首页 | 本学科首页   官方微博 | 高级检索  
相似文献
 共查询到16条相似文献,搜索用时 198 毫秒
1.
从70年代以来,应用气相色谱法分析医学昆虫表皮烃类碳的波形,能有效地鉴别复组的亲缘种类(sibling species),包括蚊、蚋、釆釆蝇等重要传病媒介,已成为昆虫的化学分类法(Carlson, 1984; Phillips & Milligan, 1986)。本文试用气相色谱法鉴别尖音库蚊(Culex pipiens Complex)的淡色库蚊(Culex pipiens pallens)北京株、致倦库蚊(Culex quinquefasciatus)的武汉株和广州株。  相似文献   

2.
中国尖音库蚊复合组杂交的研究   总被引:8,自引:1,他引:7  
本文对分布在我国的尖音库蚊复合组的尖音库蚊,致倦库蚊和淡色库蚊进行杂交研究,结果表明致倦库蚊与尖音库蚊及淡色库蚊以及两者尖交可以产生能育的F1代,它们之间没有传统意义上的生殖隔离,致倦库蚊应为尖音库蚊是的一个亚种,而不是如国外有些学者认为的独立种,另外,杂种F2代成活率很低,这有可能是尖音库蚊(广义)种下分化在遗传学上的反映。  相似文献   

3.
我国尖音库蚊复合组蚊虫的杂交及其与Wolbachia感染的关系   总被引:1,自引:1,他引:0  
为了了解我国尖音库蚊复合组蚊虫间杂交卵的不孵化现象和明确该现象与共生微生物Wolbachia感染的关系,对该复合组实验室种群4个亚种进行了笼内杂交和抗生素处理后的杂交。试验表明: 在复合组蚊虫中骚扰库蚊Culex pipiens molestus与淡色库蚊Cx. Pipiens pallens、致倦库蚊Cx. Ipiens quinquefasciatus与尖音库蚊Cx. Pipiens pipiens之间存在有单向胞质不融合现象,骚扰库蚊的雄虫与尖音库蚊、致倦库蚊和淡色库蚊的雌虫杂交卵的孵化率分别为0.06%、0.46%和0.19%;该胞质不融合现象可以通过抗生素处理而消除,处理后骚扰库蚊雄虫与其余3个亚种雌虫F3杂交卵的孵化率均有提高,分别为89.49%(t=3.90×10-28t0.01=2.704)、23.39%(t=9.15×10-7t0.01=2.660和22.27%(t=5.08×10-4t0.01=2.750),并可因抗生素处理而产生新的不融合类型。  相似文献   

4.
赵彤言  陆宝麟 《昆虫学报》1994,37(4):446-449
本文报道了我国23个不同地区的尖音库蚊复合组(Culex pipiens complex)雄蚊阳茎DV/D的数值分析结果。经过多元相关与回归分析发现,雄蚊阳茎DV/D的比值与纬度、经度之间存在着负相关的关系,并建立了DV/D与纬度的单元回归方程,以及DV/D与纬度、经度之间的多元回归方程。根据DV/D=0.5为区分淡色库蚊和致倦库蚊的一般标准,从回归方程中求得北纬30°左右为我国淡色库蚊和致倦库蚊地理分布的理论分界线。  相似文献   

5.
中国尖音库蚊复合组支序系统学的研究   总被引:3,自引:1,他引:2  
本文应用支序系统学原理和方法,采用形态和生态性状,对尖音库蚊复合组的4个成员进行了支序系统学研究,提出在尖音库蚊复合组中,尖音库蚊是原始的类群,骚扰库蚊为较进化的类群,而致倦库蚊和淡色库蚊是最为进化的类群。  相似文献   

6.
<正> 我们对我国较重要的3属8种蚊虫的声频进行了测定(其中3种在文献中有记载),结果如下。 材料和方法 蚊虫 淡色库蚊Culex pipiens pallens、致倦  相似文献   

7.
几种蚊虫线粒体DNA-16SrRNA序列及其相互关系的研究   总被引:10,自引:1,他引:9  
测定我国尖音库蚊复合组4亚种(尖音库蚊、淡色库蚊、致倦库蚊和骚扰库蚊)、三带喙库蚊、白纹伊蚊和中华按蚊的线粒体DNA 16S rRNA基因(mtDNA-16S rRNA)序列,发现我国尖音库蚊复合组4亚种mtDNA-16S rRNA序列基本一致,长度为555bp(554bp),GC含量为25.41%。该序列与其他3种蚊虫在种间存在差异,与三带喙库蚊的种间差异为0.54%;与白纹伊蚊的种间差异为5.77%;与中华按蚊的种间差异为9.62%。分子系统关系分析表明该序列与传统分类系统的同属或同亚科种类近似性相一致。  相似文献   

