Vanithamani Shanmugam, Shanmughapriya Santhanam, Narayanan Ramasamy, Raja Veerapandian, Kanagavel Murugesan, Sivasankari Karikalacholan, Natarajaseenivasan Kalimuthusamy
Medical Microbiology Laboratory, Department of Microbiology, Centre of Excellence in Life Sciences, Bharathidasan University, Tiruchirappalli, 620 024, India.
PLoS One. 2015 Sep 4;10(9):e0137130. doi: 10.1371/journal.pone.0137130. eCollection 2015.
Leptospirosis is a re-emerging infectious disease that is under-recognized due to low-sensitivity and cumbersome serological tests. MAT is the gold standard test and it is the only serogroup specific test used till date. Rapid reliable alternative serogroup specific tests are needed for surveillance studies to identify locally circulating serogroups in the study area.
METHODS/PRINCIPAL FINDINGS: In the present investigation the serological specificity of leptospiral lipopolysaccharides (LPS) was evaluated by enzyme linked immunosorbent assay (ELISA), dot blot assay and rapid immunochromatography based lateral flow assay (ICG-LFA). Sera samples from 120 MAT positive cases, 174 cases with febrile illness other than leptospirosis, and 121 seronegative healthy controls were evaluated for the diagnostic sensitivity and specificity of the developed assays. LPS was extracted from five locally predominant circulating serogroups including: Australis (27.5%), Autumnalis (11.7%), Ballum (25.8%), Grippotyphosa (12.5%), Pomona (10%) and were used as antigens in the diagnostics to detect IgM antibodies in patients' sera. The sensitivity observed by IgM ELISA and dot blot assay using various leptospiral LPS was >90% for homologous sera. Except for Ballum LPS, no other LPS showed cross-reactivity to heterologous sera. An attempt was made to develop LPS based ICG-LFA for rapid and sensitive serogroup specific diagnostics of leptospirosis. The developed ICG-LFA showed sensitivity in the range between 93 and 100% for homologous sera. The Wilcoxon analysis showed LPS based ICG-LFA did not differ significantly from the gold standard MAT (P>0.05).
The application of single array of LPS for serogroup specific diagnosis is first of its kind. The developed assay could potentially be evaluated and employed for as MAT alternative.
钩端螺旋体病是一种再度出现的传染病,由于血清学检测灵敏度低且操作繁琐,其未得到充分认识。显微凝集试验(MAT)是金标准检测方法,也是迄今为止唯一使用的血清群特异性检测方法。监测研究需要快速可靠的替代血清群特异性检测方法,以识别研究区域内本地流行的血清群。
方法/主要发现:在本研究中,通过酶联免疫吸附测定(ELISA)、斑点印迹法和基于快速免疫层析的侧向流动分析(ICG-LFA)评估了钩端螺旋体脂多糖(LPS)的血清学特异性。对120例MAT阳性病例、174例非钩端螺旋体病的发热性疾病病例和121例血清阴性的健康对照的血清样本进行检测,以评估所开发检测方法的诊断敏感性和特异性。从五个本地主要流行的血清群中提取LPS,包括:澳洲型(27.5%)、秋季型(11.7%)、拜伦型(25.8%)、犬型(12.5%)、波摩那型(10%),并将其用作诊断抗原,以检测患者血清中的IgM抗体。使用各种钩端螺旋体LPS的IgM ELISA和斑点印迹法对同源血清的敏感性>90%。除拜伦型LPS外,没有其他LPS对异源血清显示交叉反应。尝试开发基于LPS的ICG-LFA,用于钩端螺旋体病的快速、敏感血清群特异性诊断。所开发的ICG-LFA对同源血清的敏感性在93%至100%之间。威尔科克森分析表明,基于LPS的ICG-LFA与金标准MAT无显著差异(P>0.05)。
单一LPS阵列用于血清群特异性诊断的应用尚属首次。所开发的检测方法有可能作为MAT的替代方法进行评估和应用。