硬蜱盾窝与盾窝腺的细微结构

用扫描及透射电镜研究硬蜱盾窝与盾窝腺的结构.幼蜱只有横缝状盾窝原基,盾窝腺尚未发育;若蜱盾窝增大,其孔数相应增加;到成蜱阶段,不仅盾窝增大,而且盾窝腺完成发育.对9种雌蜱盾窝进行比较,在其大小和孔数方面有一定差别.亚洲璃眼蜱雄蜱盾窝腺不发达,几个叶瓣贴在一起,组成1—2个腺体组.雌蜱吸血前,叶瓣相互贴在一起.吸血后,球状叶瓣散开,连接叶瓣的导管清楚可见,分泌细胞中颗粒增多,这与其分泌性信息素有关.     

孤雌生殖长角血蜱的哈氏器超微结构与发育

为阐明长角血蜱Haemaphysalis longicornis孤雌生殖种群的哈氏器结构及发育特征, 用扫描电镜对其各虫期哈氏器进行了观察, 分析了血餐对哈氏器发育的影响。结果表明： 该种群幼蜱、 若蜱和成蜱哈氏器形态结构基本相同, 均由前窝和后囊构成。幼蜱前窝感毛6根, 位于同一基盘; 若蜱和成蜱哈氏器相似, 前窝感毛7根, 其中1根孔毛位于外侧基盘, 另6根感毛位于内侧基盘。各虫期饱血后哈氏器大小均比饥饿状态下显著增大（P<0.05）。幼蜱前窝与后囊面积比值与若蜱相比无显著差异（P>0.05）, 若蜱前窝与后囊面积比值与成蜱相比差异显著（P<0.05）。各虫期哈氏器均在发育, 且血餐对哈氏器发育有重要影响。幼蜱至若蜱期哈氏器前窝与后囊的发育速度相似, 若蜱至成蜱期哈氏器前窝发育快于后囊。本研究结果在一定程度上揭示了孤雌生殖长角血蜱的哈氏器发育规律。     

硬蜱盾窝腺释放性信息素

用生物测定和对盾窝进行x-射线微区分析相结合的方法,研究了亚洲璃眼蜱雌蜱性信息素的释放与吸血和交配的关系.生物测定结果表明:雌蜱通过盾窝释放性信息素,有性活力动能的雄蜱有所反应,爬向雌蜱进行交配.雌蜱吸血后第1天,有反应的雄蜱数目显著增加;吸血后的第3—5天,有反应的雄蜱数目达到最高峰,交配后有反应雄蜱的数目明显下降.如果用指甲油封闭雌蜱盾窝,有反应的雄蜱数目显著减少.由于性信息素的有效成分为2,6-二氯酚,故用x-射线微区分析方法测定盾窝氯含量的变化,可以表明雌蜱性信息素的释放量,其结果与生物测定结果一致:未吸血的雌蜱台氯水平为0.62,吸血后第1—2天均增到5.87,有非常显著的差异(P<0.001).吸血后第3—5天含氯水平为10.23,达到最高峰,与吸血后第1—2天的相比,差异也很显著(p<0.001).与雄蜱交配后含氯不平又降至0.89,性信息素含量明显降低,与来吸血的雌蜱含量接近.     

伊维菌素对长角血蜱生长发育及生殖的影响

【目的】通过分析宿主皮下注射伊维菌素对长角血蜱生长发育及生殖的影响,进而评价伊维菌素对长角血蜱的防治效果。【方法】以新西兰白兔为宿主,皮下注射不同剂量伊维菌素,观察幼蜱、若蜱及雌蜱的叮咬率、死亡率、吸血期、饱血体重、产卵量和孵化率等生物学参数,分析伊维菌素对长角血蜱生殖和生长发育的影响。【结果】伊维菌素对长角血蜱各期蜱虫的叮咬率均无显著影响。与对照组相比,伊维菌素可显著增加幼蜱和若蜱死亡率,延长若蜱和雌蜱的吸血期并降低其饱血体重,降低雌蜱产卵量及卵孵化率,抑制卵巢及卵的发育。【结论】宿主皮下注射伊维菌素能够显著抑制长角血蜱的发育及生殖,可作为防治长角血蜱的候选杀虫剂。     

