Occurrence of fungi in combs of fungus-growing termites (Isoptera: Termitidae, Macrotermitinae)

Herbert J. Guedegbe , Edouard Miambi , Anne Pando , Jocelyne Roman , Pascal Houngnandan , Corinne Rouland-Lefevre
{"title":"Occurrence of fungi in combs of fungus-growing termites (Isoptera: Termitidae, Macrotermitinae)","authors":"Herbert J. Guedegbe ,&nbsp;Edouard Miambi ,&nbsp;Anne Pando ,&nbsp;Jocelyne Roman ,&nbsp;Pascal Houngnandan ,&nbsp;Corinne Rouland-Lefevre","doi":"10.1016/j.mycres.2009.06.008","DOIUrl":null,"url":null,"abstract":"<div><p>Fungus-growing termites cultivate their mutualistic basidiomycete <em>Termitomyces</em> species on a substrate called a fungal comb. Here, the Suicide Polymerase Endonuclease Restriction (SuPER) method was adapted for the first time to a fungal study to determine the entire fungal community of fungal combs and to test whether fungi other than the symbiotic cultivar interact with termite hosts. Our molecular analyses show that although active combs are dominated by <em>Termitomyces</em> fungi isolated with direct Polymerase Endonuclease Restriction – Denaturing Gradient Gel Electrophoresis (PCR-DGGE), they can also harbor some filamentous fungi and yeasts only revealed by SuPER PCR-DGGE. This is the first molecular evidence of the presence of non-<em>Termitomyces</em> species in active combs. However, because there is no evidence for a species-specific relationship between these fungi and termites, they are mere transient guests with no specialization in the symbiosis. It is however surprising to notice that termite-associated <em>Xylaria</em> strains were not isolated from active combs even though they are frequently retrieved when nests are abandoned by termites. This finding highlights the implication of fungus-growing termites in the regulation of fungi occurring within the combs and also suggests that they might not have any particular evolutionary-based association with <em>Xylaria</em> species.</p></div>","PeriodicalId":19045,"journal":{"name":"Mycological research","volume":null,"pages":null},"PeriodicalIF":0.0000,"publicationDate":"2009-10-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1016/j.mycres.2009.06.008","citationCount":"20","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Mycological research","FirstCategoryId":"1085","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S095375620900104X","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 20

Abstract

Fungus-growing termites cultivate their mutualistic basidiomycete Termitomyces species on a substrate called a fungal comb. Here, the Suicide Polymerase Endonuclease Restriction (SuPER) method was adapted for the first time to a fungal study to determine the entire fungal community of fungal combs and to test whether fungi other than the symbiotic cultivar interact with termite hosts. Our molecular analyses show that although active combs are dominated by Termitomyces fungi isolated with direct Polymerase Endonuclease Restriction – Denaturing Gradient Gel Electrophoresis (PCR-DGGE), they can also harbor some filamentous fungi and yeasts only revealed by SuPER PCR-DGGE. This is the first molecular evidence of the presence of non-Termitomyces species in active combs. However, because there is no evidence for a species-specific relationship between these fungi and termites, they are mere transient guests with no specialization in the symbiosis. It is however surprising to notice that termite-associated Xylaria strains were not isolated from active combs even though they are frequently retrieved when nests are abandoned by termites. This finding highlights the implication of fungus-growing termites in the regulation of fungi occurring within the combs and also suggests that they might not have any particular evolutionary-based association with Xylaria species.

查看原文
分享 分享
微信好友 朋友圈 QQ好友 复制链接
本刊更多论文
食真菌白蚁巢内真菌的发生(等翅目:白蚁科,大白蚁科)
生长真菌的白蚁在一种叫做真菌梳的基质上培养它们共生的担子菌白蚁。本研究首次将自杀聚合酶内切酶限制(SuPER)方法应用于真菌研究,以确定真菌梳的整个真菌群落,并测试除共生品种外的真菌是否与白蚁宿主相互作用。我们的分子分析表明,虽然活性梳子以直接聚合酶内切酶-变性梯度凝胶电泳(PCR-DGGE)分离的白蚁真菌为主,但它们也可以容纳一些丝状真菌和酵母,这些真菌只有通过超级PCR-DGGE才能发现。这是在活跃的蜂巢中首次发现非白蚁菌存在的分子证据。然而,由于没有证据表明这些真菌和白蚁之间存在物种特异性关系,它们只是短暂的客人,在共生关系中没有专门化。然而,令人惊讶的是,白蚁相关的木耳菌株并没有从活跃的蜂巢中分离出来,即使它们经常在白蚁遗弃巢穴时被取回。这一发现强调了真菌生长的白蚁对梳子内真菌发生的调节的含义,也表明它们可能与木蝇物种没有任何特定的进化基础联系。
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 去求助
来源期刊
自引率
0.00%
发文量
0
期刊最新文献
Editorial Board Identification of heavy metal regulated genes from the root associated ascomycete Cadophora finlandica using a genomic microarray Molecular and ultrastructural characterization of two ascomycetes found on sunken wood off Vanuatu Islands in the deep Pacific Ocean Trichoderma species form endophytic associations within Theobroma cacao trichomes A beauvericin hot spot in the genus Isaria
×
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
现在去查看 取消
×
提示
确定
0
微信
客服QQ
Book学术公众号 扫码关注我们
反馈
×
意见反馈
请填写您的意见或建议
请填写您的手机或邮箱
已复制链接
已复制链接
快去分享给好友吧!
我知道了
×
扫码分享
扫码分享
Book学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术
文献互助 智能选刊 最新文献 互助须知 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 Book学术 All rights reserved.
ghs 京公网安备 11010802042870号 京ICP备2023020795号-1