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. Author manuscript; available in PMC: 2014 Oct 1.
Published in final edited form as: J Immunol. 2014 Aug 27;193(7):3704–3716. doi: 10.4049/jimmunol.1401018

TABLE 1. Distribution across clinically relevant microbial pathogens of key biosynthetic pathways that produce metabolites targeted by human unconventional T cells.

Non-mevalonate pathway
(Vγ9/Vδ2 T cell activation)
Vitamin B2 synthesis
(MAIT cell activation)
Gram-negative bacteria
Acinetobacter baumannii + +
Chryseobacterium gleum +
Enterobacter cloacae + +
Escherichia coli + +
Haemophilus influenzae + +
Helicobacter pylori + +
Klebsiella pneumoniae + +
Legionella pneumophila +
Neisseria meningitidis + +
Pseudomonas aeruginosa + +
Shigella dysenteriae + +

Gram-positive bacteria
Bacillus anthracis + +
Clostridium difficile + +
Corynebacterium diphtheriae + +
Enterococcus faecalis
Listeria monocytogenes +
Mycobacterium tuberculosis + +
Propionibacterium acnes + +
Staphylococcus aureus +
Streptococcus pyogenes

Other bacteria
Borrelia burgdorferi
Leptospira interrogans + +
Mycoplasma genitalium
Mycoplasma penetrans +
Treponema pallidum

Yeasts, fungi
Aspergillus fumigatus +
Candida albicans +
Crytococcus neoformans +
Saccharomyces cerevisiae +