中华硬蜱、越原血蜱和青海血蜱经期传播莱姆病螺旋体的实验研究

以实验室培育的非感染中华硬蜱、越原血蜱和青海血蜱刺叮人工感染21天的阳性KM鼠,利用分离培养和PCR方法检测蜱对莱姆病螺旋体Borrelia garinii的保持能力以及体内螺旋体对敏感动物的感染能力。中华硬蜱、越原血蜱和青海血蜱非感染幼蜱均可以通过吸血获得莱姆病螺旋体, 然而,它们在饱血、消化、蜕皮和再次吸血过程中对莱姆病螺旋体的保持能力差异很大。只有中华硬蜱可以保持活的莱姆病螺旋体直至蜕化为下一发育阶段,蜕化后仍携带莱姆病螺旋体并对敏感KM鼠有感染能力。而越原血蜱和青海血蜱对莱姆病螺旋体的保持能力不能跨越消化、蜕皮阶段,蜕化后这两种血蜱不再携带莱姆病螺旋体,因此,这两种血蜱不具备经期传播能力,作为莱姆病媒介的可能性不大。中华硬蜱于幼蜱到若蜱以及若蜱到成蜱两个阶段均具备经期传播莱姆病螺旋体的能力,提示了中华硬蜱作为南方莱姆病的潜在媒介是可能的。     

森林革蜱、草原革蜱感染和经期传播莱姆病螺旋体的实验研究

以实验室培育的非感染森林革蜱Dermacentor silvarum、草原革蜱D. nuttalli刺叮人工感染21天后的阳性KM鼠,利用分离培养和PCR方法检测蜱对螺旋体的保持能力以及体内螺旋体对敏感动物的感染能力。结果如下：非感染幼蜱均可以通过吸血获得莱姆病螺旋体,饱血森林革蜱和草原革蜱幼蜱PCR阳性率均为50.0%而分离阳性率都为20.0%。饱血脱落后,这些幼蜱只能在饱血后2天内分离到莱姆病螺旋体。PCR检测阳性也只能持续到4天,均不能跨越蜕皮阶段。蜕化为若蜱后,若蜱以及分别受到这些若蜱刺叮的KM鼠均未发现阳性感染。非感染若蜱吸食感染的KM鼠后,饱血森林革蜱和草原革蜱获得了莱姆病螺旋体,PCR检测阳性率分别为50.0%和20.0%。分离阳性率分别达到33.3%和60.0%。这些若蜱分别于饱血后2天和3天可以分离到莱姆病螺旋体,PCR扩增阳性也只能分别持续到饱血后4天和6天,均不能跨越蜕皮阶段;蜕化为成蜱后,成蜱以及受到它们攻击的KM鼠均未获阳性检测结果。同种蜱不同地理株在感染和保持莱姆病螺旋体的能力上也没有差异。森林革蜱、草原革蜱的幼蜱和若蜱虽可以吸血感染但均不具备经期传播莱姆病螺旋体Borrelia garinii CHNM4的能力,作为莱姆病媒介的可能性不大。     

昆虫病原线虫斯氏线虫和异小杆线虫对长角血蜱雌蜱的致病力

用昆虫病原线虫小卷蛾斯氏线虫（Sc BJ）、夜蛾斯氏线虫（Sf Otio）、拟双角斯氏线虫（Sc D43）、格氏斯氏线虫（Sg NC32）和嗜菌异小杆线虫（Hb E-6-7）对长角血蜱雌蜱进行感染试验,所用线虫剂量为4 000 Ijs/dish。结果表明,5种线虫均对长角血蜱雌蜱有致死效应。Hb E-6-7和Sc BJ两种线虫对雌蜱各发育期致病力最强,导致雌蜱的累积死亡率和半致死时间分别为饥饿雌蜱82.5%,9.0天和75.0%,8.8天;吸血雌蜱90.0%,8.0天和82.5%,8.0天;饱血雌蜱93.3%,7.3天和86.7%,7.3天。Sc D43对饱血雌蜱有较高的致死效应,为80.0%,但半致死时间较长,为11.7天。Sf Otio和Sg NC32对长角血蜱雌蜱的致死效应较低。饱血雌蜱较饥饿雌蜱和吸血雌蜱更易被线虫感染。     

