Genetics of the switch from predatory to axenic growth in the living antibiotic Bdellovibrio bacteriovorus
Genetics of the switch from predatory to axenic growth in the living antibiotic Bdellovibrio bacteriovorus
批准号:
BB/G013632/1
负责人:
Renee Sockett
金额:
$49.06万
依托单位:
依托单位国家:
英国
项目类别:
Research Grant
财政年份:
2009
资助国家:
英国
项目状态:
已结题
起止时间:
2009 至 --
中文摘要
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英文摘要
Bdellovibrio are small, human-friendly, predatory bacteria which invade the cells of other pathogenic bacteria (such as ones that give old people infections in pressure sores and diabetic ulcers, and bacteria that infect crop plants) and kill them. Bdellovibrio have no activities against human, animal or plant cells but they are naturally good at killing other bacteria. Pathogenic bacteria do not have simple cell surface receptors for Bdellovibrio attachment and invasion and so it is not easy for them to develop resistance to the Bdellovibrio (unlike the situation with conventional antibiotics) Bdellovibrio were discovered in the 1960s and recently we and others have been researching their genes and genomes and trying to understand how they may be useful to humans. We propose that they can be used in a cream or a spray to apply to infected wounds in humans and also to be sprayed on infected crop plants to kill off infections crop rot bacteria. Bdellovibrio are almost unique in being predatory bacteria, most bacteria grow on foods and do not invade live bacteria. Bdellovibrio actually have a large 3.8Mb genome (which we helped to sequence in 2004) and have got both the genes to grow like normal bacteria, and the genes to be predatory.To be efficient at killing pathogens Bdellovibrio will have to lose the ability to grow normally on food like regular bacteria, because that ability allows them to grow in serum in wounds and in sap and on soil around plants, without needing to be predatory and kill the target pathogenic bacteria that are causing the infection. So, the point of our project is to work out how they grow non-predatorily (as so-called HI strains), we will work out which genes code for these properties and try to inactivate them, without impairing predatory growth (which we want to use to kill the pathogens). Previous scientists have published one nice paper in 1992 showing that one gene, in a region of the genome called the hit locus, has changes within it when the Bdellovibrio are growing non predatorily as HIs and that this might be partly responsible, but another paper in 2001 showed that not all Bdellovibrio that were growing non-predatorily had changes in this locus, so there are more important genes to find in the process too. No-one has yet found out what the hit locus gene does and how it might control HI growth- we want to do this here and to see how genetically stable HI strains may be if we produce as living antibiotics. We have carried out previous research that has shown all the genes switched on from the genome when the Bdellovibrio are growing predatorily and when they are growing as HIs; there are lots of gene differences and some are specifically switched on just to grow as HIs. We want to investigate what these genes do, especially some that regulate the switching on of groups of genes- we may be able to delete one of these regulator genes and switch off the whole HI growing abilities, leaving an obligately predatory Bdellovibrio for use as a living antibiotic. We have also already been able to isolate a mutant Bdellovibrio by chance, that we found to be unable to grow as an HI and which is therefore obligately predatory. This strain has a defect in obtaining iron for growth from complex molecules, yet can grow fine in the predatory growth mode, probably because it is able to free the iron from prey bacteria by digesting their proteins. Thus this strain shows that we will be able to knock out genes in Bdellovibrio that control HI growth without abolishing the ability to grow predatorily. In our project we want to profile the genes that are expressed in our iron-scavenging mutant that can't grow as an HI, to try to understand what is wrong with it. The long term idea is to develop Bdellovibrio as a real new treatment for human, animal and plant disease and this is one of the important first steps
期刊论文(8)
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DOI:
10.1128/mbio.00163-11
发表时间:
2011
期刊:
mBio
影响因子:
6.4
作者:
[Lovering AL, Capeness MJ, Lambert C, Hobley L, Sockett RE]
通讯作者:
Sockett RE
DOI:
10.1371/journal.pone.0079759
发表时间:
2013
期刊:
PloS one
影响因子:
3.7
作者:
[Capeness MJ, Lambert C, Lovering AL, Till R, Uchida K, Chaudhuri R, Alderwick LJ, Lee DJ, Swarbreck D, Liddell S, Aizawa S, Sockett RE]
通讯作者:
Sockett RE
DOI:
10.1371/journal.pone.0094403
发表时间:
2014
期刊:
PloS one
影响因子:
3.7
作者:
[Gruninger RJ, Thibault J, Capeness MJ, Till R, Mosimann SC, Sockett RE, Selinger BL, Lovering AL]
通讯作者:
Lovering AL
DOI:
10.1186/1471-2164-13-670
发表时间:
2012-11-27
期刊:
BMC genomics
影响因子:
4.4
作者:
[Hobley L, Lerner TR, Williams LE, Lambert C, Till R, Milner DS, Basford SM, Capeness MJ, Fenton AK, Atterbury RJ, Harris MA, Sockett RE]
通讯作者:
Sockett RE
DOI:
10.1371/journal.ppat.1002493
发表时间:
2012-02
期刊:
PLoS pathogens
影响因子:
6.7
作者:
[Hobley L, Fung RK, Lambert C, Harris MA, Dabhi JM, King SS, Basford SM, Uchida K, Till R, Ahmad R, Aizawa S, Gomelsky M, Sockett RE]
通讯作者:
Sockett RE
共 6 条
The Bacterial Invasion Port of Bdellovibrio
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批准号:BB/M010325/1
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项目类别:Research Grant
-
资助金额:$52.75万
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财政年份:2015
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负责人:Renee Sockett
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依托单位:
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项目类别:Research Grant
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资助金额:$66.98万
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财政年份:2008
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负责人:Renee Sockett
-
依托单位:
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