D P Wei, E Gentekaki, J J Luangsa-Ard, N N Wijayawardene, D N Wanasinghe, Z L Liu, Q F Huang, N Y Liu, S W Xie, J C Kang, T C Wen
{"title":"亚克雷亚目高寄生虫及其相关昆虫病原体的分类、系统发育和多样性。","authors":"D P Wei, E Gentekaki, J J Luangsa-Ard, N N Wijayawardene, D N Wanasinghe, Z L Liu, Q F Huang, N Y Liu, S W Xie, J C Kang, T C Wen","doi":"10.3114/sim.2026.114.02","DOIUrl":null,"url":null,"abstract":"<p><p>Hyperparasitic fungi associated with hypocrealean entomopathogens play a pivotal yet underexplored role in regulating fungal-arthropod interaction networks. Despite their frequent occurrence in nature, the taxonomic diversity and evolutionary relationships of these hyperparasites remain poorly resolved. In this study, we conducted an integrative taxonomic investigation of hyperparasites associated with hypocrealean entomopathogenic fungi, together with their closely allied entomopathogenic taxa. Multilocus phylogenetic analyses based on LSU, ITS, SSU, <i>tef-1α</i>, <i>rpb1</i>, and <i>rpb2</i> were employed to reconstruct phylogenetic relationships, and molecular clock analyses were conducted independently to infer evolutionary timescales of families within <i>Hypocreales</i>. Morphological examinations were used to corroborate species delimitation and generic circumscription. Our results substantially expand the known diversity of this group, revealing one novel family, <i>Chlorocilliaceae fam. nov.</i>, two new genera (<i>Paralecanicillium gen. nov.</i> and <i>Neodingleyomyces gen. nov.</i>), and 18 new species. In addition, three new combinations, seven new host, geographic, or asexual morph records, and two previously described species are documented, comprising a total of 30 species distributed across 18 genera and six families. <i>Chlorocilliaceae</i> is proposed to accommodate <i>Albacillium</i>, <i>Chlorocillium</i>, <i>Fiorinimazzantia</i>, <i>Husseyia</i>, <i>Neoaraneomyces</i>, <i>Paraneoaraneomyces</i>, <i>Rousseaua</i>, <i>Speluncomyces</i> and <i>Subuliphorum</i>. Updated descriptions and emended generic concepts of <i>Fiorinimazzantia</i> and <i>Husseyia</i> are provided based on newly collected material. This study advances our understanding of the taxonomy, evolutionary history, and hidden diversity of hyperparasitic fungi allied to hypocrealean entomopathogens, and provides a robust framework for elucidating tripartite host-pathogen-hyperparasite interactions in fungal ecology. <b>Taxonomic novelties: New family:</b> <i>Chlorocilliaceae</i> D.P. Wei & T.C. Wen. <b>New genera:</b> <i>Neodingleyomyces</i> D.P. Wei, Z.L. Liu & T.C. Wen, <i>Paralecanicillium</i> D.P. Wei & T.C. Wen. <b>New species:</b> <i>Ascopolyporus sanduensis</i> D.P. Wei & T.C. Wen, <i>Calcarisporium ophiocordycipiticola</i> D.P. Wei & T.C. Wen, <i>Chlorocillium aschersoniae</i> D.P. Wei & T.C. Wen, <i>Chlorocillium coccidiicola</i> D.P. Wei & T.C. Wen, <i>Chlorocillium cordycipiticola</i> D.P. Wei, Z.L. Liu & T.C. Wen, <i>Chlorocillium gibellulae</i> D.P. Wei & T.C. Wen, <i>Chlorocillium globiceps</i> D.P. Wei & T.C. Wen, <i>Chlorocillium houqiaoense</i> D.P. Wei, Q. F. Huang & T.C. Wen, <i>Chlorocillium menghaiense</i> D.P. Wei & T.C. Wen, <i>Chlorocillium puerense</i> D.P. Wei, Z.L. Liu & T.C. Wen, <i>Chlorocillium sanduense</i> D.P. Wei & T.C. Wen, <i>Chlorocillium taiyangheense</i> D.P. Wei & T.C. Wen, <i>Chlorocillium tengchongense</i> D.P. Wei, N.Y. Liu & T.C. Wen, <i>Husseyia ramosissima</i> D.P. Wei & T.C. Wen, <i>Neodingleyomyces tengchongensis</i> D.P. Wei, N.Y. Liu & T.C. Wen, <i>Ophiocordyceps shimenxiaensis</i> D.P. Wei & T.C. Wen, <i>Paralecanicillium yunnanense</i> D.P. Wei & T.C. Wen, <i>Pleurocordyceps simaoensis</i> D.P. Wei & T.C. Wen. <b>New combinations:</b> <i>Calcarisporium andense</i> (Flakus <i>et al.