Modification of the mycobacteriophage Ms6 attP core allows the integration of multiple vectors into different tRNAala T-loops in slow- and fast-growing mycobacteria | Research - Institut Pasteur

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Cross-reactivity studies of an anti-Plasmodium vivax apical membrane antigen 1 monoclonal antibody: binding and structural characterisation

Candida albicans outbreak in a neurosurgical intensive care unit

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Published in BMC molecular biology - 15 Dec 2006

Vultos TD, Méderlé I, Abadie V, Pimentel M, Moniz-Pereira J, Gicquel B, Reyrat JM, Winter N

Link to Pubmed [PMID] – 17173678

BMC Mol. Biol. 2006;7:47

Mycobacteriophage Ms6 integrates into Mycobacterium smegmatis and M. bovis BCG chromosome at the 3′ end of tRNAala genes. Homologous recombination occurs between the phage attP core and the attB site located in the T-loop. Integration-proficient vectors derived from Ms6 are useful genetic tools, but their insertion sites in the BCG chromosome remain poorly defined. The primary objective of this study was to identify Ms6 target genes in M. smegmatis and BCG. We then aimed to modify the attP site in Ms6-derived vectors, to switch integration to other tRNAala loci. This provided the basis for the development of recombinant M. bovis BCG strains expressing several reporter genes inserted into different tRNAala genes.

Published on: 15 Dec 2006