Mapping leprosy-associated coding variants of interleukin genes by targeted sequencing

Previous genotyping-based assays have identified non-coding variants of several interleukins (ILs) being associated with genetic susceptibility to leprosy. However, understanding of the involvement of coding variants within all IL family genes in leprosy was still limited. To obtain the full mutation spectrum of all ILs in leprosy, we performed a targeted deep sequencing of coding regions of 58 ILs genes in 798 leprosy patients (age 56.2 +/- 14.4; female 31.5%) and 990 healthy controls (age 38.1 +/- 14.0; female 44.3%) from Yunnan, Southwest China. mRNA expression alterations of ILs in leprosy skin lesions or in response to M. leprae treatment were estimated by using publicly available expression datasets. Two coding variants in IL27 (rs17855750, p.S59A, p = 4.02 x 10(-8), odds ratio [OR] = 1.748) and IL1RN (rs45507693, p.A106T, p = 1.45 x 10(-5), OR = 3.629) were significantly associated with leprosy risk. mRNA levels of IL27 and IL1RN were upregulated in whole blood cells after M. leprae stimulation. These data showed that IL27 and IL1RN are leprosy risk genes. Further functional study is required for characterizing the exact role of ILs in leprosy.

Automated summary

Deep sequencing of IL genes in leprosy patients and healthy controls revealed two coding variants in IL27 and IL1RN significantly associated with leprosy risk. Upregulation of IL27 and IL1RN mRNA levels in whole blood cells after M.leprae stimulation suggests their potential role in leprosy pathogenesis.