</i>) D.P. Wei & T.C. Wen, <i>Calcarisporium agaricicola</i> (Berk.) D.P. Wei & T.C. Wen, <i>Torrubiellomyces sessilis</i> (Kaitsu <i>et al.</i>) D.P. Wei, T.C. Wen. <b>New records:</b> <i>Albacillium hingganense</i> M.M. Ding & L.J. Xu, <i>Chlorocillium neolepidopterorum</i> (W.H. Chen <i>et al.</i>) W.H. Chen <i>et al.</i>, <i>Fiorinimazzantia elisabettae</i> Y.P. Tan <i>et al.</i>, <i>Pleurocordyceps heilongtanensis</i> Y.B. Wang <i>et al.</i>, <i>Pleurocordyceps parvicapitata</i> Y.P. Xiao <i>et al.</i>, <i>Pleurocordyceps neoagarica</i> Yu Yang & Yuan Pin Xiao, <i>Paradingleyomyces lepidopterorum</i> Y. Wang tris & T.C. Wen. <b>Replacement names:</b> <i>Torrubiellomyces</i> J.P.M. Araújo & de Bekker. <b>Citation:</b> Wei DP, Gentekaki E, Luangsa-ard JJ, Wijayawardene NN, Wanasinghe DN, Liu ZL, Huang QF, Liu NY, Xie SW, Kang JC, Wen TC (2026). Taxonomy, phylogeny and diversity of hyperparasites and their allied entomopathogens in <i>Hypocreales</i>. <i>Studies in Mycology</i> <b>114</b>: 370-436. doi: 10.3114/sim.2026.114.02.</p>","PeriodicalId":22036,"journal":{"name":"Studies in Mycology","volume":"114 ","pages":"370-436"},"PeriodicalIF":18.3000,"publicationDate":"2026-05-20","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC13487413/pdf/","citationCount":"0","resultStr":"{\"title\":\"Taxonomy, phylogeny and diversity of hyperparasites and their allied entomopathogens in <i>Hypocreales</i>.\",\"authors\":\"D P Wei, E Gentekaki, J J Luangsa-Ard, N N Wijayawardene, D N Wanasinghe, Z L Liu, Q F Huang, N Y Liu, S W Xie, J C Kang, T C Wen\",\"doi\":\"10.3114/sim.2026.114.02\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><p>Hyperparasitic fungi associated with hypocrealean entomopathogens play a pivotal yet underexplored role in regulating fungal-arthropod interaction networks. Despite their frequent occurrence in nature, the taxonomic diversity and evolutionary relationships of these hyperparasites remain poorly resolved. In this study, we conducted an integrative taxonomic investigation of hyperparasites associated with hypocrealean entomopathogenic fungi, together with their closely allied entomopathogenic taxa. Multilocus phylogenetic analyses based on LSU, ITS, SSU, <i>tef-1α</i>, <i>rpb1</i>, and <i>rpb2</i> were employed to reconstruct phylogenetic relationships, and molecular clock analyses were conducted independently to infer evolutionary timescales of families within <i>Hypocreales</i>. Morphological examinations were used to corroborate species delimitation and generic circumscription. Our results substantially expand the known diversity of this group, revealing one novel family, <i>Chlorocilliaceae fam. nov.</i>, two new genera (<i>Paralecanicillium gen. nov.</i> and <i>Neodingleyomyces gen. nov.</i>), and 18 new species. In addition, three new combinations, seven new host, geographic, or asexual morph records, and two previously described species are documented, comprising a total of 30 species distributed across 18 genera and six families. <i>Chlorocilliaceae</i> is proposed to accommodate <i>Albacillium</i>, <i>Chlorocillium</i>, <i>Fiorinimazzantia</i>, <i>Husseyia</i>, <i>Neoaraneomyces</i>, <i>Paraneoaraneomyces</i>, <i>Rousseaua</i>, <i>Speluncomyces</i> and <i>Subuliphorum</i>. Updated descriptions and emended generic concepts of <i>Fiorinimazzantia</i> and <i>Husseyia</i> are provided based on newly collected material. This study advances our understanding of the