Unravelling Intrinsic and Extrinsic Factors Shaping the Rich Communities on Lizard Skin

IF 2.7 4区 生物学 Q2 ENVIRONMENTAL SCIENCES
Chava L. Weitzman, Kimberley Day, Karen Gibb, Gregory P. Brown, Angga Rachmansah, Keith Christian
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Abstract

Geckos have high skin bacterial diversity, even though gecko skin has antimicrobial, self-cleaning properties. To gain a better understanding of environment–animal–microbiome interactions in these reptiles, we investigated skin bacteria on seven northern Australian gecko species from five sites and two seasons (n = 234) and found support for our hypotheses of divergent communities between species, sites and seasons. Despite that support, predictor variables had low explanatory power, which increased when focusing within a site or species, explaining up to 40% and 27% of the variation among samples at a site or on a species found in multiple sites, respectively. Weather explained even less variation, as temperature and rainfall did not account for site and season differences. Low explanatory power of these variables indicates that additional factors, or stochasticity, explain much of the bacterial assemblage on geckos. Next, research is needed to determine if these low-biomass communities represent living symbionts. If so, assessing functional similarities, rather than taxonomic profiling, would clarify if bacterial communities have interactive roles with gecko hosts or represent short-lived environmental hitch-hikers and relic DNA.

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揭示塑造蜥蜴皮肤上丰富群落的内在和外在因素。
壁虎的皮肤细菌多样性很高,尽管壁虎的皮肤具有抗菌、自清洁的特性。为了更好地了解这些爬行动物中环境-动物-微生物组的相互作用,我们研究了来自五个地点和两个季节(n = 234)的七种北澳大利亚壁虎物种的皮肤细菌,并发现支持我们的假设,即物种,地点和季节之间存在不同的群落。尽管有这种支持,但预测变量的解释力较低,当集中在一个地点或物种内时,解释力增加,分别解释一个地点或多个地点发现的物种样本之间的差异高达40%和27%。天气对变化的解释更少,因为温度和降雨量不能解释地点和季节的差异。这些变量的低解释力表明,其他因素,或随机性,解释了壁虎上的细菌组合。下一步,需要研究确定这些低生物量群落是否代表活着的共生体。如果是这样,评估功能相似性,而不是分类分析,将澄清细菌群落是否与壁虎宿主有互动作用,还是代表了短暂的环境搭便车者和遗迹DNA。
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来源期刊
Environmental Microbiology Reports
Environmental Microbiology Reports ENVIRONMENTAL SCIENCES-MICROBIOLOGY
CiteScore
6.00
自引率
3.00%
发文量
91
审稿时长
3.0 months
期刊介绍: The journal is identical in scope to Environmental Microbiology, shares the same editorial team and submission site, and will apply the same high level acceptance criteria. The two journals will be mutually supportive and evolve side-by-side. Environmental Microbiology Reports provides a high profile vehicle for publication of the most innovative, original and rigorous research in the field. The scope of the Journal encompasses the diversity of current research on microbial processes in the environment, microbial communities, interactions and evolution and includes, but is not limited to, the following: the structure, activities and communal behaviour of microbial communities microbial community genetics and evolutionary processes microbial symbioses, microbial interactions and interactions with plants, animals and abiotic factors microbes in the tree of life, microbial diversification and evolution population biology and clonal structure microbial metabolic and structural diversity microbial physiology, growth and survival microbes and surfaces, adhesion and biofouling responses to environmental signals and stress factors modelling and theory development pollution microbiology extremophiles and life in extreme and unusual little-explored habitats element cycles and biogeochemical processes, primary and secondary production microbes in a changing world, microbially-influenced global changes evolution and diversity of archaeal and bacterial viruses new technological developments in microbial ecology and evolution, in particular for the study of activities of microbial communities, non-culturable microorganisms and emerging pathogens.
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