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Protein interaction networks at the host–microbe interface in Diaphorina citri, the insect vector of the citrus greening pathogen

The Asian citrus psyllid (Diaphorina citri) is the insect vector responsible for the worldwide spread of ‘Candidatus Liberibacter asiaticus’ (CLas), the bacterial pathogen associated with citrus greening disease. Developmental changes in the insect vector impact pathogen transmission, such that D. c...

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Autores principales: Ramsey, J. S., Chavez, J. D., Johnson, R., Hosseinzadeh, S., Mahoney, J. E., Mohr, J. P., Robison, F., Zhong, X., Hall, D. G., MacCoss, M., Bruce, J., Cilia, M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Royal Society Publishing 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5367280/
https://www.ncbi.nlm.nih.gov/pubmed/28386418
http://dx.doi.org/10.1098/rsos.160545
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author Ramsey, J. S.
Chavez, J. D.
Johnson, R.
Hosseinzadeh, S.
Mahoney, J. E.
Mohr, J. P.
Robison, F.
Zhong, X.
Hall, D. G.
MacCoss, M.
Bruce, J.
Cilia, M.
author_facet Ramsey, J. S.
Chavez, J. D.
Johnson, R.
Hosseinzadeh, S.
Mahoney, J. E.
Mohr, J. P.
Robison, F.
Zhong, X.
Hall, D. G.
MacCoss, M.
Bruce, J.
Cilia, M.
author_sort Ramsey, J. S.
collection PubMed
description The Asian citrus psyllid (Diaphorina citri) is the insect vector responsible for the worldwide spread of ‘Candidatus Liberibacter asiaticus’ (CLas), the bacterial pathogen associated with citrus greening disease. Developmental changes in the insect vector impact pathogen transmission, such that D. citri transmission of CLas is more efficient when bacteria are acquired by nymphs when compared with adults. We hypothesize that expression changes in the D. citri immune system and commensal microbiota occur during development and regulate vector competency. In support of this hypothesis, more proteins, with greater fold changes, were differentially expressed in response to CLas in adults when compared with nymphs, including insect proteins involved in bacterial adhesion and immunity. Compared with nymphs, adult insects had a higher titre of CLas and the bacterial endosymbionts Wolbachia, Profftella and Carsonella. All Wolbachia and Profftella proteins differentially expressed between nymphs and adults are upregulated in adults, while most differentially expressed Carsonella proteins are upregulated in nymphs. Discovery of protein interaction networks has broad applicability to the study of host–microbe relationships. Using protein interaction reporter technology, a D. citri haemocyanin protein highly upregulated in response to CLas was found to physically interact with the CLas coenzyme A (CoA) biosynthesis enzyme phosphopantothenoylcysteine synthetase/decarboxylase. CLas pantothenate kinase, which catalyses the rate-limiting step of CoA biosynthesis, was found to interact with a D. citri myosin protein. Two Carsonella enzymes involved in histidine and tryptophan biosynthesis were found to physically interact with D. citri proteins. These co-evolved protein interaction networks at the host–microbe interface are highly specific targets for controlling the insect vector responsible for the spread of citrus greening.
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spelling pubmed-53672802017-04-06 Protein interaction networks at the host–microbe interface in Diaphorina citri, the insect vector of the citrus greening pathogen Ramsey, J. S. Chavez, J. D. Johnson, R. Hosseinzadeh, S. Mahoney, J. E. Mohr, J. P. Robison, F. Zhong, X. Hall, D. G. MacCoss, M. Bruce, J. Cilia, M. R Soc Open Sci Cellular and Molecular Biology The Asian citrus psyllid (Diaphorina citri) is the insect vector responsible for the worldwide spread of ‘Candidatus Liberibacter asiaticus’ (CLas), the bacterial pathogen associated with citrus greening disease. Developmental changes in the insect vector impact pathogen transmission, such that D. citri transmission of CLas is more efficient when bacteria are acquired by nymphs when compared with adults. We hypothesize that expression changes in the D. citri immune system and commensal microbiota occur during development and regulate vector competency. In support of this hypothesis, more proteins, with greater fold changes, were differentially expressed in response to CLas in adults when compared with nymphs, including insect proteins involved in bacterial adhesion and immunity. Compared with nymphs, adult insects had a higher titre of CLas and the bacterial endosymbionts Wolbachia, Profftella and Carsonella. All Wolbachia and Profftella proteins differentially expressed between nymphs and adults are upregulated in adults, while most differentially expressed Carsonella proteins are upregulated in nymphs. Discovery of protein interaction networks has broad applicability to the study of host–microbe relationships. Using protein interaction reporter technology, a D. citri haemocyanin protein highly upregulated in response to CLas was found to physically interact with the CLas coenzyme A (CoA) biosynthesis enzyme phosphopantothenoylcysteine synthetase/decarboxylase. CLas pantothenate kinase, which catalyses the rate-limiting step of CoA biosynthesis, was found to interact with a D. citri myosin protein. Two Carsonella enzymes involved in histidine and tryptophan biosynthesis were found to physically interact with D. citri proteins. These co-evolved protein interaction networks at the host–microbe interface are highly specific targets for controlling the insect vector responsible for the spread of citrus greening. The Royal Society Publishing 2017-02-08 /pmc/articles/PMC5367280/ /pubmed/28386418 http://dx.doi.org/10.1098/rsos.160545 Text en © 2017 The Authors. http://creativecommons.org/licenses/by/4.0/ Published by the Royal Society under the terms of the Creative Commons Attribution License http://creativecommons.org/licenses/by/4.0/, which permits unrestricted use, provided the original author and source are credited.
spellingShingle Cellular and Molecular Biology
Ramsey, J. S.
Chavez, J. D.
Johnson, R.
Hosseinzadeh, S.
Mahoney, J. E.
Mohr, J. P.
Robison, F.
Zhong, X.
Hall, D. G.
MacCoss, M.
Bruce, J.
Cilia, M.
Protein interaction networks at the host–microbe interface in Diaphorina citri, the insect vector of the citrus greening pathogen
title Protein interaction networks at the host–microbe interface in Diaphorina citri, the insect vector of the citrus greening pathogen
title_full Protein interaction networks at the host–microbe interface in Diaphorina citri, the insect vector of the citrus greening pathogen
title_fullStr Protein interaction networks at the host–microbe interface in Diaphorina citri, the insect vector of the citrus greening pathogen
title_full_unstemmed Protein interaction networks at the host–microbe interface in Diaphorina citri, the insect vector of the citrus greening pathogen
title_short Protein interaction networks at the host–microbe interface in Diaphorina citri, the insect vector of the citrus greening pathogen
title_sort protein interaction networks at the host–microbe interface in diaphorina citri, the insect vector of the citrus greening pathogen
topic Cellular and Molecular Biology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5367280/
https://www.ncbi.nlm.nih.gov/pubmed/28386418
http://dx.doi.org/10.1098/rsos.160545
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