Department of Pediatrics, All India Institute of Medical Sciences, New Delhi, India.
PLoS One. 2012;7(2):e30025. doi: 10.1371/journal.pone.0030025. Epub 2012 Feb 17.
Chikungunya (CHIKV) has recently seen a re-emergence in India with high morbidity. However, the epidemiology and disease burden remain largely undetermined. A prospective multi-centric study was conducted to evaluate clinical, epidemiological and virological features of chikugunya infection in patients with acute febrile illness from various geographical regions of India.
A total of 540 patients with fever of up to 7 days duration were enrolled at Karnataka Institute of Medical Sciences (KIMS), Karnataka (South); Sawai Man Singh Medical College (SMS) Rajasthan (West), and All India Institute of Medical Sciences (AIIMS) New Delhi (North) from June 2008 to May 2009. Serum specimens were screened for chikungunya infection concurrently through RT-PCR and serology (IgM). Phylogenetic analysis was performed using Bioedit and Mega2 programs. Chikungunya infection was detected in 25.37% patients by RT-PCR and/or IgM-ELISA. Highest cases were detected in south (49.36%) followed by west (16.28%) and north (0.56%) India. A difference in proportion of positives by RT-PCR/ELISA with regard to duration of fever was observed (p<0.05). Rashes, joint pain/swelling, abdominal pain and vomiting was frequently observed among chikungunya confirmed cases (p<0.05). Adults were affected more than children. Anti-CHIK antibodies (IgM) were detected for more than 60 days of fever onset. Phylogenetic analysis based on E1 gene from KIMS patients (n = 15) revealed ∼99% homology clustering with Central/East African genotype. An amino acid change from lysine to glutamine at position 132 of E1 gene was frequently observed among strains infecting children.
The study documented re-emergence of chikungunya in high frequencies and severe morbidity in south and west India but rare in north. The study emphasizes the need for continuous surveillance for disease burden using multiple diagnostic tests and also warrants the need for an appropriate molecular diagnostic for early detection of chikungunya virus.
基孔肯雅热(CHIKV)在印度再次出现,发病率很高。然而,其流行病学和疾病负担在很大程度上仍未确定。本前瞻性多中心研究旨在评估来自印度不同地理区域的急性发热性疾病患者中基孔肯雅热感染的临床、流行病学和病毒学特征。
2008 年 6 月至 2009 年 5 月,在卡纳塔克邦的 Karnataka Institute of Medical Sciences(KIMS)、拉贾斯坦邦的 Sawai Man Singh Medical College(SMS)和新德里的 All India Institute of Medical Sciences(AIIMS)共纳入了 540 名发热时间不超过 7 天的患者。通过 RT-PCR 和血清学(IgM)同时筛查血清标本是否存在基孔肯雅热感染。使用 Bioedit 和 Mega2 程序进行系统发育分析。通过 RT-PCR 和/或 IgM-ELISA 在 25.37%的患者中检测到基孔肯雅热感染。南部(49.36%)的病例最多,其次是西部(16.28%)和北部(0.56%)印度。观察到发热时间长短与 RT-PCR/ELISA 阳性率之间存在差异(p<0.05)。在确诊的基孔肯雅热病例中,皮疹、关节痛/肿胀、腹痛和呕吐较为常见(p<0.05)。成人比儿童更易受感染。在发热超过 60 天的患者中检测到抗-CHIK 抗体(IgM)。基于来自 KIMS 患者的 E1 基因的系统发育分析(n=15)显示,与中非/东非基因型的同源性聚类约为 99%。在感染儿童的病毒株中,E1 基因第 132 位的赖氨酸经常发生到谷氨酰胺的氨基酸变化。
本研究记录了基孔肯雅热在印度南部和西部高频率和严重发病,但在北部很少见。该研究强调需要使用多种诊断试验持续监测疾病负担,也需要适当的分子诊断方法来早期检测基孔肯雅病毒。