars, H.A.
Davis, E.L.
Jones, J.T.
Goverse, A.
Bakker, J.
Smant, G.
author_sort Rehman, S.
title Identification and Characterization of the Most Abundant Cellulases in Stylet Secretions from Globodera rostochiensis
title_short Identification and Characterization of the Most Abundant Cellulases in Stylet Secretions from Globodera rostochiensis
title_full Identification and Characterization of the Most Abundant Cellulases in Stylet Secretions from Globodera rostochiensis
title_fullStr Identification and Characterization of the Most Abundant Cellulases in Stylet Secretions from Globodera rostochiensis
title_full_unstemmed Identification and Characterization of the Most Abundant Cellulases in Stylet Secretions from Globodera rostochiensis
title_sort identification and characterization of the most abundant cellulases in stylet secretions from globodera rostochiensis
url https://research.wur.nl/en/publications/identification-and-characterization-of-the-most-abundant-cellulas
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