| Literature DB >> 27535927 |
Lauren Forbes-Beadle1, Tova Crossman2, Travis K Johnson1, Richard Burke2, Coral G Warr3, James C Whisstock4.
Abstract
Pore-forming members of the membrane attack complex/perforin-like (MACPF) protein superfamily perform well-characterized roles as mammalian immune effectors. For example, complement component 9 and perforin function to directly form pores in the membrane of Gram-negative pathogens or virally infected/transformed cells, respectively. In contrast, the only known MACPF protein in Drosophila melanogaster, Torso-like, plays crucial roles during development in embryo patterning and larval growth. Here, we report that in addition to these functions, Torso-like plays an important role in Drosophila immunity. However, in contrast to a hypothesized effector function in, for example, elimination of Gram-negative pathogens, we find that torso-like null mutants instead show increased susceptibility to certain Gram-positive pathogens such as Staphylococcus aureus and Enterococcus faecalis We further show that this deficit is due to a severely reduced number of circulating immune cells and, as a consequence, an impaired ability to phagocytose bacterial particles. Together these data suggest that Torso-like plays an important role in controlling the development of the Drosophila cellular immune system.Entities:
Keywords: Drosophila melanogaster; Torso-like; cellular immunity; genetics of immunity; membrane attack complex/perforin-like proteins; phagocytosis
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Year: 2016 PMID: 27535927 PMCID: PMC5068854 DOI: 10.1534/genetics.115.185462
Source DB: PubMed Journal: Genetics ISSN: 0016-6731 Impact factor: 4.562