8.
WS-I型灭蚊涂料对防制淡色库蚊、家蝇等的敏感性已有报道。但对南方夜间常见侵入室内的中华按蚊(Anopheles sinensis)、致倦库蚊(Culex pipiens fatigans)和三带喙库蚊(Culex tritaeniorhychus)的敏感性及对不同状态致倦库蚊的敏感性如何尚未见报道,为此于1987年6月作了实验,现将结果报道于后:WS-I型灭蚊涂料(主含杀灭菊酯),由本地黄沙河灭蚊涂料厂提供;吸血成蚊均捕自牛房,未吸血致倦库蚊为实验室羽化;用“WHO”接触筒,将涂料按每平方0.33公斤用量涂于新华Ⅰ号滤纸上待干后进行测定,吸血蚊以胃血谢拉氏Ⅲ—Ⅳ期、未吸血蚊以5%葡萄糖水…  相似文献   

9.
蚊的吸血量是蚊生态习性的一个重要方面。致倦库蚊(Culex pipiens quinquefasciatus)分布于全世界热带及亚热带,在我国则分布北纬33°以南广大地区,是我国班氏丝虫病的主要传播媒介之一,且与乙型脑炎的传播有关。为此对其吸血量进行了初步实验观察。1 材料和方法试验所用的致倦库蚊蚊株采自武汉市区,经实验室驯化饲养近2年。饲养条件为温度22  相似文献   

10.
在饲养致倦库蚊(Culex pipiens quinquefasciatus)和中华按蚊(Anopheles sinensis)的过程中,发现雌蚊吸一次血后致倦库蚊产卵时间很长,中华按蚊产卵时间较短,为了搞清楚这两种不同属的蚊虫产卵习性的差异,我们于1992年进行了这两种蚊的产卵习性实验观察。1 材料与方法  相似文献   

11.
Abstract The present paper is the results of the biosystematic studies of Culex pipiens complex in China, including hybridization, mathematical analyses of morphological characters and GC analyses of culticular hydrocarbons. On the bases of the results of these studies, in addition to their allopatric distribution, it can be concluded that Cx. pipiens complex in China consists of four subspecies, including Cx. p ipiens molestus recently discovered in Beijing. Cx. pipiens quinquefasciatus can not be considered as a spearate species and Cx. pipiens pallens is not an intermediate form as claimed by some western workers.  相似文献   

12.
Culex pipiens complex mosquitoes are widely distributed throughout China and are known to be important disease vectors. Two pyrethroid resistance associated mutations have been identified in Cx. pipiens complex (Diptera: Culicidae), but there is little information on the diversity and distribution of kdr alleles in pyrethroid resistance in Cx. pipiens complex mosquitoes in China. In the present study, we report on a modified three tube allele-specific (AS)-PCR method for detecting the 1014F and 1014S alleles. The new technique was applied to identify the distribution of the two alleles in natural Cx. pipiens complex populations in China. The results confirmed that the new method is both sensitive and specific. The 1014F allele was found in all 14 of the field populations tested (frequency ranged from 6.8 to 76.2%) and the 1014S allele was found in almost two-thirds (frequency from 2.4 to 28.6%), indicating that the genotypes known to be associated with pyrethroid resistance are widespread in China. The resistance-associated alleles were more common in southern Chinese sampling sites than in northern sites. The coexistence of the two resistant mutations in individual mosquitoes was also observed in five of the field populations. Two alternative mutations within the L1014 codon were identified in Culex pipiens molestus Forskal, 1775, including a non-synonymous mutation resulting in a 1014C substitution.  相似文献   

13.
我国蚊虫体内感染的Wolbachia的wsp基因序列测定与分析   总被引:3,自引:2,他引:1  
测定了我国尖音库蚊复合组和白纹伊蚊蚊虫体内感染的Wolbachia株的wsp基因序列。核苷酸和氨基酸的同源性及系统关系分析表明,我国尖音库蚊复合组和白纹伊蚊中Wolbachia株的wsp基因序列与Pip组其它株的核苷酸及氨基酸同源性分别为98%~100%和97%~100%, 属B大组Wolbachia中的Pip组。  相似文献   

