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Citation: Marakalala MJ, Ndlovu H (2017) Signaling C-type lectin receptors in antimycobacterial immunity. PLoS Pathog 13(6): e1006333. Editor: John M. Leong, Tufts Univ School of Medicine, UNITED STATES Published: June 22, 2017 Copyright: © 2017 Marakalala, Ndlovu. This is an open access article distributed under the terms of the, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. Funding: The authors acknowledge funding from the South African Medical Research Council (SAMRC) self-initiated research grant () (MJM), The National Research Foundation () (MJM), SAMRC with funding from South African Department of Health (), and the University of Cape Town (HN and MJM). The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.

We acknowledge Dr. Claire Hoving for useful discussions. Competing interests: The authors have declared that no competing interests exist. Introduction The mammalian innate immune system is composed of phagocytes such as macrophages and dendritic cells that serve as the first line of defense against microbial infections. Tomtom map meta keygens download for windows.

These cells express various pattern recognition receptors (PRRs) that recognize specific pathogen-associated molecular patterns (PAMPs) on the surface of or inside microorganisms []. PRRs such as Toll-like receptors (TLRs), C-type lectin receptors (CLRs), and Nucleotide-binding Oligomerization Domain (NOD)-like receptors (NLRs) have been widely studied in antimicrobial immunity and homeostasis. These PRRs have also been implicated in antimycobacterial immunity, with CLRs recently receiving considerable attention. CLRs are a large family of proteins containing at least 1 carbohydrate-recognition domain (CRD) that in most cases binds a range of carbohydrate-based PAMPs, including trehalose 6,6’ dimycolate (TDM), lipoarabinomannan (LAM), lipomannan (LM), and phosphatidylinositol mannosides (PIMs) [–].