Bedoukian   RussellIPM   RussellIPM   Piezoelectric Micro-Sprayer


Home
Animal Taxa
Plant Taxa
Semiochemicals
Floral Compounds
Semiochemical Detail
Semiochemicals & Taxa
Synthesis
Control
Invasive spp.
References

Abstract

Guide

Alphascents
Pherobio
InsectScience
E-Econex
Counterpart-Semiochemicals
Print
Email to a Friend
Kindly Donate for The Pherobase

« Previous AbstractNitrogen utilization and biomass yield in trickle bed air biofilters    Next AbstractDevelopment of air-blast dried non-Saccharomyces yeast starter for improving quality of Korean persimmon wine and apple cider »

PLoS One


Title:Behavioral interplay between mosquito and mycolactone produced by Mycobacterium ulcerans and bacterial gene expression induced by mosquito proximity
Author(s):Kim D; Crippen TL; Dhungel L; Delclos PJ; Tomberlin JK; Jordan HR;
Address:"Department of Entomology, Texas A&M University, College Station, Texas, United States of America. Southern Plains Agricultural Research Center, Agricultural Research Service, USDA, College Station, Texas, United States of America. Department of Biological Sciences, Mississippi State University, Starkville, Mississippi, United States of America. Department of Natural Sciences, University of Houston-Downtown, Houston, Texas, United States of America"
Journal Title:PLoS One
Year:2023
Volume:20230803
Issue:8
Page Number:e0289768 -
DOI: 10.1371/journal.pone.0289768
ISSN/ISBN:1932-6203 (Electronic) 1932-6203 (Linking)
Abstract:"Mycolactone is a cytotoxic lipid metabolite produced by Mycobacterium ulcerans, the environmental pathogen responsible for Buruli ulcer, a neglected tropical disease. Mycobacterium ulcerans is prevalent in West Africa, particularly found in lentic environments, where mosquitoes also occur. Researchers hypothesize mosquitoes could serve as a transmission mechanism resulting in infection by M. ulcerans when mosquitoes pierce skin contaminated with M. ulcerans. The interplay between the pathogen, mycolactone, and mosquito is only just beginning to be explored. A triple-choice assay was conducted to determine the host-seeking preference of Aedes aegypti between M. ulcerans wildtype (MU, mycolactone active) and mutant (MUlac-, mycolactone inactive). Both qualitative and quantitative differences in volatile organic compounds' (VOCs) profiles of MU and MUlac- were determined by GC-MS. Additionally, we evaluated the interplay between Ae. aegypti proximity and M. ulcerans mRNA expression. The results showed that mosquito attraction was significantly greater (126.0%) to an artificial host treated with MU than MUlac-. We found that MU and MUlac produced differential profiles of VOCs associated with a wide range of biological importance from quorum sensing (QS) to human odor components. RT-qPCR assays showed that mycolactone upregulation was 24-fold greater for MU exposed to Ae. aegypti in direct proximity. Transcriptome data indicated significant induction of ten chromosomal genes of MU involved in stress responses and membrane protein, compared to MUlac- when directly having access to or in near mosquito proximity. Our study provides evidence of possible interkingdom interactions between unicellular and multicellular species that MU present on human skin is capable of interreacting with unrelated species (i.e., mosquitoes), altering its gene expression when mosquitoes are in direct contact or proximity, potentially impacting the production of its VOCs, and consequently leading to the stronger attraction of mosquitoes toward human hosts. This study elucidates interkingdom interactions between viable M. ulcerans bacteria and Ae. aegypti mosquitoes, which rarely have been explored in the past. Our finding opens new doors for future research in terms of disease ecology, prevalence, and pathogen dispersal outside of the M. ulcerans system"
Keywords:Animals Humans *Mycobacterium ulcerans/genetics *Buruli Ulcer/microbiology Macrolides/metabolism *Aedes/physiology Gene Expression;
Notes:"MedlineKim, Dongmin Crippen, Tawni L Dhungel, Laxmi Delclos, Pablo J Tomberlin, Jeffery K Jordan, Heather R eng Research Support, Non-U.S. Gov't 2023/08/03 PLoS One. 2023 Aug 3; 18(8):e0289768. doi: 10.1371/journal.pone.0289768. eCollection 2023"

 
Back to top
 
Citation: El-Sayed AM 2024. The Pherobase: Database of Pheromones and Semiochemicals. <http://www.pherobase.com>.
© 2003-2024 The Pherobase - Extensive Database of Pheromones and Semiochemicals. Ashraf M. El-Sayed.
Page created on 05-12-2024