台湾地区血革螨(蜱螨目:革螨科)中吉氏巴贝斯虫经卵传递的分子证据:犬巴贝斯虫的新型传播媒介。

Molecular evidence for the transovarial passage of Babesia gibsoni in Haemaphysalis hystricis (Acari: Ixodidae) ticks from Taiwan: a novel vector for canine babesiosis.

机构信息

Utrecht Centre for Tick-borne Diseases (UCTD), FAO Reference Centre for Ticks and Tick-borne Diseases, Faculty of Veterinary Medicine, Utrecht University, Yalelaan 1, 3584, CL, Utrecht, The Netherlands.

Vectors and Vector-borne Diseases Research Programme, Department of Veterinary Tropical Diseases, Faculty of Veterinary Science, University of Pretoria, Private Bag X04, Onderstepoort, 0110, South Africa.

出版信息

Parasit Vectors. 2018 Mar 20;11(1):134. doi: 10.1186/s13071-018-2722-y.

Abstract

BACKGROUND

Babesia gibsoni is the predominant tick-borne protozoan blood parasite affecting dogs throughout the Oriental region. Babesia gibsoni is transmitted by Haemaphysalis longicornis, whereas a similar role has been suggested for Rhipicephalus sanguineus. Haemaphysalis longicornis does not occur in Taiwan, but R. sanguineus is widely distributed on dogs. However, clinical cases of babesiosis are mainly restricted to the northern part of the island. The discrepancy between tick distribution and clinical cases stimulated us to investigate the tick species distribution on dogs in northern Taiwan, with the aim to identify the local vector for canine babesiosis.

METHODS

Ticks were collected from stray dogs or free ranging pet dogs in northern Taiwan between 2015 and 2017 and, after identification, were tested for the presence of tick-borne Babesia parasites using PCR and reverse line blot (RLB) hybridisation. Moreover, engorged ticks collected from the dogs were incubated at 28 °C to allow them to oviposit. Their subsequent larval progeny was also examined by PCR/RLB.

RESULTS

A total of 1085 ticks collected from 144 stray dogs at different residential areas consisted of 5 different species: H. hystricis (n = 435), R. sanguineus (n = 582), R. haemaphysaloides (n = 43), Amblyomma testudinarium (n = 14) and Ixodes ovatus (n = 11) were identified. Babesia gibsoni DNA was detected in H. hystricis females (10.3%), males (7.0%) and in 2.6% of the nymphs. One R. sanguineus female and one A. testudinarium female tick also carried B. gibsoni DNA. DNA of B. gibsoni was demonstrated in 11 out of 68 (16.2%) batches of larval ticks derived from engorged H. hystricus ticks only. Babesia vogeli DNA was detected only in R. sanguineus females (2.6%) and males (2.4%). DNA of B. vogeli was detected in 13 out of 95 (13.7%) batches of larval ticks derived from engorged R.sanguineus females.

CONCLUSIONS

Babesia gibsoni DNA was detected in the larval progeny of H. hystricis ticks only, whereas B. vogeli was restricted to the larvae of R. sanguineus. This provides evidence for transovarial passage of B. gibsoni in H. hystricis and evidence that this tick does act as the local vector for this parasite on dogs in northern Taiwan where most cases of babesiosis are reported. The vectorial capacity of R. sanguineus for babesiosis is probably restricted to the transmission of B. vogeli only.

摘要

背景

巴贝斯虫属(Babesia)是一种主要的蜱传原生动物血液寄生虫,影响整个东方地区的犬只。巴贝斯虫属由长角血蜱(Haemaphysalis longicornis)传播,而类似的角色也被认为是血红扇头蜱(Rhipicephalus sanguineus)。长角血蜱在台湾不存在,但血红扇头蜱广泛分布于犬只身上。然而,巴贝斯虫病的临床病例主要局限于该岛的北部。蜱的分布与临床病例之间的差异促使我们调查台湾北部犬只上的蜱种分布,目的是确定犬巴贝斯虫病的当地传播媒介。

方法

2015 年至 2017 年间,我们从台湾北部的流浪犬或自由放养的宠物犬身上采集蜱,并在鉴定后,使用 PCR 和反向线杂交(RLB)杂交检测蜱传巴贝斯虫寄生虫的存在。此外,从犬身上采集的饱血蜱在 28°C 下孵育,以使其产卵。随后还通过 PCR/RLB 检查其幼虫后代。

结果

从不同住宅区的 144 只流浪犬身上共采集了 1085 只蜱,包括 5 个不同的物种:硬蜱(H. hystricis)(n=435)、血红扇头蜱(R. sanguineus)(n=582)、血红扇头蜱(R. haemaphysaloides)(n=43)、赤鹿革蜱(A. testudinarium)(n=14)和扇头蜱(I. ovatus)(n=11)。在硬蜱的雌性(10.3%)、雄性(7.0%)和若虫(2.6%)中检测到巴贝斯虫属 DNA。一只血红扇头蜱雌性和一只赤鹿革蜱雌性蜱也携带巴贝斯虫属 DNA。仅从饱血硬蜱中分离出的 68 批幼虫(11 批,占 16.2%)中证实了巴贝斯虫属 DNA 的存在。巴贝斯虫属 vogeli DNA 仅在血红扇头蜱的雌性(2.6%)和雄性(2.4%)中检测到。从饱血血红扇头蜱雌性中分离出的 95 批幼虫(13 批,占 13.7%)中检测到巴贝斯虫属 vogeli DNA。

结论

仅在硬蜱的幼虫中检测到巴贝斯虫属 DNA,而巴贝斯虫属 vogeli 则局限于血红扇头蜱的幼虫。这为巴贝斯虫属在硬蜱中的经卵传递提供了证据,也证明了这种蜱在台湾北部是犬巴贝斯虫病的当地传播媒介,在那里报告了大多数巴贝斯虫病病例。血红扇头蜱的巴贝斯虫属传播能力可能仅限于巴贝斯虫属 vogeli 的传播。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cc98/5859485/ac0e629e10cc/13071_2018_2722_Fig1_HTML.jpg

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