Mahapatra Dharitri, Sarangi Gitanjali, Mahapatra Ashoka, Paty Bimoch Projna, Das Padma, Chayani Nirupama
Assistant Professor, Department of Microbiology, S.C.B Medical College , Cuttack, Odisha, India .
Associate Professor, Department of Microbiology, S.C.B Medical College , Cuttack, Odisha, India .
J Clin Diagn Res. 2014 Aug;8(8):DC08-10. doi: 10.7860/JCDR/2014/8589.4697. Epub 2014 Aug 20.
An outbreak of dengue infection occurred in Angul district of Odisha in the month of August & September, 2011. The study was undertaken to detect NS1 antigen positivity among the study population, to compare IgM capture ELISA with NS1 antigen detection for diagnosis of dengue and to identify the predominant genotype of Dengue virus responsible for the outbreak.
Total 1020 serum samples were collected from clinically suspected cases of dengue from the outbreak. All were subjected for NS1 antigen detection, 92 were selected based on their clinical severity of illness (fever, rash, bleeding manifestation, arthralgia) for further study of IgM ELISA and platelet count and 148 NS1 positive samples were selected from different Blocks of Anugul district for RT-PCR at NIV, Pune, India.
Five hundred and thirteen (50.2%) samples were positive for NS1 antigen (highly significant p-value <0.0001, C.I - 95%) with 88% positivity during 1-5 days. The NS1 Ag positivity was peaked to 86.9% on days 3 to 5 (Sensitivity & NPV - 100% each) & declined to 6.2% during 6-10 days with a low sensitivity of 7.14% but 100% specificity & PPV. However, the IgM antibody positivity was 81.2% on days 6 to 10 and 87.5% after 10 days (Sensitivity- 100%, Specificity-13.33%,PPV-7.14% & NPV - 100%). RT-PCR resulted 32.4% positivity (6- DEN1, 39 - DEN 2 & 3- DEN 3) among which 20% were in IgM +ve & 68% in IgM -ve cases.
Therefore, early diagnosis of dengue could be mainly by NS1 antigen detection whereas Ig M ELISA is a better tool during the later stage of infection &RT-PCR is more effective in IgM -ve cases.The predominant genotype responsible for the outbreak was found to be DEN-2.
2011年8月和9月,印度奥里萨邦安古尔地区爆发登革热感染疫情。开展本研究旨在检测研究人群中NS1抗原的阳性情况,比较IgM捕获ELISA法与NS1抗原检测法在登革热诊断中的效果,并确定引发此次疫情的登革热病毒的主要基因型。
从疫情中临床疑似登革热病例中总共采集了1020份血清样本。所有样本均进行NS1抗原检测,根据疾病临床严重程度(发热、皮疹、出血表现、关节痛)从其中选取92份样本进一步进行IgM ELISA检测和血小板计数,从安古尔地区不同街区选取148份NS1阳性样本送往印度浦那的国家病毒研究所进行RT-PCR检测。
513份(50.2%)样本NS1抗原呈阳性(p值高度显著<0.0001,95%置信区间),在第1至5天阳性率为88%。NS1抗原阳性率在第3至5天达到峰值86.9%(敏感性和阴性预测值均为100%),在第6至10天降至6.2%,敏感性低至7.14%,但特异性和阳性预测值为100%。然而,IgM抗体阳性率在第6至10天为81.2%,10天后为87.5%(敏感性-100%,特异性-13.33%,阳性预测值-7.14%,阴性预测值-100%)。RT-PCR检测阳性率为32.4%(6份为DEN1型,39份为DEN2型,3份为DEN3型),其中IgM阳性病例中占20%,IgM阴性病例中占68%。
因此,登革热的早期诊断主要依靠NS1抗原检测,而IgM ELISA在感染后期是更好的检测工具,RT-PCR在IgM阴性病例中更有效。发现引发此次疫情的主要基因型为DEN-2型。