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引用次数: 6
摘要
海龟第一次获得肠道菌群的方式和时间很大程度上是推测性的。本研究对红耳滑龟(Trachemys scripta elegans)的蛋壳和孵化过程在沙门氏菌初始感染中的作用进行了评价。首先,我们检查了蛋壳是否是细菌在孵化期间持续存在的可行底物,以及鸡蛋内部成分(即蛋白、蛋黄和胚胎)是否具有可检测的细菌负荷。其次,我们通过实验,用沙门氏菌和庆大霉素(一种有效的革兰氏阴性抗生素)联合处理鸡蛋来控制沙门氏菌。我们发现蛋壳是维持细菌的可行底物,也是沙门氏菌传播的有效屏障,因为鸡蛋内部成分基本上是无细菌的。在孵卵后18天收集的水样中,实验接种沙门氏菌的个体的鸡蛋比接种沙门氏菌但在孵卵前局部使用庆大霉素的鸡蛋、对照鸡蛋和仅使用庆大霉素的鸡蛋的沙门氏菌患病率更高,但在孵卵后35天,处理组之间没有明显差异。虽然蛋壳也可以作为屏障,防止细菌在孵化前感染胚胎,但这些发现表明,蛋壳可能是海龟孵化中沙门氏菌感染的一个来源。
How important is the eggshell as a source for initial acquisition of Salmonella in hatchling turtles?
How and when turtles first acquire gut microflora is largely speculative. In this study, the eggshell and hatching process were evaluated for their role in the initial acquisition of Salmonella, by red-eared slider turtles (Trachemys scripta elegans). First, we examined whether the eggshell is a viable substrate for bacterial persistence during incubation, and if internal egg components (i.e., albumen, yolk, and embryo) have detectable bacterial loads. Second, we experimentally manipulated Salmonella by treating eggs with combinations of Salmonella and gentamicin, an effective Gram-negative antibiotic. We found that the eggshell is a viable substrate for maintaining bacteria, as well as an effective barrier to Salmonella transmission as internal egg components were largely bacteria-free. Water samples collected 18 days post-hatch from individuals that were experimentally inoculated with a topical application of Salmonella as eggs had a higher prevalence of Salmonella than those from eggs inoculated with Salmonella but topically treated with gentamicin prior to hatching, control eggs, and eggs only treated with gentamicin, but by day 35 post-hatch there were no detectable differences among the treatment groups. Though it can also act as a barrier that prevents the bacteria from infecting the embryo prior to hatching these findings suggest that the eggshell is a likely source of Salmonella infection in turtle hatchlings.
期刊介绍:
The Journal Journal of Experimental Zoology Part A: Ecological Genetics and Physiology publishes articles at the three-way interface between Physiology, Ecology and Evolutionary Genetics. Contributions that help to elucidate how molecular, functional and ecological variation relate to one another are particularly welcome. The Journal publishes original research in the form of rapid communications or regular research articles, as well as perspectives and reviews on topics pertaining to the scope of the Journal. Acceptable articles are not limited to studies on animals, but also include research on plants and microbes.