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Grant: Discovery Grants Program - Individual

University of Western Ontario

$40,000.00

Molecular analyses of the iron starvation response in the coagulase-negative group of staphylococci

FY 2014-15

Summary
Iron is required by all life forms, yet it's very low availability frequently make it a growth-limiting nutrient. This presents significant problems to all life forms which must therefore find innovative ways to gain access to this nutrient in order to survive. This is no less true for bacteria. Many bacteria emit what are called siderophores into the surrounding environment to bind iron and deliver iron back to the bacterial cell. Many bacteria that are found in association with humans and animals can also capture iron out of hemoglobin as a way to support their own survival. A group of bacteria called coagulase-negative staphylococci are typically referred to as commensals, that is, they live in close association with animals and humans and do not cause disease but rather promote health. Indeed, experts estimate that there are actually 10 times as many bacteria found in and on mammals than there are mammalian cells. For coagulase-negative staphylococci, their very presence on skin and mucous membranes actually helps defend against infection by disease-causing bacteria. This research will identify the ways in which these bacteria access iron as a means to survive and and grow. With our NSERC-funded history of characterizing iron acquisition systems in the highly infectious Staph aureus bacterium, the research to be undertaken on the commensal bacteria over the next five years will provide us with a fundamental understanding of similarities and differences in iron acquisition systems in major disease-causing bacteria versus important commensal bacteria that are much less likely to cause infection. This research will inform us about the possibilities of whether antibacterials that might target iron acquisition processes in the disease-causing bacteria will have collateral effects on commensal bacteria.
Program
Discovery Grants Program - Individual
Location
Ontario, Canada
Recipient Type
Academia
Type
Grant
Source
NSERC's Awards Data

As published

Application id
227295-2011
Name nom
Heinrichs, David
Department département
Microbiology and Immunology
Organization id
36
Institution établissement
University of Western Ontario
Province en
Ontario
Province fr
Ontario
Country en
CANADA
Country fr
CANADA
Fiscal year exercice financier
2014
Competition year année de concours
2011
Award amount
40000
Program id
RGPIN
Program name en
Discovery Grants Program - Individual
Program name fr
Programme de subventions à la découverte - individuelles
Group en
Discovery grants programs
Group fr
Programmes de subventions à la découverte
Committee code
1501
Committee name en
Genes, Cells and Molecules
Committee name fr
Gènes, cellules et molécules
Area of application code
1200
Area of application group en
Advancement of knowledge
Area of application group fr
Avancement des connaissances
Area of application en
Advancement of knowledge
Area of application fr
Avancement des connaissances
Research subject code
5201
Research subject group en
Microbiology
Research subject group fr
Microbiologie
Research subject en
Bacteriology
Research subject fr
Bactériologie
Partie
4
Nb partie
5
Application title
Molecular analyses of the iron starvation response in the coagulase-negative group of staphylococci
Keyword
NSERC
Application summary
Iron is required by all life forms, yet it's very low availability frequently make it a growth-limiting nutrient. This presents significant problems to all life forms which must therefore find innovative ways to gain access to this nutrient in order to survive. This is no less true for bacteria. Many bacteria emit what are called siderophores into the surrounding environment to bind iron and deliver iron back to the bacterial cell. Many bacteria that are found in association with humans and animals can also capture iron out of hemoglobin as a way to support their own survival. A group of bacteria called coagulase-negative staphylococci are typically referred to as commensals, that is, they live in close association with animals and humans and do not cause disease but rather promote health. Indeed, experts estimate that there are actually 10 times as many bacteria found in and on mammals than there are mammalian cells. For coagulase-negative staphylococci, their very presence on skin and mucous membranes actually helps defend against infection by disease-causing bacteria. This research will identify the ways in which these bacteria access iron as a means to survive and and grow. With our NSERC-funded history of characterizing iron acquisition systems in the highly infectious Staph aureus bacterium, the research to be undertaken on the commensal bacteria over the next five years will provide us with a fundamental understanding of similarities and differences in iron acquisition systems in major disease-causing bacteria versus important commensal bacteria that are much less likely to cause infection. This research will inform us about the possibilities of whether antibacterials that might target iron acquisition processes in the disease-causing bacteria will have collateral effects on commensal bacteria.