蜱类血淋巴的收集方法

建立一种收集蜱类血淋巴的有效方法。饥饿雌蜱切割边缘体壁收集,每只雌蜱可收集血淋巴0.4μL;吸血、饱血雌蜱切割附肢收集,每只饱血雌蜱可收集8.0μL血淋巴。该方法操作简单、快速、收集量较大。     

长角血蜱幼虫中的蜕皮甾类(英文)

本文用放射免疫分析和高效液相色谱法对长角血蜱幼虫中的蜕皮甾类进行了测定。　蜕皮甾类存在于吸血和饱血幼虫,并且随生理时期而变化。吸血期和饱血后前３天,激素含量低（小于 １４． ３５ｐｇ ＥＥ／只）;饱血后５天迅速上升（２９．８７ｐｇ ＥＥ／只）;饱血后７天达到高峰（５６． ０４ｐｇ ＥＥ／只）;高峰后又下降到低水平（１９．３８ ｐｇＥＥ／只）。高峰期的蜕皮甾类主要为两种成分,２０Ｅ和Ｅ（２０Ｅ∶Ｅ＝３．０７∶１）。２０Ｅ可能是幼虫发育中起主要作用的激素。     

实验室条件下长角血蜱的生物学特性研究

实验室条件[(27±1)℃;75%RH;6L：18D]下,长角血蜱完成其生活史需135.8d：卵的孵化期为38.5d：幼虫吸血前期、吸血期和蜕皮前期分别为5.3d,3.8d和13.9d;若虫吸血前期、吸血期和蜕皮前期分别为7.2d,5.4d和16.9d;成虫吸血前期、吸血期、产卵前期和产卵期分别为7.6d,9.4d,7.8d和20.0d。雌虫饱食体重与产卵量之间存在非常显著的正相关(r＝0.9496,P<0.001)。雌虫的生殖效率指数REI＝11.06,生殖适合度指 数RFI＝7.19。生活周期在不同季节无明显变化。雄虫吸血期受雌虫吸引而成功地交配,这一过程是在吸引性信息素的作用下完成的。     

Morphology of the foveal glands and foveae dorsales in male Hyalomma truncatum and Rhipicephalus evertsi mimeticus ticks (Acari; Ixodidae) before and during feeding

The ultrastructure of the foveae dorsales and foveal glands in unfed and attached male Hyalomma truncatum and Rhipicephalus evertsi mimeticus ticks was studied. Both species are provided with a paired foveal gland system, which is similar in unfed as well as in attached ticks. This gland system consists of the fovea dorsalis with pores and pore tubes as the external part, the foveal neck zone as a link between the fovea dorsalis and the lobes of the gland and the bulbous lobes as the innermost part. The fovea dorsalis is located on either side of the dorsal midline in the midsection of the body and appears as a roundish plate containing 15±6.5 and 21±7 slit-like pores in R. evertsi mimeticus (n=210) and H. truncatum (n=210), respectively. Each pore leads into a cuticular lined channel containing a pore tube. Below each fovea, the foveal neck zone is located within a groove of the cuticle and consists of the termini of the pore tubes which enlarge basally to form a cup-shaped ampulla each. Furthermore, secretory lobes are located below the foveal neck zone. Each lobe consists of secretory cells and a central excretory duct which leads into the ampulla. The ducts are lined with microvilli. The secretory cells contain numerous vesicles of varying size with one or more granules. In male ticks of both species the secretory lobe cells remained unchanged in size, structure and granule content irrespective of whether they were unfed or attached for up to 30 days. Axons occur in the fascicles between the secretory lobe cells containing numerous neurosecretory vesicles. A possible role of the foveal glands in the production of pheromones is hypothesized.     

