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Murine scent mark microbial communities are genetically determined

Lookup NU author(s): Dr Clare Lanyon, Professor Stephen Rushton, Professor Anthony O'Donnell, Professor Michael Goodfellow, Emeritus Professor Alan Ward, Dr Susanne Jensen, Emeritus Professor Morris Gosling


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Scent marking in mice allows males to communicate information such as territory ownership, male competitive ability and current reproductive, nutritional, social and health status. It has been suggested that female mice eavesdrop on these olfactory cues, using them as a means of selecting mates with dissimilar major histocompatibility complex (MHC) genes, known as H2 in mice. The mechanisms underpinning MHC-dependent olfactory communication remain unresolved. Using congenic mouse strains and molecular methods we explore the involvement of the microbial communities, a known source of odourants, in scent marks to test the hypothesis that the microbial communities and hence the olfactory signals are genetically determined. Here we show that the indigenous microbial community of murine scent marks is genetically determined. Both background genotype and H2 haplotype influence the community structure of the scent mark flora, removing the possibility that community composition is solely orchestrated by the MHC. Qualitative and quantitative components of the bacterial community associated with MHC haplotype and background genotype were identified. The analyses confirm that the four groups of congenic mice tested are distinguishable on basis of the microbiology of their scent marks alone, strengthening the role of microorganisms in the development of MHC-dependent odours. © 2006 Federation of European Microbiological Societies.

Publication metadata

Author(s): Lanyon CV, Rushton SP, O'Donnell AG, Goodfellow M, Ward AC, Petrie M, Jensen SP, Gosling LM, Penn DJ

Publication type: Article

Publication status: Published

Journal: FEMS Microbiology Ecology

Year: 2007

Volume: 59

Issue: 3

Pages: 576-583

Print publication date: 01/03/2007

ISSN (print): 0168-6496

ISSN (electronic): 1574-6941

Publisher: Wiley-Blackwell


DOI: 10.1111/j.1574-6941.2006.00252.x

PubMed id: 17381516


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