Wielders C C H, Hackert V H, Schimmer B, Hodemaekers H M, de Klerk A, Hoebe C J P A, Schneeberger P M, van Duynhoven Y T H P, Janssen R
Department of Medical Microbiology and Infection Control, Jeroen Bosch Hospital, P.O. Box 90153, 5200 ME, 's-Hertogenbosch, The Netherlands,
Eur J Clin Microbiol Infect Dis. 2015 May;34(5):943-50. doi: 10.1007/s10096-014-2310-9. Epub 2015 Jan 11.
Genes involved in human immune response are well recognized to influence the clinical course of infection. The association of host genetics with susceptibility to and severity of clinical symptoms in acute Q fever was investigated. Single nucleotide polymorphisms (SNPs) in the IFNG (rs2430561/rs1861493), STAT1 (rs1914408), and VDR (rs2228570) genes were determined in 85 patients from the 2007 Dutch acute Q fever outbreak, and a symptom score was calculated. IFNG rs1861493 showed a significant association with the symptom score; IFNG rs2430561 showed a similar trend. These SNPs were then used to reproduce results in a 2009 outbreak population (n = 123). The median symptom score differed significantly in both populations: 2 versus 7. The significant association of IFNG rs1861493 with symptom score in the first population was not reproduced in the second population. We hypothesize that individuals in the second outbreak were exposed to a higher Coxiella burnetii dose compared to the first, which overruled the protection conferred by the A-allele of IFNG rs1861493 in the first population.
人们已经充分认识到,参与人类免疫反应的基因会影响感染的临床病程。本研究调查了宿主遗传学与急性Q热临床症状易感性及严重程度之间的关联。对2007年荷兰急性Q热疫情中的85名患者,测定了IFNG(rs2430561/rs1861493)、STAT1(rs1914408)和VDR(rs2228570)基因的单核苷酸多态性(SNP),并计算症状评分。IFNG rs1861493与症状评分显著相关;IFNG rs2430561呈现类似趋势。随后,利用这些SNP在2009年疫情人群(n = 123)中重现结果。两个群体的症状评分中位数差异显著:分别为2和7。IFNG rs1861493与第一个群体症状评分的显著关联在第二个群体中未得到重现。我们推测,与第一个群体相比,第二个疫情中的个体接触到的伯氏考克斯氏体剂量更高,这抵消了IFNG rs1861493的A等位基因在第一个群体中提供的保护作用。