北美平原多孢菌属新成员Pleoardoris graminearum, gen. et sp. nov.及其生物地理特征及其对基础禾本科的影响。

IF 2.6 2区 生物学 Q2 MYCOLOGY Mycologia Pub Date : 2023-11-01 Epub Date: 2023-11-14 DOI:10.1080/00275514.2023.2258269
Xiomy-Janiria Pinchi-Davila, Diana Vargas-Hernández, María-José Romero-Jiménez, Ari Jumpponen, Jennifer A Rudgers, Jose Herrera, Miriam Hutchinson, John M Dunbar, Cheryl Kuske, Andrea Porras-Alfaro
{"title":"北美平原多孢菌属新成员Pleoardoris graminearum, gen. et sp. nov.及其生物地理特征及其对基础禾本科的影响。","authors":"Xiomy-Janiria Pinchi-Davila, Diana Vargas-Hernández, María-José Romero-Jiménez, Ari Jumpponen, Jennifer A Rudgers, Jose Herrera, Miriam Hutchinson, John M Dunbar, Cheryl Kuske, Andrea Porras-Alfaro","doi":"10.1080/00275514.2023.2258269","DOIUrl":null,"url":null,"abstract":"<p><p>Diverse fungi colonize plant roots worldwide and include species from many orders of the phylum Ascomycota. These fungi include taxa with dark septate hyphae that colonize grass roots and may modulate plant responses to stress. We describe a novel group of fungal isolates and evaluate their effects on the grass <i>Bouteloua gracilis</i> in vitro. We isolated fungi from roots of six native grasses from 24 sites spanning replicated latitudinal gradients in the south-central US grasslands and characterized isolates phylogenetically using a genome analysis. We analyzed 14 isolates representing a novel clade within the family Montagnulaceae (order Pleosporales), here typified as <i>Pleoardoris graminearum</i>, closely related to the genera <i>Didymocrea</i> and <i>Bimuria</i>. This novel species produces asexual, light brown pycnidium-like conidioma, hyaline hyphae, and chlamydospores when cultured on quinoa and kiwicha agar. To evaluate its effects on <i>B. gracilis</i>, seeds were inoculated with one of three isolates (DS304, DS334, and DS1613) and incubated at 25 C for 20 d. We also tested the effect of volatile organic compounds (VOCs) produced by the same isolates on <i>B. gracilis</i> root and stem lengths. Isolates had variable effects on plant growth. One isolate increased <i>B. gracilis</i> root length up to 34% compared with uninoculated controls. VOCs produced by two isolates increased root and stem lengths (<i>P</i> < 0.05) compared with controls. Internal transcribed spacer ITS2 metabarcode data revealed that <i>P. graminearum</i> is distributed across a wide range of sites in North America (22 of 24 sites sampled), and its relative abundance is influenced by host species identity and latitude. Host species identity and site were the most important factors determining <i>P. graminearum</i> relative abundance in drought experiments at the Extreme Drought in the Grasslands Experiment (EDGE) sites. Variable responses of <i>B. gracilis</i> to inoculation highlight the potential importance of nonmycorrhizal root-associated fungi on plant survival in arid ecosystems.</p>","PeriodicalId":18779,"journal":{"name":"Mycologia","volume":" ","pages":"749-767"},"PeriodicalIF":2.6000,"publicationDate":"2023-11-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"<i>Pleoardoris graminearum</i>, gen. et sp. nov., a new member of Pleosporales from North American Plains, its biogeography and effects on a foundation grass species.\",\"authors\":\"Xiomy-Janiria Pinchi-Davila, Diana Vargas-Hernández, María-José Romero-Jiménez, Ari Jumpponen, Jennifer A Rudgers, Jose Herrera, Miriam Hutchinson, John M Dunbar, Cheryl Kuske, Andrea Porras-Alfaro\",\"doi\":\"10.1080/00275514.2023.2258269\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><p>Diverse fungi colonize plant roots worldwide and include species from many orders of the phylum Ascomycota. These fungi include taxa with dark septate hyphae that colonize grass roots and may modulate plant responses to stress. We describe a novel group of fungal isolates and evaluate their effects on the grass <i>Bouteloua gracilis</i> in vitro. We isolated fungi from roots of six native grasses from 24 sites spanning replicated latitudinal gradients in the south-central US grasslands and characterized isolates phylogenetically using a genome analysis. We analyzed 14 isolates representing a novel clade within the family Montagnulaceae (order Pleosporales), here typified as <i>Pleoardoris graminearum</i>, closely related to the genera <i>Didymocrea</i> and <i>Bimuria</i>. This novel species produces asexual, light brown pycnidium-like conidioma, hyaline hyphae, and chlamydospores when cultured on quinoa and kiwicha agar. To evaluate its effects on <i>B. gracilis</i>, seeds were inoculated with one of three isolates (DS304, DS334, and DS1613) and incubated at 25 C for 20 d. We also tested the effect of volatile organic compounds (VOCs) produced by the same isolates on <i>B. gracilis</i> root and stem lengths. Isolates had variable effects on plant growth. One isolate increased <i>B. gracilis</i> root length up to 34% compared with uninoculated controls. VOCs produced by two isolates increased root and stem lengths (<i>P</i> < 0.05) compared with controls. Internal transcribed spacer ITS2 metabarcode data revealed that <i>P. graminearum</i> is distributed across a wide range of sites in North America (22 of 24 sites sampled), and its relative abundance is influenced by host species identity and latitude. Host species identity and site were the most important factors determining <i>P. graminearum</i> relative abundance in drought experiments at the Extreme Drought in the Grasslands Experiment (EDGE) sites. Variable responses of <i>B. gracilis</i> to inoculation highlight the potential importance of nonmycorrhizal root-associated fungi on plant survival in arid ecosystems.</p>\",\"PeriodicalId\":18779,\"journal\":{\"name\":\"Mycologia\",\"volume\":\" \",\"pages\":\"749-767\"},\"PeriodicalIF\":2.6000,\"publicationDate\":\"2023-11-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Mycologia\",\"FirstCategoryId\":\"99\",\"ListUrlMain\":\"https://doi.org/10.1080/00275514.2023.2258269\",\"RegionNum\":2,\"RegionCategory\":\"生物学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"2023/11/14 0:00:00\",\"PubModel\":\"Epub\",\"JCR\":\"Q2\",\"JCRName\":\"MYCOLOGY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Mycologia","FirstCategoryId":"99","ListUrlMain":"https://doi.org/10.1080/00275514.2023.2258269","RegionNum":2,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2023/11/14 0:00:00","PubModel":"Epub","JCR":"Q2","JCRName":"MYCOLOGY","Score":null,"Total":0}
引用次数: 0

