Cargando…

Functional Study on Cytochrome P450 in Response to L(−)-Carvone Stress in Bursaphelenchus xylophilus

Bursaphelenchus xylophilus (PWN) causes pine wilt disease (PWD), which is one of the most devastating pine diseases worldwide. Cytochrome P450 (CYP) catalyzes the biosynthetic metabolism of terpenoids and plays an important role in the modification of secondary metabolites in all living organisms. W...

Descripción completa

Detalles Bibliográficos
Autores principales: Chen, Jie, Hao, Xin, Tan, Ruina, Li, Yang, Wang, Bowen, Pan, Jialiang, Ma, Wei, Ma, Ling
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9689654/
https://www.ncbi.nlm.nih.gov/pubmed/36360193
http://dx.doi.org/10.3390/genes13111956
_version_ 1784836589819527168
author Chen, Jie
Hao, Xin
Tan, Ruina
Li, Yang
Wang, Bowen
Pan, Jialiang
Ma, Wei
Ma, Ling
author_facet Chen, Jie
Hao, Xin
Tan, Ruina
Li, Yang
Wang, Bowen
Pan, Jialiang
Ma, Wei
Ma, Ling
author_sort Chen, Jie
collection PubMed
description Bursaphelenchus xylophilus (PWN) causes pine wilt disease (PWD), which is one of the most devastating pine diseases worldwide. Cytochrome P450 (CYP) catalyzes the biosynthetic metabolism of terpenoids and plays an important role in the modification of secondary metabolites in all living organisms. We investigated the molecular characteristics and biological functions of Bx-cyp29A3 in B. xylophilus. The bioinformatics analysis results indicated that Bx-cyp29A3 has a transmembrane domain and could dock with L(−)-carvone. The gene expression pattern indicated that Bx-cyp29A3 was expressed in 0.2, 0.4, 0.6, 0.8, and 1.0 mg/mL L(−)-carvone solutions. The Bx-cyp29A3 expression increased in a dose-dependent manner and peaked at 24 h of exposure when the L(−)-carvone solution concentration was 0.8 mg/mL. However, the gene expression peaked at 0.6 mg/mL after 36 h. Furthermore, RNA interference (RNAi) indicated that Bx-cyp29A3 played an essential role in the response to L(−)-carvone. The mortality rates of the Bx-cyp29A3 knockdown groups were higher than those of the control groups in the 0.4, 0.6, 0.8, and 1.0 mg/mL carvone solutions after 24 h of exposure or 36 h of exposure. In summary, bioinformatics provided the structural characteristics and conserved sequence properties of Bx-cyp29A3 and its encoded protein, which provided a target gene for the study of the P450 family of B. xylophilus. Gene silencing experiments clarified the function of Bx-cyp29A3 in the immune defense of B. xylophilus. This study provides a basis for the screening of new molecular targets for the prevention and management of B. xylophilus.
format Online
Article
Text
id pubmed-9689654
institution National Center for Biotechnology Information
language English
publishDate 2022
publisher MDPI
record_format MEDLINE/PubMed
spelling pubmed-96896542022-11-25 Functional Study on Cytochrome P450 in Response to L(−)-Carvone Stress in Bursaphelenchus xylophilus Chen, Jie Hao, Xin Tan, Ruina Li, Yang Wang, Bowen Pan, Jialiang Ma, Wei Ma, Ling Genes (Basel) Article Bursaphelenchus xylophilus (PWN) causes pine wilt disease (PWD), which is one of the most devastating pine diseases worldwide. Cytochrome P450 (CYP) catalyzes the biosynthetic metabolism of terpenoids and plays an important role in the modification of secondary metabolites in all living organisms. We investigated the molecular characteristics and biological functions of Bx-cyp29A3 in B. xylophilus. The bioinformatics analysis results indicated that Bx-cyp29A3 has a transmembrane domain and could dock with L(−)-carvone. The gene expression pattern indicated that Bx-cyp29A3 was expressed in 0.2, 0.4, 0.6, 0.8, and 1.0 mg/mL L(−)-carvone solutions. The Bx-cyp29A3 expression increased in a dose-dependent manner and peaked at 24 h of exposure when the L(−)-carvone solution concentration was 0.8 mg/mL. However, the gene expression peaked at 0.6 mg/mL after 36 h. Furthermore, RNA interference (RNAi) indicated that Bx-cyp29A3 played an essential role in the response to L(−)-carvone. The mortality rates of the Bx-cyp29A3 knockdown groups were higher than those of the control groups in the 0.4, 0.6, 0.8, and 1.0 mg/mL carvone solutions after 24 h of exposure or 36 h of exposure. In summary, bioinformatics provided the structural characteristics and conserved sequence properties of Bx-cyp29A3 and its encoded protein, which provided a target gene for the study of the P450 family of B. xylophilus. Gene silencing experiments clarified the function of Bx-cyp29A3 in the immune defense of B. xylophilus. This study provides a basis for the screening of new molecular targets for the prevention and management of B. xylophilus. MDPI 2022-10-27 /pmc/articles/PMC9689654/ /pubmed/36360193 http://dx.doi.org/10.3390/genes13111956 Text en © 2022 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Chen, Jie
Hao, Xin
Tan, Ruina
Li, Yang
Wang, Bowen
Pan, Jialiang
Ma, Wei
Ma, Ling
Functional Study on Cytochrome P450 in Response to L(−)-Carvone Stress in Bursaphelenchus xylophilus
title Functional Study on Cytochrome P450 in Response to L(−)-Carvone Stress in Bursaphelenchus xylophilus
title_full Functional Study on Cytochrome P450 in Response to L(−)-Carvone Stress in Bursaphelenchus xylophilus
title_fullStr Functional Study on Cytochrome P450 in Response to L(−)-Carvone Stress in Bursaphelenchus xylophilus
title_full_unstemmed Functional Study on Cytochrome P450 in Response to L(−)-Carvone Stress in Bursaphelenchus xylophilus
title_short Functional Study on Cytochrome P450 in Response to L(−)-Carvone Stress in Bursaphelenchus xylophilus
title_sort functional study on cytochrome p450 in response to l(−)-carvone stress in bursaphelenchus xylophilus
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9689654/
https://www.ncbi.nlm.nih.gov/pubmed/36360193
http://dx.doi.org/10.3390/genes13111956
work_keys_str_mv AT chenjie functionalstudyoncytochromep450inresponsetolcarvonestressinbursaphelenchusxylophilus
AT haoxin functionalstudyoncytochromep450inresponsetolcarvonestressinbursaphelenchusxylophilus
AT tanruina functionalstudyoncytochromep450inresponsetolcarvonestressinbursaphelenchusxylophilus
AT liyang functionalstudyoncytochromep450inresponsetolcarvonestressinbursaphelenchusxylophilus
AT wangbowen functionalstudyoncytochromep450inresponsetolcarvonestressinbursaphelenchusxylophilus
AT panjialiang functionalstudyoncytochromep450inresponsetolcarvonestressinbursaphelenchusxylophilus
AT mawei functionalstudyoncytochromep450inresponsetolcarvonestressinbursaphelenchusxylophilus
AT maling functionalstudyoncytochromep450inresponsetolcarvonestressinbursaphelenchusxylophilus