taxonomy, evolutionary history, and hidden diversity of hyperparasitic fungi allied to hypocrealean entomopathogens, and provides a robust framework for elucidating tripartite host-pathogen-hyperparasite interactions in fungal ecology. <b>Taxonomic novelties: New family:</b> <i>Chlorocilliaceae</i> D.P. Wei & T.C. Wen. <b>New genera:</b> <i>Neodingleyomyces</i> D.P. Wei, Z.L. Liu & T.C. Wen, <i>Paralecanicillium</i> D.P. Wei & T.C. Wen. <b>New species:</b> <i>Ascopolyporus sanduensis</i> D.P. Wei & T.C. Wen, <i>Calcarisporium ophiocordycipiticola</i> D.P. Wei & T.C. Wen, <i>Chlorocillium aschersoniae</i> D.P. Wei & T.C. Wen, <i>Chlorocillium coccidiicola</i> D.P. Wei & T.C. Wen, <i>Chlorocillium cordycipiticola</i> D.P. Wei, Z.L. Liu & T.C. Wen, <i>Chlorocillium gibellulae</i> D.P. Wei & T.C. Wen, <i>Chlorocillium globiceps</i> D.P. Wei & T.C. Wen, <i>Chlorocillium houqiaoense</i> D.P. Wei, Q. F. Huang & T.C. Wen, <i>Chlorocillium menghaiense</i> D.P. Wei & T.C. Wen, <i>Chlorocillium puerense</i> D.P. Wei, Z.L. Liu & T.C. Wen, <i>Chlorocillium sanduense</i> D.P. Wei & T.C. Wen, <i>Chlorocillium taiyangheense</i> D.P. Wei & T.C. Wen, <i>Chlorocillium tengchongense</i> D.P. Wei, N.Y. Liu & T.C. Wen, <i>Husseyia ramosissima</i> D.P. Wei & T.C. Wen, <i>Neodingleyomyces tengchongensis</i> D.P. Wei, N.Y. Liu & T.C. Wen, <i>Ophiocordyceps shimenxiaensis</i> D.P. Wei & T.C. Wen, <i>Paralecanicillium yunnanense</i> D.P. Wei & T.C. Wen, <i>Pleurocordyceps simaoensis</i> D.P. Wei & T.C. Wen. <b>New combinations:</b> <i>Calcarisporium andense</i> (Flakus <i>et al.</i>) D.P. Wei & T.C. Wen, <i>Calcarisporium agaricicola</i> (Berk.) D.P. Wei & T.C. Wen, <i>Torrubiellomyces sessilis</i> (Kaitsu <i>et al.</i>) D.P. Wei, T.C. Wen. <b>New records:</b> <i>Albacillium hingganense</i> M.M. Ding & L.J. Xu, <i>Chlorocillium neolepidopterorum</i> (W.H. Chen <i>et al.</i>) W.H. Chen <i>et al.</i>, <i>Fiorinimazzantia elisabettae</i> Y.P. Tan <i>et al.</i>, <i>Pleurocordyceps heilongtanensis</i> Y.B. Wang <i>et al.</i>, <i>Pleurocordyceps parvicapitata</i> Y.P. Xiao <i>et al.</i>, <i>Pleurocordyceps neoagarica</i> Yu Yang & Yuan Pin Xiao, <i>Paradingleyomyces lepidopterorum</i> Y. Wang tris & T.C. Wen. <b>Replacement names:</b> <i>Torrubiellomyces</i> J.P.M. Araújo & de Bekker. <b>Citation:</b> Wei DP, Gentekaki E, Luangsa-ard JJ, Wijayawardene NN, Wanasinghe DN, Liu ZL, Huang QF, Liu NY, Xie SW, Kang JC, Wen TC (2026). Taxonomy, phylogeny and diversity of hyperparasites and their allied entomopathogens in <i>Hypocreales</i>. <i>Studies in Mycology</i> <b>114</b>: 370-436. doi: 10.3114/sim.2026.114.02.</p>\",\"PeriodicalId\":22036,\"journal\":{\"name\":\"Studies in Mycology\",\"volume\":\"114 \",\"pages\":\"370-436\"},\"PeriodicalIF\":18.3000,\"publicationDate\":\"2026-05-20\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC13487413/pdf/\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Studies in Mycology\",\"FirstCategoryId\":\"99\",\"ListUrlMain\":\"https://doi.org/10.3114/sim.2026.114.02\",\"RegionNum\":1,\"RegionCategory\":\"生物学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"2026/6/1 0:00:00\",\"PubModel\":\"eCollection\",\"JCR\":\"Q1\",\"JCRName\":\"MYCOLOGY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Studies in Mycology","FirstCategoryId":"99","ListUrlMain":"https://doi.org/10.3114/sim.2026.114.02","RegionNum":1,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2026/6/1 0:00:00","PubModel":"eCollection","JCR":"Q1","JCRName":"MYCOLOGY","Score":null,"Total":0}
Taxonomy, phylogeny and diversity of hyperparasites and their allied entomopathogens in Hypocreales.