摘要

多样的真菌在世界各地的植物根部定居,包括子囊菌门的许多目的物种。这些真菌包括具有深色分隔菌丝的类群,这些菌丝定殖在草根上,并可能调节植物对胁迫的反应。我们描述了一组新的真菌分离株,并评价了它们对薄叶精品草的体外作用。我们从美国中南部草原上跨越复制纬度梯度的24个地点的6种本地草的根中分离出真菌,并使用基因组分析对分离株进行系统发育表征。我们分析了代表Montagnolaceae(Pleosporales目)中一个新分支的14个分离株,这里的代表是Pleoardoris graminearum,与Didymocrea属和Bimuria属密切相关。当在藜麦和基维查琼脂上培养时,这种新物种会产生无性的浅棕色锥状分生孢子、透明菌丝和厚垣孢子。为了评估其对薄叶B.gracilis的影响,用三个分离株(DS304、DS334和DS1613)中的一个接种种子,并在25℃下培养20天。我们还测试了由相同分离株产生的挥发性有机化合物(VOC)对薄叶B.根和茎长度的影响。分离物对植物生长有不同的影响。与未接种的对照组相比,一个分离株将薄薄叶B.gracilis根的长度增加了34%。与对照组相比,两个分离株产生的VOCs增加了根和茎的长度(P<0.05)。内部转录间隔区ITS2代谢条形码数据显示,禾本科分布在北美的广泛地点(采样的24个地点中有22个),其相对丰度受宿主物种身份和纬度的影响。在极端干旱草地试验(EDGE)场地的干旱试验中,寄主物种身份和地点是决定禾本科相对丰度的最重要因素。薄叶B.gracilis对接种的可变反应突出了非菌根根相关真菌对干旱生态系统中植物生存的潜在重要性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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
Pleoardoris graminearum, gen. et sp. nov., a new member of Pleosporales from North American Plains, its biogeography and effects on a foundation grass species.

