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The effects of plant cysteine proteinases on the nematode cuticle

BACKGROUND: Plant-derived cysteine proteinases of the papain family (CPs) attack nematodes by digesting the cuticle, leading to rupture and death of the worm. The nematode cuticle is composed of collagens and cuticlins, but the specific molecular target(s) for the proteinases have yet to be identifi...

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Autores principales: Njom, Victor S., Winks, Tim, Diallo, Oumu, Lowe, Ann, Behnke, Jerzy, Dickman, Mark J., Duce, Ian, Johnstone, Iain, Buttle, David J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8180098/
https://www.ncbi.nlm.nih.gov/pubmed/34090505
http://dx.doi.org/10.1186/s13071-021-04800-8
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author Njom, Victor S.
Winks, Tim
Diallo, Oumu
Lowe, Ann
Behnke, Jerzy
Dickman, Mark J.
Duce, Ian
Johnstone, Iain
Buttle, David J.
author_facet Njom, Victor S.
Winks, Tim
Diallo, Oumu
Lowe, Ann
Behnke, Jerzy
Dickman, Mark J.
Duce, Ian
Johnstone, Iain
Buttle, David J.
author_sort Njom, Victor S.
collection PubMed
description BACKGROUND: Plant-derived cysteine proteinases of the papain family (CPs) attack nematodes by digesting the cuticle, leading to rupture and death of the worm. The nematode cuticle is composed of collagens and cuticlins, but the specific molecular target(s) for the proteinases have yet to be identified. METHODS: This study followed the course of nematode cuticle disruption using immunohistochemistry, scanning electron microscopy and proteomics, using a free-living nematode, Caenorhabditis elegans and the murine GI nematode Heligmosomoides bakeri (H. polygyrus) as target organisms. RESULTS: Immunohistochemistry indicated that DPY-7 collagen is a target for CPs on the cuticle of C. elegans. The time course of loss of DPY-7 from the cuticle allowed us to use it to visualise the process of cuticle disruption. There was a marked difference in the time course of damage to the cuticles of the two species of nematode, with H. bakeri being more rapidly hydrolysed. In general, the CPs’ mode of attack on the nematode cuticle was by degrading the structural proteins, leading to loss of integrity of the cuticle, and finally death of the nematode. Proteomic analysis failed conclusively to identify structural targets for CPs, but preliminary data suggested that COL-87 and CUT-19 may be important targets for the CPs, the digestion of which may contribute to cuticle disruption and death of the worm. Cuticle globin was also identified as a cuticular target. The presence of more than one target protein may slow the development of resistance against this new class of anthelmintic. CONCLUSIONS: Scanning electron microscopy and immunohistochemistry allowed the process of disruption of the cuticle to be followed with time. Cuticle collagens and cuticlins are molecular targets for plant cysteine proteinases. However, the presence of tyrosine cross-links in nematode cuticle proteins seriously impeded protein identification by proteomic analyses. Multiple cuticle targets exist, probably making resistance to this new anthelmintic slow to develop. GRAPHIC ABSTRACT: [Image: see text] SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s13071-021-04800-8.
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spelling pubmed-81800982021-06-07 The effects of plant cysteine proteinases on the nematode cuticle Njom, Victor S. Winks, Tim Diallo, Oumu Lowe, Ann Behnke, Jerzy Dickman, Mark J. Duce, Ian Johnstone, Iain Buttle, David J. Parasit Vectors Research BACKGROUND: Plant-derived cysteine proteinases of the papain family (CPs) attack nematodes by digesting the cuticle, leading to rupture and death of the worm. The nematode cuticle is composed of collagens and cuticlins, but the specific molecular target(s) for the proteinases have yet to be identified. METHODS: This study followed the course of nematode cuticle disruption using immunohistochemistry, scanning electron microscopy and proteomics, using a free-living nematode, Caenorhabditis elegans and the murine GI nematode Heligmosomoides bakeri (H. polygyrus) as target organisms. RESULTS: Immunohistochemistry indicated that DPY-7 collagen is a target for CPs on the cuticle of C. elegans. The time course of loss of DPY-7 from the cuticle allowed us to use it to visualise the process of cuticle disruption. There was a marked difference in the time course of damage to the cuticles of the two species of nematode, with H. bakeri being more rapidly hydrolysed. In general, the CPs’ mode of attack on the nematode cuticle was by degrading the structural proteins, leading to loss of integrity of the cuticle, and finally death of the nematode. Proteomic analysis failed conclusively to identify structural targets for CPs, but preliminary data suggested that COL-87 and CUT-19 may be important targets for the CPs, the digestion of which may contribute to cuticle disruption and death of the worm. Cuticle globin was also identified as a cuticular target. The presence of more than one target protein may slow the development of resistance against this new class of anthelmintic. CONCLUSIONS: Scanning electron microscopy and immunohistochemistry allowed the process of disruption of the cuticle to be followed with time. Cuticle collagens and cuticlins are molecular targets for plant cysteine proteinases. However, the presence of tyrosine cross-links in nematode cuticle proteins seriously impeded protein identification by proteomic analyses. Multiple cuticle targets exist, probably making resistance to this new anthelmintic slow to develop. GRAPHIC ABSTRACT: [Image: see text] SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s13071-021-04800-8. BioMed Central 2021-06-05 /pmc/articles/PMC8180098/ /pubmed/34090505 http://dx.doi.org/10.1186/s13071-021-04800-8 Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/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/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://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
Njom, Victor S.
Winks, Tim
Diallo, Oumu
Lowe, Ann
Behnke, Jerzy
Dickman, Mark J.
Duce, Ian
Johnstone, Iain
Buttle, David J.
The effects of plant cysteine proteinases on the nematode cuticle
title The effects of plant cysteine proteinases on the nematode cuticle
title_full The effects of plant cysteine proteinases on the nematode cuticle
title_fullStr The effects of plant cysteine proteinases on the nematode cuticle
title_full_unstemmed The effects of plant cysteine proteinases on the nematode cuticle
title_short The effects of plant cysteine proteinases on the nematode cuticle
title_sort effects of plant cysteine proteinases on the nematode cuticle
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8180098/
https://www.ncbi.nlm.nih.gov/pubmed/34090505
http://dx.doi.org/10.1186/s13071-021-04800-8
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