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Symbcompat

Determing symbiont factors that affect compatibility with a novel host

Total Cost €

0

EC-Contrib. €

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Partnership

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Project "Symbcompat" data sheet

The following table provides information about the project.

Coordinator
THE UNIVERSITY OF LIVERPOOL 

Organization address
address: BROWNLOW HILL 765 FOUNDATION BUILDING
city: LIVERPOOL
postcode: L69 7ZX
website: www.liverpool.ac.uk

contact info
title: n.a.
name: n.a.
surname: n.a.
function: n.a.
email: n.a.
telephone: n.a.
fax: n.a.

 Coordinator Country United Kingdom [UK]
 Project website https://sites.google.com/site/hurstlab/home/lab-members
 Total cost 183˙454 €
 EC max contribution 183˙454 € (100%)
 Programme 1. H2020-EU.1.3.2. (Nurturing excellence by means of cross-border and cross-sector mobility)
 Code Call H2020-MSCA-IF-2015
 Funding Scheme MSCA-IF-EF-ST
 Starting year 2016
 Duration (year-month-day) from 2016-10-01   to  2018-09-30

 Partnership

Take a look of project's partnership.

# participants  country  role  EC contrib. [€] 
1    THE UNIVERSITY OF LIVERPOOL UK (LIVERPOOL) coordinator 183˙454.00

Map

 Project objective

Symbiosis between multicellular organisms and microbial symbionts is near universal, and it is now clear that many aspects of organismal biology in health and disease cannot be understood without reference to interactions with microbes. In insects, this includes a diverse range of heritable symbionts, which pass from a female host to her progeny. These symbionts are highly adapted to their host, and encode important properties, such as defence against natural enemies. In contrast to classical adaptive phenotypes, symbiont traits generally arise through a host shift event – the movement of a microbe from into a novel host species. Experimental host shift experiments indicate that there is a compatibility filter: some symbionts in novel host species cause little pathology and transmit vertically efficiently, whereas other do not. Understanding this compatibility filter will clarify the patterns through which host shifts occur in nature, and create a principled basis for manipulation of compatibility, for instance in symbiont-mediated control of vector competence. In this proposal, the causes of poor symbiont-host compatibility will be established for the first time. We will first examine what symbiont/host systems malfunction in a poorly performing symbiosis, examining whether phage lysis or illegitimate toxin production affect symbiont titre and virulence in the novel host. We will then determine the genetic basis of symbiont compatibility using a novel experimental evolution approach. Symbiont compatibility is known to increase on passage in novel hosts, and the proposal will use comparative genomics of evolved vs ancestral symbionts to establish the loci that are subject to selection during the evolution of compatibility. The results of this project will impact both upon our understanding of an important natural process and enable better exploitation of symbiont encoded traits in control of vector born disease.

 Publications

year authors and title journal last update
List of publications.
2018 Stefanos Siozios, Michael Gerth, Joanne S. Griffin, Gregory D.D. Hurst
Symbiosis: Wolbachia Host Shifts in the Fast Lane
published pages: R269-R271, ISSN: 0960-9822, DOI: 10.1016/j.cub.2018.02.008
Current Biology 28/6 2019-05-13
2017 Michael Gerth, Gregory D.D. Hurst
Short reads from honey bee ( Apis sp.) sequencing projects reflect microbial associate diversity
published pages: e3529, ISSN: 2167-8359, DOI: 10.7717/peerj.3529
PeerJ 5 2019-05-13

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