Transstadial transmission of Theileria annulata through common ixodid ticks infesting Indian cattle.

Transstadial transmission of Theileria annulata with Hyalomma anatolicum anatolicum, H. dromedarii and H. marginatum isaaci, and Haemaphysalis bispinosa, Rhipicephalus haemaphysaloides haemaphysaloides and Boophilus microplus was determined. It was found that the infection was successfully transmitted by H. a. anatolicum from larva to nymph and nymph to adult in all attempts. When larvae were fed on an infected calf the succeeding adults transmitted the infection when the intervening nymphs fed on a rabbit (non-susceptible host) but not when fed on a calf (susceptible host). Infective adult ticks transmitted the parasite during the first 24 h of feeding on a calf. When the feeding was interrupted after 24 h, and the tick transferred to another calf, the infection was transmitted to the latter as well. H. dromedarii successfully transmitted the infection from larva to nymph and from nymph to adult. Larvae of H. marginatum isaaci did not feed on calves but the infection was successfully transmitted from nymph to adult. Haemaphysalis bispinosa, Rhipicephalus h. haemaphysaloides and Boophilus microplus did not transmit Th. annulata from larva to nymph to adult.     

Description of a new argasid tick (Acari: Ixodida) from bat caves in Brazilian Amazon

Nothoaspis amazoniensis n. sp. (Acari: Ixodida: Argasidae) is described from adult and immature ticks (nymph II, nymph I, larva) collected from bat caves in the Brazilian Amazon. Also, 16S rDNA sequences are provided. The diagnostic characters for adults are the presence of false shield or nothoaspis, an anteriorly projecting hood covering the capitulum, a medial extension of palpal article I (flaps), genital plate extending from coxa I to IV, absence of 2 setae on the internal margin of the flaps, a minute hypostome without denticles, presence of a central pore in the base of hypostome, and a reticulate surface pattern on the posterior half of the nothoaspis in males. The nymph II stage is characterized by a hood that is small in relation to the capitulum, short coxal setae, palpal flaps lacking setae on the internal margin, long hypostome, pointed with dentition 4/4 apically, and the anterior half of the body is covered by a cell-like configuration. Nymph I stage is characterized by a hood, small in relation to the capitulum, dorsum of the body covered by a cell-like configuration, venter integument covered by a cell-like configuration, and hypostome dentition 4/4 with apices that are "V"-shaped. Diagnostic characters of the larvae are the number and size of dorsal setae, and the shape of scutum and hypostome. The new species appears to have a life cycle with a larva that feeds on bats, a non-feeding nymphal stage (nymph I), a feeding nymphal stage (nymph II), and adults that probably represent non-feeding stages.     

The life cycle of Hyalomma rufipes (Acari: Ixodidae) under laboratory conditions

Biological characteristics of Hyalomma rufipes parasitising on rabbits and sheep were compared under laboratory conditions in Gansu, China. Mature ticks could parasitize both rabbits and sheep, while immature ticks only fed on rabbits successfully. Adults sucked blood on sheep significantly longer than on rabbits (16 and 13 days, respectively). Other adult parasite characteristics fed on the two hosts were similar, including the weight of engorged adult, female daily oviposition, and the weight and amount of the egg mass laid. Those indicated that this tick species showed little host specificity between sheep and rabbits during its adult stage. In total, the life cycle of H. rufipes was completed in an average period of 179 days. The average developmental periods were 59 days for egg incubation, 3 and 21 days for immature tick prefeeding and feeding, 2, 12 and 40 days for adult prefeeding, female preoviposition and oviposition. The longer female fed for engorgement, the shorter preoviposition period of engorged female needed, although when the feeding period was less than 15 days, this relationship was not obvious. The results confirmed the correlation between the weight of the engorged female and the number of eggs laid (r = 0.909). The reproductive efficiency index (REI) and reproductive fitness index (RFI) in females was 10.63 and 7.22, respectively. Engorged nymphs moulting to females were significantly heavier (27.6 ± 0.89 mg) than those moulting to males (22.3 ± 0.52 mg). Males outnumbered females by 1.4:1.     

