Mycolic acid modification by the mmaA4 gene of M. tuberculosis modulates IL-12 production

DN Dao, K Sweeney, T Hsu, Sudagar Gurcha, IP Nascimento, D Roshevsky, Gurdyal Besra, J Chan, SA Porcelli, WR Jacobs

Research output: Contribution to journalArticle

80 Citations (Scopus)

Abstract

Mycobacterium tuberculosis has evolved many strategies to evade elimination by the host immune system, including the selective repression of macrophage IL-12p40 production. To identify the M. tuberculosis genes responsible for this aspect of immune evasion, we used a macrophage cell line expressing a reporter for IL-12p40 transcription to screen a transposon library of M. tuberculosis for mutants that lacked this function. This approach led to the identification of the mmaA4 gene, which encodes a methyl transferase required for introducing the distal oxygen-containing modifications of mycolic acids, as a key locus involved in the repression of IL-12p40. Mutants in which mmaA4 (hma) was inactivated stimulated macrophages to produce significantly more IL-12p40 and TNF-alpha than wild-type M. tuberculosis and were attenuated for virulence. This attenuation was not seen in IL-12p40-deficient mice, consistent with a direct linkage between enhanced stimulation of IL-12p40 by the mutant and its reduced virulence. Treatment of macrophages with trehalose dimycolate (TDM) purified from the Delta mmaA4 mutant stimulated increased IL-12p40, similar to the increase observed from DmmaA4 mutant-infected macrophages. In contrast, purified TDM isolated from wild-type M. tuberculosis inhibited production of IL-12p40 by macrophages. These findings strongly suggest that M. tuberculosis has evolved mmaA4-derived mycolic acids, including those incorporated into TDM to manipulate IL-12-mediated immunity and virulence.
Original languageEnglish
Pages (from-to)e1000081
JournalPLoS pathogens
Volume4
Issue number6
DOIs
Publication statusPublished - 1 Jun 2008

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