首页> 外文期刊>Folia microbiologica >Wolbachia and bacteriophage WO-B density of Wolbachia A-infected Aedes albopictus mosquito.
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Wolbachia and bacteriophage WO-B density of Wolbachia A-infected Aedes albopictus mosquito.

机译:Wolbachia A感染的 albopictus 蚊子的 Wolbachia 和噬菌体WO-B密度。

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Wolbachia are maternally inherited symbiotic bacteria capable of inducing an extensive range of reproductive abnormalities in their hosts, including cytoplasmic incompatibility (CI). Its density (concentration) is likely to influence the penetrance of CI in incompatible crosses. The variations of Wolbachia density could also be linked with phage WO density. We determined the relative density (relative concentration) of prophage WO orf7 and Wolbachia (phage-to-bacteria ratio) during early developmental and adult stages of singly infected Aedes albopictus mosquito (Wolbachia A-infected) by using real-time quantitative PCR. Phage WO and Wolbachia did not develop at the same rate. Relative Wolbachia density (bacteria-to-host ratio) was high later in development (adult stages) whilst relative prophage WO density (phage-to-bacteria ratio) was low in the adult stages. Furthermore, 12-d-old adults of singly infected female mosquito had the highest Wolbachia density. In contrast, the larval stage 4 (L4) contained the highest prophage WO-B orf7 density. The association of hosts-Wolbachia-phage among diverse species is different. Thus, if phage and Wolbachia are involved in Cl mechanism, the information of this association should be acquired for each specific type of organism for future use of population replacement or gene drive system.
机译:Wolbachia 是母体遗传的共生细菌,能够在其宿主中诱发广泛的生殖异常,包括细胞质不相容性(CI)。它的密度(浓度)可能会影响不相容杂交物中CI的渗透率。沃尔巴氏菌密度的变化也可能与噬菌体的WO密度有关。我们确定了在单独感染白纹伊蚊(ied albopictus )蚊子的早期发育和成年阶段,噬菌体WO orf7和 Wolbachia 的相对密度(相对浓度)(噬菌体与细菌的比率)(通过实时定量PCR感染 Wolbachia A)。噬菌体WO和 Wolbachia 的发育速度不同。相对的沃尔巴氏菌密度(细菌与宿主的比率)在发育后期(成年阶段)较高,而成年阶段的相对噬菌体WO密度(噬菌体与细菌比率)则较低。此外,单次感染的雌性蚊子的12 d成年成年人的 Wolbachia 密度最高。相反,幼虫阶段4(L4)包含最高的原噬菌体WO-B orf7密度。不同物种之间宿主-沃尔巴氏菌-噬菌体的关联是不同的。因此,如果噬菌体和 Wolbachia 参与Cl机制,则应获取每种特定类型生物的这种关联信息,以供将来使用种群替代或基因驱动系统。

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