夏威夷短尾鱿鱼(Euprymna scolopes)附属腺体及相关细菌群落的发育。

IF 2.1 4区 生物学 Q2 BIOLOGY
Biological Bulletin Pub Date : 2021-06-01 Epub Date: 2021-04-22 DOI:10.1086/713965
Allison H Kerwin, Sarah J McAnulty, Spencer V Nyholm
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引用次数: 5

摘要

摘要夏威夷短尾乌贼(Euprymna scolopes)有一个雌性生殖器官,称为附属腺,其中包含一个共生细菌联合体。这些细菌从附属腺体沉积到鱿鱼的卵壳中,在那里联合体防止微生物污染。共生体群落在宿主种群中是环境传播和保守的,但对器官如何发育和被细菌定植知之甚少。为了更好地了解镜下腺的发育过程,我们利用组织学、共聚焦显微镜和透射电镜对其成熟过程进行了表征。我们发现,在孵化后大约四周,首先形成了一个上皮场,随后是许多毛孔的增殖,我们假设这是细菌招募的开始(早期发育)。显微镜检查显示,这些毛孔与偶尔含有细菌的纤毛内陷相连。在发育中期,这些上皮场扩大,在上皮层下观察到独立的定植小管,其中包含孔和内陷。在发育后期,当动物接近性成熟时,表面上皮区出现退化,并且在完全成熟的成年动物(孵化后约2-3个月)中从未观察到,这表明它们有助于辅助网膜的细菌定植。通过对不同大小的雌性辅助网膜腺16S rRNA基因多样性的分析发现,随着寄主性成熟的临近,细菌群落发生了变化,群落均匀性增加,从verrucomicrobia为主转变为alphaproteobacteria为主。鉴于寄主与光器官共生体费氏弧菌(Vibrio fischeri)的关系,我们的研究表明,E. scolopes的附属网膜腺可能具有类似的从环境中招募细菌的机制。了解副基底腺的发育和定植过程将扩大E. scopes作为研究海洋共生细菌联合体的模式生物的应用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Development of the Accessory Nidamental Gland and Associated Bacterial Community in the Hawaiian Bobtail Squid, Euprymna scolopes.

AbstractThe Hawaiian bobtail squid, Euprymna scolopes, has a female reproductive organ called the accessory nidamental gland that contains a symbiotic bacterial consortium. These bacteria are deposited from the accessory nidamental gland into the squid's egg cases, where the consortium prevents microbial fouling. The symbiont community is environmentally transmitted and conserved across host populations, yet little is known about how the organ develops and is colonized by bacteria. In order to understand accessory nidamental gland development in E. scolopes, we characterized the gland during maturation by using histology and confocal and transmission electron microscopy. We found that an epithelial field formed first about four weeks after hatching, followed by the proliferation of numerous pores during what we hypothesize to be the initiation of bacterial recruitment (early development). Microscopy revealed that these pores were connected to ciliated invaginations that occasionally contained bacteria. During mid development, these epithelial fields expanded, and separate colonized tubules were observed below the epithelial layer that contained the pores and invaginations. During late development, the superficial epithelial fields appeared to regress as animals approached sexual maturity and were never observed in fully mature adults (about 2-3 months post-hatching), suggesting that they help facilitate bacterial colonization of the accessory nidamental gland. An analysis of 16S rRNA gene diversity in accessory nidamental glands from females of varying size showed that the bacterial community changed as the host approached sexual maturity, increasing in community evenness and shifting from a Verrucomicrobia-dominated to an Alphaproteobacteria-dominated consortium. Given the host's relationship with the well-characterized light organ symbiont Vibrio fischeri, our work suggests that the accessory nidamental gland of E. scolopes may have similar mechanisms to recruit bacteria from the environment. Understanding the developmental and colonization processes of the accessory nidamental gland will expand the use of E. scolopes as a model organism for studying bacterial consortia in marine symbioses.

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来源期刊
Biological Bulletin
Biological Bulletin 生物-海洋与淡水生物学
CiteScore
3.30
自引率
6.20%
发文量
47
审稿时长
6-12 weeks
期刊介绍: The Biological Bulletin disseminates novel scientific results in broadly related fields of biology in keeping with more than 100 years of a tradition of excellence. The Bulletin publishes outstanding original research with an overarching goal of explaining how organisms develop, function, and evolve in their natural environments. To that end, the journal publishes papers in the fields of Neurobiology and Behavior, Physiology and Biomechanics, Ecology and Evolution, Development and Reproduction, Cell Biology, Symbiosis and Systematics. The Bulletin emphasizes basic research on marine model systems but includes articles of an interdisciplinary nature when appropriate.
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