Cargando…

Suppression of Laccase 2 severely impairs cuticle tanning and pathogen resistance during the pupal metamorphosis of Anopheles sinensis (Diptera: Culicidae)

BACKGROUND: Phenol oxidases (POs) catalyze the oxidation of dopa and dopamine to melanin, which is crucial for cuticle formation and innate immune maintenance in insects. Although, Laccase 2, a member of the PO family, has been reported to be a requirement for melanin-mediated cuticle tanning in the...

Descripción completa

Detalles Bibliográficos
Autores principales: Du, Ming-Hui, Yan, Zheng-Wen, Hao, You-Jin, Yan, Zhen-Tian, Si, Feng-Ling, Chen, Bin, Qiao, Liang
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5381134/
https://www.ncbi.nlm.nih.gov/pubmed/28376914
http://dx.doi.org/10.1186/s13071-017-2118-4
_version_ 1782519879029489664
author Du, Ming-Hui
Yan, Zheng-Wen
Hao, You-Jin
Yan, Zhen-Tian
Si, Feng-Ling
Chen, Bin
Qiao, Liang
author_facet Du, Ming-Hui
Yan, Zheng-Wen
Hao, You-Jin
Yan, Zhen-Tian
Si, Feng-Ling
Chen, Bin
Qiao, Liang
author_sort Du, Ming-Hui
collection PubMed
description BACKGROUND: Phenol oxidases (POs) catalyze the oxidation of dopa and dopamine to melanin, which is crucial for cuticle formation and innate immune maintenance in insects. Although, Laccase 2, a member of the PO family, has been reported to be a requirement for melanin-mediated cuticle tanning in the development stages of some insects, whether it participates in cuticle construction and other physiological processes during the metamorphosis of mosquito pupae is unclear. METHODS: The association between the phenotype and the expression profile of Anopheles sinensis Laccase 2 (AsLac2) was assessed from pupation to adult eclosion. Individuals showing an expression deficiency of AsLac2 that was produced by RNAi and their phenotypic defects and physiological characterizations were compared in detail with the controls. RESULTS: During the dominant expression period, knockdown of AsLac2 in pupae caused the cuticle to be unpigmented, and produced thin and very soft cuticles, which further impeded the eclosion rate of adults as well as their fitness. Moreover, melanization immune responses in the pupae were sharply decreased, leading to poor resistance to microorganism infection. Both the high conservation among Laccase 2 homologs and a very similar genomic synteny of the neighborhood in Anopheles genus implies a conservative function in the pupal stage. CONCLUSIONS: To our knowledge, this is the first study to report the serious phenotypic defects in mosquito pupae caused by the dysfunction of Laccase 2. Our findings strongly suggest that Laccase 2 is crucial for Anopheles cuticle construction and melanization immune responses to pathogen infections during pupal metamorphosis. This irreplaceability provides valuable information on the application of Lacccase 2 and/or other key genes in the melanin metabolism pathway for developing mosquito control strategies. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s13071-017-2118-4) contains supplementary material, which is available to authorized users.
format Online
Article
Text
id pubmed-5381134
institution National Center for Biotechnology Information
language English
publishDate 2017
publisher BioMed Central
record_format MEDLINE/PubMed
spelling pubmed-53811342017-04-10 Suppression of Laccase 2 severely impairs cuticle tanning and pathogen resistance during the pupal metamorphosis of Anopheles sinensis (Diptera: Culicidae) Du, Ming-Hui Yan, Zheng-Wen Hao, You-Jin Yan, Zhen-Tian Si, Feng-Ling Chen, Bin Qiao, Liang Parasit Vectors Research BACKGROUND: Phenol oxidases (POs) catalyze the oxidation of dopa and dopamine to melanin, which is crucial for cuticle formation and innate immune maintenance in insects. Although, Laccase 2, a member of the PO family, has been reported to be a requirement for melanin-mediated cuticle tanning in the development stages of some insects, whether it participates in cuticle construction and other physiological processes during the metamorphosis of mosquito pupae is unclear. METHODS: The association between the phenotype and the expression