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1.
PLoS One ; 15(10): e0239771, 2020.
Article in English | MEDLINE | ID: mdl-33022020

ABSTRACT

Huanglongbing (HLB) is a deadly, incurable citrus disease putatively caused by the unculturable bacterium, 'Candidatus Liberibacter asiaticus' (CLas), and transmitted by Diaphorina citri. Prior studies suggest D. citri transmits CLas in a circulative and propagative manner; however, the precise interactions necessary for CLas transmission remain unknown, and the impact of insect sex on D. citri-CLas interactions is poorly understood despite reports of sex-dependent susceptibilities to CLas. We analyzed the transcriptome, proteome, metabolome, and microbiome of male and female adult D. citri reared on healthy or CLas-infected Citrus medica to determine shared and sex-specific responses of D. citri and its endosymbionts to CLas exposure. More sex-specific than shared D. citri responses to CLas were observed, despite there being no difference between males and females in CLas density or relative abundance. CLas exposure altered the abundance of proteins involved in immunity and cellular and oxidative stress in a sex-dependent manner. CLas exposure impacted cuticular proteins and enzymes involved in chitin degradation, as well as energy metabolism and abundance of the endosymbiont 'Candidatus Profftella armatura' in both sexes similarly. Notably, diaphorin, a toxic Profftella-derived metabolite, was more abundant in both sexes with CLas exposure. The responses reported here resulted from a combination of CLas colonization of D. citri as well as the effect of CLas infection on C. medica. Elucidating these impacts on D. citri and their endosymbionts contributes to our understanding of the HLB pathosystem and identifies the responses potentially critical to limiting or promoting CLas acquisition and propagation in both sexes.


Subject(s)
Citrus/microbiology , Hemiptera/microbiology , Insect Vectors/microbiology , Plant Diseases/microbiology , Rhizobiaceae/physiology , Rhizobiaceae/pathogenicity , Symbiosis/physiology , Animals , Citrus/metabolism , Citrus/physiology , Female , Hemiptera/metabolism , Hemiptera/physiology , Insect Vectors/metabolism , Insect Vectors/physiology , Male , Metabolome/physiology , Microbiota/physiology , Oxidative Stress/physiology , Proteome/metabolism , Transcriptome/physiology
2.
PLoS One ; 12(6): e0179531, 2017.
Article in English | MEDLINE | ID: mdl-28632769

ABSTRACT

Huanglongbing, or citrus greening disease, is an economically devastating bacterial disease of citrus. It is associated with infection by the gram-negative bacterium Candidatus Liberibacter asiaticus (CLas). CLas is transmitted by Diaphorina citri, the Asian citrus psyllid (ACP). For insect transmission to occur, CLas must be ingested during feeding on infected phloem sap and cross the gut barrier to gain entry into the insect vector. To investigate the effects of CLas exposure at the gut-pathogen interface, we performed RNAseq and mass spectrometry-based proteomics to analyze the transcriptome and proteome, respectively, of ACP gut tissue. CLas exposure resulted in changes in pathways involving the TCA cycle, iron metabolism, insecticide resistance and the insect's immune system. We identified 83 long non-coding RNAs that are responsive to CLas, two of which appear to be specific to the ACP. Proteomics analysis also enabled us to determine that Wolbachia, a symbiont of the ACP, undergoes proteome regulation when CLas is present. Fluorescent in situ hybridization (FISH) confirmed that Wolbachia and CLas inhabit the same ACP gut cells, but do not co-localize within those cells. Wolbachia cells are prevalent throughout the gut epithelial cell cytoplasm, and Wolbachia titer is more variable in the guts of CLas exposed insects. CLas is detected on the luminal membrane, in puncta within the gut epithelial cell cytoplasm, along actin filaments in the gut visceral muscles, and rarely, in association with gut cell nuclei. Our study provides a snapshot of how the psyllid gut copes with CLas exposure and provides information on pathways and proteins for targeted disruption of CLas-vector interactions at the gut interface.


Subject(s)
Hemiptera/microbiology , Proteome/analysis , Proteomics , Rhizobiaceae/physiology , Transcriptome , Animals , Apoptosis/genetics , Citric Acid Cycle/genetics , Citrus/microbiology , Digestive System/metabolism , Digestive System/microbiology , Down-Regulation , Hemiptera/genetics , Insect Vectors/microbiology , Microscopy, Confocal , Mitochondria/metabolism , Plant Diseases/microbiology , RNA/chemistry , RNA/isolation & purification , RNA/metabolism , Sequence Analysis, RNA , Up-Regulation
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