Literature DB >> 31126937

Effects of Exposure Time and Biological State on Acquisition and Accumulation of Erwinia amylovora by Drosophila melanogaster.

Matthew Boucher1, Rowan Collins2, Kerik Cox3, Greg Loeb4.   

Abstract

Fire blight, caused by the bacterium Erwinia amylovora, is a disease devastating the production of rosaceous crops, primarily apple and pear, with worldwide distribution. Fire blight begins in the spring when primary inoculum is produced as ooze, which consists of plant sap, E. amylovora, and exopolysaccharides. Ooze is believed to be transferred to healthy tissues by wind, rain, and insects. However, the mechanisms by which insects locate and transmit ooze are largely undocumented. The goals of this study were to investigate the biological factors affecting acquisition of E. amylovora from ooze by a model dipteran, Drosophila melanogaster, and to determine whether flies are able to mechanically transfer this bacterium after acquisition. We found that the percentage of positive flies increased as exposure time increased, but nutritional state, mating status, and sex did not significantly alter the number of positive individuals. Bacterial abundance was highly variable at all exposure times, suggesting that other biological factors play a role in acquisition. Nutritional state had a significant effect on E. amylovora abundance, and food-deprived flies had higher E. amylovora counts than satiated flies. We also demonstrated that D. melanogaster transmits E. amylovora to a selective medium surface and hypothesize that the same is possible for plant surfaces, where bacteria can persist until an opportunity to colonize the host arises. Collectively, these data suggest a more significant role for flies than previously thought in transmission of fire blight and contribute to a shift in our understanding of the E. amylovora disease cycle.IMPORTANCE A recent hypothesis proposed that dissemination of Erwinia amylovora from ooze by flies to native rosaceous trees was likely key to the life cycle of the bacterium during its evolution. Our study validates an important component of this hypothesis by showing that flies are capable of acquiring and transmitting this bacterium from ooze under various biotic conditions. Understanding how dipterans interact with ooze advances our current knowledge of its epidemiological function and provides strong evidence for an underappreciated role of flies in the disease cycle. These findings may be especially important as they pertain to shoot blight, because this stage of the disease is poorly understood and may involve a significant amount of insect activity. Broadly, this study underscores a need to consider the depth, breadth, and origin of interactions between flies and E. amylovora to better understand its epidemiology.
Copyright © 2019 American Society for Microbiology.

Entities:  

Keywords:  Diptera; fire blight; insect-microbe interactions; plant disease epidemiology

Mesh:

Year:  2019        PMID: 31126937      PMCID: PMC6643243          DOI: 10.1128/AEM.00726-19

Source DB:  PubMed          Journal:  Appl Environ Microbiol        ISSN: 0099-2240            Impact factor:   4.792


  23 in total

Review 1.  Type III secretion machines: bacterial devices for protein delivery into host cells.

Authors:  J E Galán; A Collmer
Journal:  Science       Date:  1999-05-21       Impact factor: 47.728

2.  Complete genome sequence of the plant pathogen Erwinia amylovora strain ATCC 49946.

Authors:  M Sebaihia; A M Bocsanczy; B S Biehl; M A Quail; N T Perna; J D Glasner; G A DeClerck; S Cartinhour; D J Schneider; S D Bentley; J Parkhill; S V Beer
Journal:  J Bacteriol       Date:  2010-01-29       Impact factor: 3.490

Review 3.  Molecular genetics of Erwinia amylovora involved in the development of fire blight.

Authors:  Chang-Sik Oh; Steven V Beer
Journal:  FEMS Microbiol Lett       Date:  2005-10-13       Impact factor: 2.742

4.  Prandiology of Drosophila and the CAFE assay.

Authors:  William W Ja; Gil B Carvalho; Elizabeth M Mak; Noelle N de la Rosa; Annie Y Fang; Jonathan C Liong; Ted Brummel; Seymour Benzer
Journal:  Proc Natl Acad Sci U S A       Date:  2007-05-09       Impact factor: 11.205

5.  HrpN of Erwinia amylovora functions in the translocation of DspA/E into plant cells.

Authors:  Ana M Bocsanczy; Riitta M Nissinen; Chang-Sik Oh; Steven V Beer
Journal:  Mol Plant Pathol       Date:  2008-07       Impact factor: 5.663

6.  Construction and analysis of pathogenicity island deletion mutants of Erwinia amylovora.

Authors:  Youfu Zhao; George W Sundin; Dongping Wang
Journal:  Can J Microbiol       Date:  2009-04       Impact factor: 2.419

7.  Contribution of Erwinia amylovora exopolysaccharides amylovoran and levan to biofilm formation: implications in pathogenicity.

Authors:  Jessica M Koczan; Molly J McGrath; Youfu Zhao; George W Sundin
Journal:  Phytopathology       Date:  2009-11       Impact factor: 4.025

8.  The phytopathogen Dickeya dadantii (Erwinia chrysanthemi 3937) is a pathogen of the pea aphid.

Authors:  Anne-Marie Grenier; Gabrielle Duport; Sylvie Pagès; Guy Condemine; Yvan Rahbé
Journal:  Appl Environ Microbiol       Date:  2006-03       Impact factor: 4.792

9.  Host-Specific Phytotoxic Polysaccharide from Apple Tissue Infected by Erwinia amylovora.

Authors:  R N Goodman; J S Huang; P Y Huang
Journal:  Science       Date:  1974-03-15       Impact factor: 47.728

10.  The phytopathogenic bacteria Erwinia carotovora infects Drosophila and activates an immune response.

Authors:  A Basset; R S Khush; A Braun; L Gardan; F Boccard; J A Hoffmann; B Lemaitre
Journal:  Proc Natl Acad Sci U S A       Date:  2000-03-28       Impact factor: 11.205

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