profile of Anopheles sinensis Laccase 2 (AsLac2) was assessed from pupation to adult eclosion. Individuals showing an expression deficiency of AsLac2 that was produced by RNAi and their phenotypic defects and physiological characterizations were compared in detail with the controls. RESULTS: During the dominant expression period, knockdown of AsLac2 in pupae caused the cuticle to be unpigmented, and produced thin and very soft cuticles, which further impeded the eclosion rate of adults as well as their fitness. Moreover, melanization immune responses in the pupae were sharply decreased, leading to poor resistance to microorganism infection. Both the high conservation among Laccase 2 homologs and a very similar genomic synteny of the neighborhood in Anopheles genus implies a conservative function in the pupal stage. CONCLUSIONS: To our knowledge, this is the first study to report the serious phenotypic defects in mosquito pupae caused by the dysfunction of Laccase 2. Our findings strongly suggest that Laccase 2 is crucial for Anopheles cuticle construction and melanization immune responses to pathogen infections during pupal metamorphosis. This irreplaceability provides valuable information on the application of Lacccase 2 and/or other key genes in the melanin metabolism pathway for developing mosquito control strategies. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s13071-017-2118-4) contains supplementary material, which is available to authorized users. BioMed Central 2017-04-04 /pmc/articles/PMC5381134/ /pubmed/28376914 http://dx.doi.org/10.1186/s13071-017-2118-4 Text en © The Author(s). 2017 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
Du, Ming-Hui
Yan, Zheng-Wen
Hao, You-Jin
Yan, Zhen-Tian
Si, Feng-Ling
Chen, Bin
Qiao, Liang
Suppression of Laccase 2 severely impairs cuticle tanning and pathogen resistance during the pupal metamorphosis of Anopheles sinensis (Diptera: Culicidae)
title Suppression of Laccase 2 severely impairs cuticle tanning and pathogen resistance during the pupal metamorphosis of Anopheles sinensis (Diptera: Culicidae)
title_full Suppression of Laccase 2 severely impairs cuticle tanning and pathogen resistance during the pupal metamorphosis of Anopheles sinensis (Diptera: Culicidae)
title_fullStr Suppression of Laccase 2 severely impairs cuticle tanning and pathogen resistance during the pupal metamorphosis of Anopheles sinensis (Diptera: Culicidae)
title_full_unstemmed Suppression of Laccase 2 severely impairs cuticle tanning and pathogen resistance during the pupal metamorphosis of Anopheles sinensis (Diptera: Culicidae)
title_short Suppression of Laccase 2 severely impairs cuticle tanning and pathogen resistance during the pupal metamorphosis of Anopheles sinensis (Diptera: Culicidae)
title_sort suppression of laccase 2 severely impairs cuticle tanning and pathogen resistance during the pupal metamorphosis of anopheles sinensis (diptera: culicidae)
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5381134/
https://www.ncbi.nlm.nih.gov/pubmed/28376914
http://dx.doi.org/10.1186/s13071-017-2118-4
work_keys_str_mv AT duminghui suppressionoflaccase2severelyimpairscuticletanningandpathogenresistanceduringthepupalmetamorphosisofanophelessinensisdipteraculicidae
AT yanzhengwen suppressionoflaccase2severelyimpairscuticletanningandpathogenresistanceduringthepupalmetamorphosisofanophelessinensisdipteraculicidae
AT haoyoujin suppressionoflaccase2severelyimpairscuticletanningandpathogenresistanceduringthepupalmetamorphosisofanophelessinensisdipteraculicidae
AT yanzhentian suppressionoflaccase2severelyimpairscuticletanningandpathogenresistanceduringthepupalmetamorphosisofanophelessinensisdipteraculicidae
AT sifengling suppressionoflaccase2severelyimpairscuticletanningandpathogenresistanceduringthepupalmetamorphosisofanophelessinensisdipteraculicidae
AT chenbin suppressionoflaccase2severelyimpairscuticletanningandpathogenresistanceduringthepupalmetamorphosisofanophelessinensisdipteraculicidae
AT qiaoliang suppressionoflaccase2severelyimpairscuticletanningandpathogenresistanceduringthepupalmetamorphosisofanophelessinensisdipteraculicidae