Reason for fluctuation in the demographic structure of the taiga tick population (Ixodidae) in dark conifer-leaf forests of Kemchug Upland

It was found out, that mean ratio of unfed taiga ticks Ixodes persulcatus having a life cycle of 3-5 and 6 years counts respectively (N = 6) 33.6, 52.8, 13.2 and 0.4%. Data on absolute number of I. persulcatus individuals in the process of onthogenesis is given. It is shown, that mortality of different unfed stages increases from larva to imago. In the autumn-winter period, the mean ratio of eliminated individuals counted 16% of larvae, 20% of nymphs, and 38 of imago. The mortality in the spring-summer period caused mainly by the deficit of hosts and counted for these stages 3, 82 and 98% respectively. Engorged ticks successfully undertake unfavorable conditions both in the spring-summer and autumn-winter periods. Their mean mortality in the period from feeding to moulting does not exceed 12%.     

Aspects of the life history of Cercopithifilaria johnstoni (Nematoda:Filarioidea)

and 1988. Aspects of the life history of Cercopithifilaria johnstoni (Nematoda:Filarioidea). International Journal for Parasitology 18: 1087–1092. Cercopithifilaria johnstoni (Nematoda:Filarioidea) occurs in the subcutaneous connective tissues of a spectrum of native murid and marsupial hosts in Eastern Australia. Life cycle studies revealed that: (i) microfilaria occur in lymphatic capillaries and extravascular connective tissue of the dermis (= ‘skin-inhabiting’), (ii) ixodid ticks, particularly Ixodes trichosuri, are intermediate hosts in nature, (iii) development from microfilariae to infective third-stage larva occurs only while the tick is off the host, that is, during ecdysis from larva to nymph or from nymph to adult. Transmission of C. johnstoni in a wild population of bush rats (Rattus fuscipes) occurred in summer and winter, and was associated with peaks in the number of larval and/or nymphal stages of ticks on rats. C. johnstoni was transmitted experimentally to bandicoots (Isoodon macrourus, Perameles nasuta), bush rats and laboratory rats (R. norvegicus), indirectly by subcutaneous inoculation of third-stage larvae and directly by tick feeding. The prepatent period was approximately 3 months and the longest duration of microfilariae in the ‘ skin’ was more than 25 months. Dermal and ocular lesions were observed in R. fuscipes. The host-parasite relationship has the potential for development as an inexpensive and practical model for human onchocerciasis.     

Ticks feeding on northern pocket gophers (Thomomys talpoides) in central Saskatchewan and the unexpected detection of Ixodes scapularis larvae

Morphological examination of ticks feeding on northern pocket gophers, Thomomys talpoides, near Clavet (Saskatchewan, Canada) revealed the presence of two genera, Ixodes and Dermacentor. All adult ticks collected were identified as I. kingi. Single strand conformation polymorphism (SSCP) analyses and DNA sequencing of the mitochondrial 16S rRNA gene confirmed the species identity of most Ixodes immatures as I. kingi (two nymphs and 82 larvae), and the Dermacentor immatures as D. variabilis (one nymph and one larva) and D. andersoni (three larvae). Six Ixodes larvae feeding on three T. talpoides individuals were identified as four different 16S haplotypes of I. scapularis, which was unexpected because there are no known established populations of this species in Saskatchewan. However, flagging for questing ticks and further examination of the ticks feeding on T. talpoides in two subsequent years failed to detect the presence of I. scapularis near Clavet, suggesting that there is no established population of I. scapularis in this area. Nonetheless, since I. scapularis is a vector of pathogenic agents, passive and active surveillance needs to be conducted in Saskatchewan on an ongoing basis to determine if this tick species and its associated pathogens become established within the province.