Waruhiu Cecilia, Ommeh Sheila, Obanda Vincent, Agwanda Bernard, Gakuya Francis, Ge Xing-Yi, Yang Xing-Lou, Wu Li-Jun, Zohaib Ali, Hu Ben, Shi Zheng-Li
Key Lab of Special Pathogens, Wuhan Institute of Virology, Chinese Academy of Sciences, Wuhan, 430071, China.
Sino-Africa Joint Research Center, Chinese Academy of Sciences, Wuhan, 430071, China.
Virol Sin. 2017 Apr;32(2):101-114. doi: 10.1007/s12250-016-3930-2. Epub 2017 Apr 6.
This is the first country-wide surveillance of bat-borne viruses in Kenya spanning from 2012-2015 covering sites perceived to have medium to high level bat-human interaction. The objective of this surveillance study was to apply a non-invasive approach using fresh feces to detect viruses circulating within the diverse species of Kenyan bats. We screened for both DNA and RNA viruses; specifically, astroviruses (AstVs), adenoviruses (ADVs), caliciviruses (CalVs), coronaviruses (CoVs), flaviviruses, filoviruses, paramyxoviruses (PMVs), polyomaviruses (PYVs) and rotaviruses. We used family-specific primers, amplicon sequencing and further characterization by phylogenetic analysis. Except for filoviruses, eight virus families were detected with varying distributions and positive rates across the five regions (former provinces) studied. AstVs (12.83%), CoVs (3.97%), PMV (2.4%), ADV (2.26%), PYV (1.65%), CalVs (0.29%), rotavirus (0.19%) and flavivirus (0.19%). Novel CalVs were detected in Rousettus aegyptiacus and Mops condylurus while novel Rotavirus-A-related viruses were detected in Taphozous bats and R. aegyptiacus. The two Rotavirus A (RVA) strains detected were highly related to human strains with VP6 genotypes I2 and I16. Genotype I16 has previously been assigned to human RVA-strain B10 from Kenya only, which raises public health concern, particularly considering increased human-bat interaction. Additionally, 229E-like bat CoVs were detected in samples originating from Hipposideros bats roosting in sites with high human activity. Our findings confirm the presence of diverse viruses in Kenyan bats while providing extended knowledge on bat virus distribution. The detection of viruses highly related to human strains and hence of public health concern, underscores the importance of continuous surveillance.
这是2012年至2015年期间在肯尼亚首次开展的全国范围内对蝙蝠传播病毒的监测,监测地点涵盖了被认为蝙蝠与人类有中到高水平接触的区域。这项监测研究的目的是采用一种非侵入性方法,利用新鲜粪便检测肯尼亚不同种类蝙蝠体内传播的病毒。我们对DNA病毒和RNA病毒都进行了筛查;具体包括星状病毒(AstVs)、腺病毒(ADVs)、杯状病毒(CalVs)、冠状病毒(CoVs)、黄病毒、丝状病毒、副粘病毒(PMVs)、多瘤病毒(PYVs)和轮状病毒。我们使用了家族特异性引物、扩增子测序,并通过系统发育分析进行进一步表征。除丝状病毒外,在研究的五个地区(原省份)检测到了八个病毒家族,其分布和阳性率各不相同。星状病毒(12.83%)、冠状病毒(3.97%)、副粘病毒(2.4%)、腺病毒(2.26%)、多瘤病毒(1.65%)、杯状病毒(0.29%)、轮状病毒(0.19%)和黄病毒(0.19%)。在埃及果蝠和髭蝠中检测到了新型杯状病毒,而在鞘尾蝠和埃及果蝠中检测到了新型轮状病毒A相关病毒。检测到的两种轮状病毒A(RVA)毒株与人类毒株高度相关,VP6基因型分别为I2和I16。基因型I16此前仅被指定为来自肯尼亚的人类RVA毒株B10,这引发了公共卫生方面的担忧,特别是考虑到人类与蝙蝠的接触增加。此外,在来自栖息于人类活动频繁地区的蹄蝠样本中检测到了229E样蝙蝠冠状病毒。我们的研究结果证实了肯尼亚蝙蝠中存在多种病毒,同时提供了关于蝙蝠病毒分布的更多知识。检测到与人类毒株高度相关且因此涉及公共卫生问题的病毒,凸显了持续监测的重要性。