14.
Mosquitoes in the Culex pipiens complex thrive in temperate and tropical regions worldwide, and serve as efficient vectors of Bancroftian lymphatic filariasis (LF) caused by Wuchereria bancrofti in Asia, Africa, the West Indies, South America, and Micronesia. However, members of this mosquito complex do not act as natural vectors for Brugian LF caused by Brugia malayi, or for the cat parasite B. pahangi, despite their presence in South Asia where these parasites are endemic. Previous work with the Iowa strain of Culex pipiens pipiens demonstrates that it is equally susceptible to W. bancrofti as is the natural Cx. p. pipiens vector in the Nile Delta, however it is refractory to infection with Brugia spp. Here we report that the infectivity barrier for Brugia spp. in Cx. p. pipiens is the mosquito midgut, which inflicts internal and lethal damage to ingested microfilariae. Following per os Brugia exposures, the prevalence of infection is significantly lower in Cx. p. pipiens compared to susceptible mosquito controls, and differs between parasite species with <50% and <5% of Cx. p. pipiens becoming infected with B. pahangi and B. malayi, respectively. When Brugia spp. mf were inoculated intrathoracically to bypass the midgut, larvae developed equally well as in controls, indicating that, beyond the midgut, Cx. p. pipiens is physiologically compatible with Brugia spp. Mf isolated from Cx. p. pipiens midguts exhibited compromised motility, and unlike mf derived from blood or isolated from the midguts of Ae. aegypti, failed to develop when inoculated intrathoracically into susceptible mosquitoes. Together these data strongly support the role of the midgut as the primary infection barrier for Brugia spp. in Cx. p. pipiens. Examination of parasites recovered from the Cx. p. pipiens midgut by vital staining, and those exsheathed with papain, suggest that the damage inflicted by the midgut is subcuticular and disrupts internal tissues. Microscopic studies of these worms reveal compromised motility and sharp bends in the body; and ultrastructurally the presence of many fluid or carbohydrate-filled vacuoles in the hypodermis, body wall, and nuclear column. Incubation of Brugia mf with Cx. p. pipiens midgut extracts produces similar internal damage phenotypes; indicating that the Cx. p. pipiens midgut factor(s) that damage mf in vivo are soluble and stable in physiological buffer, and inflict damage on mf in vitro.  相似文献   

15.
Due to cytoplasmic inheritance, spread of maternally inherited Wolbachia symbionts can result in reduction of mitochondrial variation in populations. We examined sequence diversity of the mitochondrial NADH dehydrogenase subunit 4 (ND4) gene in Wolbachia-infected (South Africa (SA), California and Thailand) and uninfected (SA) Culex pipiens complex populations. In total, we identified 12 haplotypes (A-L). In infected populations, 99% of individuals had haplotype K. In the uninfected SA population, 11 haplotypes were present, including K. Nuclear allozyme diversity was similar between infected and uninfected SA populations. Analysis of nuclear DNA sequences suggested that haplotype K presence in uninfected SA Cx. pipiens was probably due to a shared ancestral polymorphism rather than hybrid introgression. These data indicate that Wolbachia spread has resulted in drastic reduction of mitochondrial variability in widely separated Cx. pipiens complex populations. In contrast, the uninfected SA population is probably a cryptic species where Wolbachia introgression has been prevented by reproductive isolation, maintaining ancestral levels of mitochondrial diversity. Molecular clock analyses suggest that the Wolbachia sweep occurred within the last 47000 years. The effect of Wolbachia on mitochondrial dynamics can provide insight on the potential for Wolbachia to spread transgenes into mosquito populations to control vector-borne diseases.  相似文献   

16.
Seasonal epizootics of vector-borne pathogens infecting multiple species are ecologically complex and difficult to forecast. Pathogen transmission potential within the host community is determined by the relative abilities of host species to maintain and transmit the pathogen and by ecological factors influencing contact rates between hosts and vectors. Increasing evidence of strong feeding preferences by a number of vectors suggests that the host community experienced by the pathogen may be very different from the local host community. We developed an empirically informed transmission model for West Nile virus (WNV) in four sites using one vector species (Culex pipiens) and preferred and non-preferred avian hosts. We measured strong feeding preferences for American robins (Turdus migratorius) by Cx. pipiens, quantified as the proportion of Cx. pipiens blood meals from robins in relation to their abundance (feeding index). The model accurately predicted WNV prevalence in Cx. pipiens at three of four sites. Sensitivity analysis revealed feeding preference was the most influential parameter on intensity and timing of peak WNV infection in Cx. pipiens and a threshold feeding index for transmission was identified. Our findings indicate host preference-induced contact heterogeneity is a key mediator of vector-borne pathogen epizootics in multi-species host communities, and should be incorporated into multi-host transmission models.  相似文献   

设为首页 | 免责声明 | 关于勤云 | 加入收藏

Copyright©北京勤云科技发展有限公司  京ICP备09084417号