Iwashita Hanako, Higa Yukiko, Futami Kyoko, Lutiali Peter A, Njenga Sammy M, Nabeshima Takeshi, Minakawa Noboru
1Department of Vector Ecology and Environment, Institute of Tropical Medicine, Nagasaki University, 1-12-4 Sakamoto, Nagasaki, 852-8523 Japan.
2Department of Bacteriology, Graduate School of Medicine, University of the Ryukyus, 207 Uehara, Nishiharacho, Okinawa, 903-0125 Japan.
Trop Med Health. 2018 Jun 4;46:19. doi: 10.1186/s41182-018-0095-8. eCollection 2018.
Many arboviral outbreaks have occurred in various locations in Kenya. Entomological surveys are suitable methods for revealing information about circulating arboviruses before human outbreaks are recognized. Therefore, mosquitoes were collected in Kenya to determine the distribution of arboviruses.
Various species of mosquitoes were sampled from January to July 2012 using several collection methods. Mosquito homogenates were directly tested by reverse transcription-polymerase chain reaction (RT-PCR) using various arbovirus-targeted primer pairs.
We collected 12,569 mosquitoes. Although no human-related arboviruses were detected, Culex flavivirus (CxFV), an insect-specific arbovirus, was detected in 54 pools of 324 individuals collected during the rainy season. Of these 54 positive pools, 96.3% (52/54) of the mosquitoes were collected in Busia, on the border of western Kenya and Uganda. The remaining two CxFV-positive pools were collected in Mombasa and Kakamega, far from Busia. Phylogenetic analysis revealed minimal genetic diversity among the CxFVs collected in Mombasa, Kakamega, and Busia, even though these cities are in geographically different regions. Additionally, CxFV was detected in one mosquito pool collected in Mombasa during the dry season. In addition to mosquitoes, () and mosquitoes were also positive for the genus. Cell fusing agent virus was detected in one pool of . Mosquito flavivirus was detected in three pools of s.l collected in the dry and rainy seasons.
Although no mosquitoes were positive for human-related arbovirus, insect-specific viruses were detected in various species of mosquitoes. The heterogeneity observed in the number of CxFVs in mosquitoes in different locations in Kenya suggests that the abundance of human-related viruses might differ depending on the abundance of insect-specific viruses. We may have underestimated the circulation of any human-related arbovirus in Kenya, and the collection of larger samples may allow for determination of the presence of human-related arboviruses.
肯尼亚多个地区发生了许多虫媒病毒疫情。在人类疫情被发现之前,昆虫学调查是揭示有关传播虫媒病毒信息的合适方法。因此,在肯尼亚采集蚊子以确定虫媒病毒的分布。
2012年1月至7月,使用多种采集方法对不同种类的蚊子进行采样。蚊子匀浆通过逆转录聚合酶链反应(RT-PCR),使用各种针对虫媒病毒的引物对直接进行检测。
我们共采集了12,569只蚊子。虽然未检测到与人类相关的虫媒病毒,但在雨季采集的324只个体的54组样本中检测到了一种昆虫特异性虫媒病毒——库蚊黄病毒(CxFV)。在这54个阳性样本组中,96.3%(52/54)的蚊子是在肯尼亚西部与乌干达接壤的布西亚采集的。其余两个CxFV阳性样本组是在远离布西亚的蒙巴萨和卡卡梅加采集的。系统发育分析表明,尽管蒙巴萨、卡卡梅加和布西亚位于不同的地理区域,但在这些地方采集的CxFV之间的遗传多样性极小。此外,在旱季于蒙巴萨采集的一组蚊子样本中也检测到了CxFV。除了蚊子,(此处原文缺失信息)和(此处原文缺失信息)蚊子对(此处原文缺失信息)属也呈阳性。在一组(此处原文缺失信息)中检测到了细胞融合剂病毒。在旱季和雨季采集的三组(此处原文缺失信息)s.l样本中检测到了蚊黄病毒。
虽然没有蚊子对与人类相关的虫媒病毒呈阳性,但在不同种类的蚊子中检测到了昆虫特异性病毒。在肯尼亚不同地点的(此处原文缺失信息)蚊子中观察到的CxFV数量的异质性表明,与人类相关的病毒的丰度可能因昆虫特异性病毒的丰度而异。我们可能低估了肯尼亚任何与人类相关的虫媒病毒的传播情况,采集更大的样本可能有助于确定与人类相关的虫媒病毒的存在。