Hyperparasitic fungi associated with hypocrealean entomopathogens play a pivotal yet underexplored role in regulating fungal-arthropod interaction networks. Despite their frequent occurrence in nature, the taxonomic diversity and evolutionary relationships of these hyperparasites remain poorly resolved. In this study, we conducted an integrative taxonomic investigation of hyperparasites associated with hypocrealean entomopathogenic fungi, together with their closely allied entomopathogenic taxa. Multilocus phylogenetic analyses based on LSU, ITS, SSU, tef-1α, rpb1, and rpb2 were employed to reconstruct phylogenetic relationships, and molecular clock analyses were conducted independently to infer evolutionary timescales of families within Hypocreales. Morphological examinations were used to corroborate species delimitation and generic circumscription. Our results substantially expand the known diversity of this group, revealing one novel family, Chlorocilliaceae fam. nov., two new genera (Paralecanicillium gen. nov. and Neodingleyomyces gen. nov.), and 18 new species. In addition, three new combinations, seven new host, geographic, or asexual morph records, and two previously described species are documented, comprising a total of 30 species distributed across 18 genera and six families. Chlorocilliaceae is proposed to accommodate Albacillium, Chlorocillium, Fiorinimazzantia, Husseyia, Neoaraneomyces, Paraneoaraneomyces, Rousseaua, Speluncomyces and Subuliphorum. Updated descriptions and emended generic concepts of Fiorinimazzantia and Husseyia are provided based on newly collected material. This study advances our understanding of the taxonomy, evolutionary history, and hidden diversity of hyperparasitic fungi allied to hypocrealean entomopathogens, and provides a robust framework for elucidating tripartite host-pathogen-hyperparasite interactions in fungal ecology. Taxonomic novelties: New family:Chlorocilliaceae D.P. Wei & T.C. Wen. New genera:Neodingleyomyces D.P. Wei, Z.L. Liu & T.C. Wen, Paralecanicillium D.P. Wei & T.C. Wen. New species:Ascopolyporus sanduensis D.P. Wei & T.C. Wen, Calcarisporium ophiocordycipiticola D.P. Wei & T.C. Wen, Chlorocillium aschersoniae D.P. Wei & T.C. Wen, Chlorocillium coccidiicola D.P. Wei & T.C. Wen, Chlorocillium cordycipiticola D.P. Wei, Z.L. Liu & T.C. Wen, Chlorocillium gibellulae D.P. Wei & T.C. Wen, Chlorocillium globiceps D.P. Wei & T.C. Wen, Chlorocillium houqiaoense D.P. Wei, Q. F. Huang & T.C. Wen, Chlorocillium menghaiense D.P. Wei & T.C. Wen, Chlorocillium puerense D.P. Wei, Z.L. Liu & T.C. Wen, Chlorocillium sanduense D.P. Wei & T.C. Wen, Chlorocillium taiyangheense D.P. Wei & T.C. Wen, Chlorocillium tengchongense D.P. Wei, N.Y. Liu & T.C. Wen, Husseyia ramosissima D.P. Wei & T.C. Wen, Neodingleyomyces tengchongensis D.P. Wei, N.Y. Liu & T.C. Wen, Ophiocordyceps shimenxiaensis D.P. Wei & T.C. Wen, Paralecanicillium yunnanense D.P. Wei & T.C. Wen, Pleurocordyceps simaoensis D.P. Wei & T.C. Wen. New combinations:Calcarisporium andense (Flakus et al.) D.P. Wei & T.C. Wen, Calcarisporium agaricicola (Berk.) D.P. Wei & T.C. Wen, Torrubiellomyces sessilis (Kaitsu et al.) D.P. Wei, T.C. Wen. New records:Albacillium hingganense M.M. Ding & L.J. Xu, Chlorocillium neolepidopterorum (W.H. Chen et al.) W.H. Chen et al., Fiorinimazzantia elisabettae Y.P. Tan et al., Pleurocordyceps heilongtanensis Y.B. Wang et al., Pleurocordyceps parvicapitata Y.P. Xiao et al., Pleurocordyceps neoagarica Yu Yang & Yuan Pin Xiao, Paradingleyomyces lepidopterorum Y. Wang tris & T.C. Wen. Replacement names:Torrubiellomyces J.P.M. Araújo & de Bekker. Citation: Wei DP, Gentekaki E, Luangsa-ard JJ, Wijayawardene NN, Wanasinghe DN, Liu ZL, Huang QF, Liu NY, Xie SW, Kang JC, Wen TC (2026). Taxonomy, phylogeny and diversity of hyperparasites and their allied entomopathogens in Hypocreales. Studies in Mycology114: 370-436. doi: 10.3114/sim.2026.114.02.
期刊介绍:
The international journal Studies in Mycology focuses on advancing the understanding of filamentous fungi, yeasts, and various aspects of mycology. It publishes comprehensive systematic monographs as well as topical issues covering a wide range of subjects including biotechnology, ecology, molecular biology, pathology, and systematics. This Open-Access journal offers unrestricted access to its content.
Each issue of Studies in Mycology consists of around 5 to 6 papers, either in the form of monographs or special focused topics. Unlike traditional length restrictions, the journal encourages submissions of manuscripts with a minimum of 50 A4 pages in print. This ensures a thorough exploration and presentation of the research findings, maximizing the depth of the published work.