Yeo Dawn Su-Yin, Lian Jing Er, Fernandez Charlene J, Lin Yueh-Nuo, Liaw Jasper Chin-Wen, Soh Moi-Lien, Lim Elizabeth Ai-Sim, Chan Kwai-Peng, Ng Mah-Lee, Tan Hwee-Cheng, Oh Serena, Ooi Eng-Eong, Tan Boon-Huan
Virol J. 2013 Aug 2;10:248. doi: 10.1186/1743-422X-10-248.
In 2001 and 2002, fatal myocarditis resulted in the sudden deaths of four, two adult and two juvenile, orang utans out of a cohort of 26 in the Singapore Zoological Gardens.
Of the four orang utans that underwent post-mortem examination, virus isolation was performed from the tissue homogenates of the heart and lung obtained from the two juvenile orang utans in Vero cell cultures. The tissue culture fluid was examined using electron microscopy. Reverse transcription and polymerase chain reaction with Encephalomyocarditis virus (EMCV)-specific primers targeting the gene regions of VP3/VP1 and 3D polymerase (3Dpol) confirmed the virus genus and species. The two EMCV isolates were sequenced and phylogenetic analyses of the virus genes performed. Serological testing on other animal species in the Singapore Zoological Gardens was also conducted.
Electron microscopy of the two EMCV isolates, designated Sing-M100-02 and Sing-M105-02, revealed spherical viral particles of about 20 to 30 nm, consistent with the size and morphology of members belonging to the family Picornaviridae. In addition, infected-Vero cells showed positive immunoflorescence staining with antiserum to EMCV. Sequencing of the viral genome showed that the two EMCV isolates were 99.9% identical at the nucleotide level, indicating a similar source of origin. When compared with existing EMCV sequences in the VP1 and 3Dpol gene regions, the nucleotide divergence were at a maximum of 38.8% and 23.6% respectively, while the amino acid divergence were at a maximum of 33.9% and 11.3% respectively. Phylogenetic analyses of VP1 and 3Dpol genes further grouped the Sing-M100-02 and Sing-M105-02 isolates to themselves, away from existing EMCV lineages. This strongly suggested that Sing-M100-02 and Sing-M105-02 isolates are highly divergent variants of EMCV. Apart from the two deceased orang utans, a serological survey conducted among other zoo animals showed that a number of other animal species had neutralizing antibodies to Sing-M105-02 isolate, indicating that the EMCV variant has a relatively wide host range.
The etiological agent responsible for the fatal myocarditis cases among two of the four orang utans in the Singapore Zoological Gardens was a highly divergent variant of EMCV. This is the first report of an EMCV infection in Singapore and South East Asia.
2001年和2002年,新加坡动物园26只猩猩中有4只突然死亡,其中2只为成年猩猩,2只为幼年猩猩,死因是致命性心肌炎。
对4只进行了尸检的猩猩,从两只幼年猩猩的心脏和肺组织匀浆中提取病毒,接种于非洲绿猴肾细胞(Vero细胞)进行病毒分离培养。对细胞培养液进行电子显微镜检查。采用针对脑心肌炎病毒(EMCV)VP3/VP1基因区域和3D聚合酶(3Dpol)基因区域的特异性引物进行逆转录聚合酶链反应,以确定病毒的属和种。对分离得到的两株EMCV进行测序,并对病毒基因进行系统发育分析。同时对新加坡动物园的其他动物进行血清学检测。
对两株分别命名为Sing-M100-02和Sing-M105-02的EMCV进行电子显微镜检查,发现病毒粒子呈球形,直径约20至30纳米,与小RNA病毒科成员的大小和形态一致。此外,感染EMCV的Vero细胞用抗EMCV血清进行免疫荧光染色呈阳性。病毒基因组测序结果显示,两株EMCV在核苷酸水平上的同源性为99.9%,表明它们来源相似。与现有的EMCV在VP1和3Dpol基因区域的序列相比,核苷酸差异分别最大为38.8%和23.6%,氨基酸差异分别最大为33.9%和11.3%。对VP1和3Dpol基因的系统发育分析进一步表明,Sing-M100-02和Sing-M105-02分离株自成一簇,与现有的EMCV谱系不同。这强烈提示Sing-M100-02和Sing-M105-02分离株是EMCV的高度变异株。除了两只死亡的猩猩外,对其他动物园动物进行的血清学调查显示,许多其他动物物种对Sing-M105-02分离株具有中和抗体,表明该EMCV变异株具有相对广泛的宿主范围。
新加坡动物园4只猩猩中2只因致命性心肌炎死亡的病原体是EMCV的高度变异株。这是新加坡和东南亚地区首次报告EMCV感染。