Constitutive and activated toxigenic activity of Halomicronema metazoicum (Cyanoprokaryota, Cyanophyta)

IF 1.5 4区 生物学 Q3 MARINE & FRESHWATER BIOLOGY
Mirko Mutalipassi, Valerio Mazzella, Francesca Glaviano, Valerio Zupo
{"title":"Constitutive and activated toxigenic activity of Halomicronema metazoicum (Cyanoprokaryota, Cyanophyta)","authors":"Mirko Mutalipassi,&nbsp;Valerio Mazzella,&nbsp;Francesca Glaviano,&nbsp;Valerio Zupo","doi":"10.1111/maec.12697","DOIUrl":null,"url":null,"abstract":"<p><i>Phormidium</i>-like cyanobacteria produce a variety of biologically active molecules. We isolated a free-living strain of <i>Halomicronema metazoicum</i>, previously known uniquely as a symbiont of marine sponges, and demonstrated that its spent medium was toxic for various protozoans and fish parasites. However, we still ignore if its mats contain constitutive or activated defences influencing the physiology of other organisms, with potential influences on organisms that share the same environment. The goal of this study is to clarify if <i>Phormidium</i>-like cyanobacteria accumulate toxic bioactive molecules in the colony tissues, for example for anti-grazing purposes, or if they constitutively secrete them in the medium, with a potential allelopathic function. To address this hypothesis, the toxigenic power of cyanobacterial spent medium and of disintegrated cells (to simulate lysis) was assayed using standard toxicity-tests on nauplii of the brine shrimp <i>Artemia salina</i>. Toxigenic effects were triggered by the spent culture medium, but the homogenates (disintegrated cyanobacteria cells) did not show any acute toxicity. In addition, chronic toxicity tests of the spent medium demonstrated a reduced but still present toxigenic effect, with an inverse correlation between toxicity and medium dilution. The present research contributes to the understanding of cyanobacteria chemical-ecology and shows that they may play fundamental ecological roles, influencing the survival and the blooms of various co-habiting species by constitutively releasing toxic exudates. Since the bioactive compounds produced by <i>H</i>. <i>metazoicum</i> are stable in water, and considering the bioactivity of exudates on invertebrates' physiology, our results might be exploited for the development of novel biotechnologies in the fields of aquaculture, ecological conservation and medicine, due to the potential antitumoral and anti-parasitic activity demonstrated in strictly related species.</p>","PeriodicalId":49883,"journal":{"name":"Marine Ecology-An Evolutionary Perspective","volume":"43 6","pages":""},"PeriodicalIF":1.5000,"publicationDate":"2022-01-20","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"3","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Marine Ecology-An Evolutionary Perspective","FirstCategoryId":"99","ListUrlMain":"https://onlinelibrary.wiley.com/doi/10.1111/maec.12697","RegionNum":4,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q3","JCRName":"MARINE & FRESHWATER BIOLOGY","Score":null,"Total":0}
引用次数: 3

Abstract

Phormidium-like cyanobacteria produce a variety of biologically active molecules. We isolated a free-living strain of Halomicronema metazoicum, previously known uniquely as a symbiont of marine sponges, and demonstrated that its spent medium was toxic for various protozoans and fish parasites. However, we still ignore if its mats contain constitutive or activated defences influencing the physiology of other organisms, with potential influences on organisms that share the same environment. The goal of this study is to clarify if Phormidium-like cyanobacteria accumulate toxic bioactive molecules in the colony tissues, for example for anti-grazing purposes, or if they constitutively secrete them in the medium, with a potential allelopathic function. To address this hypothesis, the toxigenic power of cyanobacterial spent medium and of disintegrated cells (to simulate lysis) was assayed using standard toxicity-tests on nauplii of the brine shrimp Artemia salina. Toxigenic effects were triggered by the spent culture medium, but the homogenates (disintegrated cyanobacteria cells) did not show any acute toxicity. In addition, chronic toxicity tests of the spent medium demonstrated a reduced but still present toxigenic effect, with an inverse correlation between toxicity and medium dilution. The present research contributes to the understanding of cyanobacteria chemical-ecology and shows that they may play fundamental ecological roles, influencing the survival and the blooms of various co-habiting species by constitutively releasing toxic exudates. Since the bioactive compounds produced by Hmetazoicum are stable in water, and considering the bioactivity of exudates on invertebrates' physiology, our results might be exploited for the development of novel biotechnologies in the fields of aquaculture, ecological conservation and medicine, due to the potential antitumoral and anti-parasitic activity demonstrated in strictly related species.

后生褐藻(cyananoprokaryota, Cyanophyta)的组成和激活的产毒活性
类磷蓝藻产生多种生物活性分子。我们分离了一种自由生活的Halomicronema metazoicum菌株,以前被认为是海洋海绵的共生体,并证明了它的废培养基对各种原生动物和鱼类寄生虫是有毒的。然而,我们仍然忽略了它的垫是否含有影响其他生物体生理的构成或激活防御,对共享同一环境的生物体具有潜在的影响。本研究的目的是澄清是否类磷蓝藻在菌落组织中积累有毒的生物活性分子,例如用于抗放牧目的,或者它们是否在培养基中组成性地分泌它们,具有潜在的化感作用。为了验证这一假设,采用标准的盐水对虾(Artemia salina)的nauplii毒性测试,对蓝藻废培养基和分解细胞(模拟裂解)的产毒能力进行了分析。用过的培养基触发了产毒效应,但匀浆(分解的蓝藻细胞)没有表现出任何急性毒性。此外,废培养基的慢性毒性试验表明,毒性与培养基稀释度呈负相关,但仍存在毒性作用。本研究有助于了解蓝藻的化学生态学,并表明它们可能具有基本的生态作用,通过组成性地释放有毒渗出物来影响各种共生物种的生存和繁殖。由于回生弧菌产生的生物活性物质在水中稳定,并且考虑到其分泌物对无脊椎动物生理的生物活性,我们的研究结果可能用于水产养殖、生态保护和医学领域的新生物技术的开发,因为在严格相关的物种中显示出潜在的抗肿瘤和抗寄生虫活性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 求助全文
来源期刊
Marine Ecology-An Evolutionary Perspective
Marine Ecology-An Evolutionary Perspective 生物-海洋与淡水生物学
CiteScore
2.70
自引率
0.00%
发文量
37
审稿时长
>12 weeks
期刊介绍: Marine Ecology publishes original contributions on the structure and dynamics of marine benthic and pelagic ecosystems, communities and populations, and on the critical links between ecology and the evolution of marine organisms. The journal prioritizes contributions elucidating fundamental aspects of species interaction and adaptation to the environment through integration of information from various organizational levels (molecules to ecosystems) and different disciplines (molecular biology, genetics, biochemistry, physiology, marine biology, natural history, geography, oceanography, palaeontology and modelling) as viewed from an ecological perspective. The journal also focuses on population genetic processes, evolution of life histories, morphological traits and behaviour, historical ecology and biogeography, macro-ecology and seascape ecology, palaeo-ecological reconstruction, and ecological changes due to introduction of new biota, human pressure or environmental change. Most applied marine science, including fisheries biology, aquaculture, natural-products chemistry, toxicology, and local pollution studies lie outside the scope of the journal. Papers should address ecological questions that would be of interest to a worldwide readership of ecologists; papers of mostly local interest, including descriptions of flora and fauna, taxonomic descriptions, and range extensions will not be considered.
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术官方微信