The mammalian cell entry (Mce) protein of pathogenic Leptospira species is responsible for RGD motif-dependent infection of cells and animals

ORCiD

David M. Ojcius: 0000-0003-1461-4495

Department

Biomedical Sciences

Document Type

Article

Publication Title

Molecular Microbiology

ISSN

0950-382X

Volume

83

Issue

5

DOI

10.1111/j.1365-2958.2012.07985.x

First Page

1006

Last Page

1023

Publication Date

3-1-2012

Abstract

Mammalian cell entry proteins (Mces) contribute to Mycobacterium tuberculosis virulence. A mce homologue has been identified in the Leptospira interrogans genome, but its function was unknown. We showed that the mce gene is expressed only by pathogenic Leptospira strains tested. Leptospiral mce mRNA and Mce protein levels increased during infection of macrophages. The ability to infect macrophages was significantly lower in a strain with the mce gene deleted (mce-). Complementation of the mce gene restored the ability of the mutant strain (mcecom) to adhere to and invade cells. Importantly, the mce gene knock-in strain (mce+) derived from L. biflexa acquired the ability to infect cells, and the mce+/ΔRAA knock-in strain (in which the RGD motif was replaced by RAA) was unable to infect cells. The mce- mutant was also dramatically less efficient in infecting hamsters than the wild-type L. interrogans strain, and fewer leptospires of the mutant were found in peripheral blood monocytes and the urine from infected animals. The recombinant Mce protein showed a high binding affinity to the integrins α5β1 and αVβ3. Blockade of the two integrins or the Mce protein decreased leptospiral adherence and invasiveness. The results showed that Mce is an RGD-motif-dependent virulence factor in pathogenic Leptospira species.

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