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Mol Ecol. 2016 Mar;25(6):1324-39. doi: 10.1111/mec.13558.

The mammalian complement system as an epitome of host-pathogen genetic conflicts.

Author information

1
Bioinformatics, Scientific Institute IRCCS E. MEDEA, 23842, Bosisio Parini, Italy.
2
Department of Biotechnology and Biosciences, University of Milan-Bicocca, 20126, Milan, Italy.
3
Dino Ferrari Centre, Department of Physiopathology and Transplantation, University of Milan, Fondazione Ca' Granda IRCCS Ospedale Maggiore Policlinico, 20122, Milan, Italy.
4
Department of Physiopathology and Transplantation, University of Milan, 20090, Milan, Italy.
5
Don C. Gnocchi Foundation ONLUS, IRCCS, 20148, Milan, Italy.

Abstract

The complement system is an innate immunity effector mechanism; its action is antagonized by a wide array of pathogens and complement evasion determines the virulence of several infections. We investigated the evolutionary history of the complement system and of bacterial-encoded complement-interacting proteins. Complement components targeted by several pathogens evolved under strong selective pressure in primates, with selection acting on residues at the contact interface with microbial/viral proteins. Positively selected sites in CFH and C4BPA account for the human specificity of gonococcal infection. Bacterial interactors, evolved adaptively as well, with selected sites located at interaction surfaces with primate complement proteins. These results epitomize the expectation under a genetic conflict scenario whereby the host's and the pathogen's genes evolve within binding avoidance-binding seeking dynamics. In silico mutagenesis and protein-protein docking analyses supported this by showing that positively selected sites, both in the host's and in the pathogen's interacting partner, modulate binding.

KEYWORDS:

complement system; host-pathogen genetic conflict; human-specific infections; positive selection

PMID:
26836579
DOI:
10.1111/mec.13558
[Indexed for MEDLINE]

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