Diverse fungi colonize plant roots worldwide and include species from many orders of the phylum Ascomycota. These fungi include taxa with dark septate hyphae that colonize grass roots and may modulate plant responses to stress. We describe a novel group of fungal isolates and evaluate their effects on the grass Bouteloua gracilis in vitro. We isolated fungi from roots of six native grasses from 24 sites spanning replicated latitudinal gradients in the south-central US grasslands and characterized isolates phylogenetically using a genome analysis. We analyzed 14 isolates representing a novel clade within the family Montagnulaceae (order Pleosporales), here typified as Pleoardoris graminearum, closely related to the genera Didymocrea and Bimuria. This novel species produces asexual, light brown pycnidium-like conidioma, hyaline hyphae, and chlamydospores when cultured on quinoa and kiwicha agar. To evaluate its effects on B. gracilis, seeds were inoculated with one of three isolates (DS304, DS334, and DS1613) and incubated at 25 C for 20 d. We also tested the effect of volatile organic compounds (VOCs) produced by the same isolates on B. gracilis root and stem lengths. Isolates had variable effects on plant growth. One isolate increased B. gracilis root length up to 34% compared with uninoculated controls. VOCs produced by two isolates increased root and stem lengths (P < 0.05) compared with controls. Internal transcribed spacer ITS2 metabarcode data revealed that P. graminearum is distributed across a wide range of sites in North America (22 of 24 sites sampled), and its relative abundance is influenced by host species identity and latitude. Host species identity and site were the most important factors determining P. graminearum relative abundance in drought experiments at the Extreme Drought in the Grasslands Experiment (EDGE) sites. Variable responses of B. gracilis to inoculation highlight the potential importance of nonmycorrhizal root-associated fungi on plant survival in arid ecosystems.

求助全文
通过发布文献求助,成功后即可免费获取论文全文。 去求助
来源期刊
Mycologia
Mycologia 生物-真菌学
CiteScore
6.20
自引率
3.60%
发文量
56
审稿时长
4-8 weeks
期刊介绍: International in coverage, Mycologia presents recent advances in mycology, emphasizing all aspects of the biology of Fungi and fungus-like organisms, including Lichens, Oomycetes and Slime Molds. The Journal emphasizes subjects including applied biology, biochemistry, cell biology, development, ecology, evolution, genetics, genomics, molecular biology, morphology, new techniques, animal or plant pathology, phylogenetics, physiology, aspects of secondary metabolism, systematics, and ultrastructure. In addition to research articles, reviews and short notes, Mycologia also includes invited papers based on presentations from the Annual Conference of the Mycological Society of America, such as Karling Lectures or Presidential Addresses.
期刊最新文献
Cell morphological plasticity in response to substrate availability of a cosmopolitan polymorphic yeast from the open ocean. Genome sequencing, phylogenomics, and population analyses of Tilletia, with recognition of one common bunt species, T. caries (synonym T. laevis), distinct from dwarf bunt, T. controversa. The biosynthesis and impacts of cytokinins on growth of the oyster mushroom, Pleurotus ostreatus. Morphology, phylogeny, and mitogenomics reveal a new entomopathogenic fungus, Blackwellomyces changningensis (Hypocreales, Clavicipitaceae), from southwestern China. A new species of Diacheopsis (Myxomycetes) and a new habitat for myxomycetes.
×
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