1928年在肯尼亚发现的内脏利什曼病传播媒介Phlebotomus(Artemievus)alexandri Sinton表明了复杂的传播动力学

IF 1.7 Q3 PARASITOLOGY
Steve Kiplagat , Jandouwe Villinger , Collins K. Kigen , Kevin O. Kidambasi , Jackson M. Muema , Stephie M. Mwangi , Maureen Wangari , Damaris Matoke-Muhia , Daniel K. Masiga , Joel L. Bargul
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引用次数: 0

摘要

内脏和皮肤利什曼病是特定地区的地方病,这是由于抽血沙蝇和利什曼原虫的生态偏好。传播。由于对利什曼病的研究有限和忽视,肯尼亚北部的沙蝇昆虫学数据很少。本研究的目的是调查:(i)沙蝇的多样性和分布;(ii)在沙蝇体内出现利什曼原虫DNA;以及(iii)肯尼亚北部莱萨米斯的沙蝇血粉来源。2021年2月和3月,我们使用美国疾病控制与预防中心的标准光阱在莱萨米斯县的五个地区进行了昆虫学调查。共鉴定了1009只沙蝇(394只雄性和615只雌性),并通过细胞色素c氧化酶亚基1(cox1)基因的PCR扩增和测序验证了代表性样本。同样,我们通过脊椎动物细胞色素b(cyt b)基因和28S rRNA基因的内部转录间隔区1(ITS1)的PCR扩增子测序,分别鉴定了雌性沙蝇的血粉来源和利什曼原虫DNA。沙蝇种群数量最多(59.8%)。尽管主要从一个地方(蒂加莫)采集,14.8%的样本属于Phlebotomus(Artemievus)alexandri Sinton,1928年。在亚历山大假单胞菌(Ph.alexandri)中检出主要利什曼原虫(Leishmania major)DNA的比例为5.19%,而在克氏假单胞菌中检出主要利什曼原虫DNA的比例分别为7.51%、8.00%和8.33%。亚历山大假单胞菌和克莱迪假单胞菌都主要以人类为食,可能参与皮肤利什曼病的传播。这项研究的发现有助于了解沙蝇媒介种群及其在该地区传播利什曼病的潜力。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Discovery of the vector of visceral leishmaniasis, Phlebotomus (Artemievus) alexandri Sinton, 1928, in Kenya suggests complex transmission dynamics

Discovery of the vector of visceral leishmaniasis, Phlebotomus (Artemievus) alexandri Sinton, 1928, in Kenya suggests complex transmission dynamics

Visceral and cutaneous leishmaniasis are endemic to specific regions due to the ecological preferences of phlebotomine sand flies and Leishmania spp. transmission. Sand fly entomological data in northern Kenya are scarce due to limited studies and neglect of leishmaniasis. The aim of this study was to investigate: (i) sand fly diversity and distribution; (ii) occurrence of Leishmania DNA within sand flies; and (iii) blood-meal sources of sand flies in Laisamis, northern Kenya. We conducted an entomological survey during February and March of 2021 in five areas of Laisamis sub-county using standard CDC light traps. A total of 1009 sand flies (394 male and 615 female) were morphologically identified, and representative samples verified by PCR amplification and sequencing of the cytochrome c oxidase subunit 1 (cox1) gene. Similarly, we identified blood-meal sources and Leishmania DNA in female sand flies by PCR amplicon sequencing of the vertebrate cytochrome b (cyt b) gene and internal transcribed spacer 1 (ITS1) of the 28S rRNA gene, respectively. Sergentomyia clydei (59.8%) was the most abundant sand fly species. Though collected mainly from one locality (Tirgamo), 14.8% of samples belonged to Phlebotomus (Artemievus) alexandri Sinton, 1928. We detected DNA of Leishmania major in 5.19% of Ph. alexandri, whereas Leishmania adleri DNA was detected in S. clydei (7.51%), Sergentomyia squamipleuris (8.00%), and Sergentomyia africanus (8.33%). Nine of 13 blood-fed sand flies had obtained blood from humans, of which 33.3% had L. major DNA. Both Ph. alexandri and S. clydei primarily fed on humans and could potentially be involved in the transmission of cutaneous leishmaniasis. The findings of this study contribute to the understanding of sand fly vector populations and their potential to transmit leishmaniasis in the area.

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