Michael J. Boucher, Sanjita Banerjee, Meenakshi B. Joshi, Angela L. Wei, Matthew J. Nalley, Manning Y. Huang, Susan Lei, Massimiliano Ciranni, Andrew Condon, Andreas Langen, Thomas D. Goddard, Ippolito Caradonna, Alexi I. Goranov, Christina M. Homer, Yasaman Mortensen, Sarah Petnic, Morgann C. Reilly, Ying Xiong, Katherine J. Susa, Vito Paolo Pastore, Hiten D. Madhani
{"title":"一种侵袭性真菌病原体的表型景观揭示了其独特的生物学特性","authors":"Michael J. Boucher, Sanjita Banerjee, Meenakshi B. Joshi, Angela L. Wei, Matthew J. Nalley, Manning Y. Huang, Susan Lei, Massimiliano Ciranni, Andrew Condon, Andreas Langen, Thomas D. Goddard, Ippolito Caradonna, Alexi I. Goranov, Christina M. Homer, Yasaman Mortensen, Sarah Petnic, Morgann C. Reilly, Ying Xiong, Katherine J. Susa, Vito Paolo Pastore, Hiten D. Madhani","doi":"10.1016/j.cell.2025.05.017","DOIUrl":null,"url":null,"abstract":"<em>Cryptococcus neoformans</em> is the most common cause of fungal meningitis and the top-ranking WHO fungal priority pathogen. Only distantly related to model fungi, <em>C. neoformans</em> is also a powerful experimental system for exploring conserved eukaryotic mechanisms lost from specialist model yeast lineages. To decipher its biology globally, we constructed 4,328 gene deletions and measured—with exceptional precision—the fitness of each mutant under 141 diverse growth-limiting <em>in vitro</em> conditions and during murine infection. We defined functional modules by clustering genes based on their phenotypic signatures. In-depth studies leveraged these data in two ways. First, we defined and investigated new components of key signaling pathways, which revealed metazoan-like cellular machinery not present in model yeasts. Second, we identified environmental adaptation mechanisms repurposed to promote mammalian virulence by <em>C. neoformans</em>, which lacks a known animal reservoir. Our work provides an unprecedented resource for deciphering a deadly human pathogen.","PeriodicalId":9656,"journal":{"name":"Cell","volume":"173 1","pages":""},"PeriodicalIF":42.5000,"publicationDate":"2025-06-11","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Phenotypic landscape of an invasive fungal pathogen reveals its unique biology\",\"authors\":\"Michael J. Boucher, Sanjita Banerjee, Meenakshi B. Joshi, Angela L. Wei, Matthew J. Nalley, Manning Y. Huang, Susan Lei, Massimiliano Ciranni, Andrew Condon, Andreas Langen, Thomas D. Goddard, Ippolito Caradonna, Alexi I. Goranov, Christina M. Homer, Yasaman Mortensen, Sarah Petnic, Morgann C. Reilly, Ying Xiong, Katherine J. Susa, Vito Paolo Pastore, Hiten D. Madhani\",\"doi\":\"10.1016/j.cell.2025.05.017\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<em>Cryptococcus neoformans</em> is the most common cause of fungal meningitis and the top-ranking WHO fungal priority pathogen. Only distantly related to model fungi, <em>C. neoformans</em> is also a powerful experimental system for exploring conserved eukaryotic mechanisms lost from specialist model yeast lineages. To decipher its biology globally, we constructed 4,328 gene deletions and measured—with exceptional precision—the fitness of each mutant under 141 diverse growth-limiting <em>in vitro</em> conditions and during murine infection. We defined functional modules by clustering genes based on their phenotypic signatures. In-depth studies leveraged these data in two ways. First, we defined and investigated new components of key signaling pathways, which revealed metazoan-like cellular machinery not present in model yeasts. Second, we identified environmental adaptation mechanisms repurposed to promote mammalian virulence by <em>C. neoformans</em>, which lacks a known animal reservoir. Our work provides an unprecedented resource for deciphering a deadly human pathogen.\",\"PeriodicalId\":9656,\"journal\":{\"name\":\"Cell\",\"volume\":\"173 1\",\"pages\":\"\"},\"PeriodicalIF\":42.5000,\"publicationDate\":\"2025-06-11\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Cell\",\"FirstCategoryId\":\"99\",\"ListUrlMain\":\"https://doi.org/10.1016/j.cell.2025.05.017\",\"RegionNum\":1,\"RegionCategory\":\"生物学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q1\",\"JCRName\":\"BIOCHEMISTRY & MOLECULAR BIOLOGY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Cell","FirstCategoryId":"99","ListUrlMain":"https://doi.org/10.1016/j.cell.2025.05.017","RegionNum":1,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"BIOCHEMISTRY & MOLECULAR BIOLOGY","Score":null,"Total":0}
Phenotypic landscape of an invasive fungal pathogen reveals its unique biology
Cryptococcus neoformans is the most common cause of fungal meningitis and the top-ranking WHO fungal priority pathogen. Only distantly related to model fungi, C. neoformans is also a powerful experimental system for exploring conserved eukaryotic mechanisms lost from specialist model yeast lineages. To decipher its biology globally, we constructed 4,328 gene deletions and measured—with exceptional precision—the fitness of each mutant under 141 diverse growth-limiting in vitro conditions and during murine infection. We defined functional modules by clustering genes based on their phenotypic signatures. In-depth studies leveraged these data in two ways. First, we defined and investigated new components of key signaling pathways, which revealed metazoan-like cellular machinery not present in model yeasts. Second, we identified environmental adaptation mechanisms repurposed to promote mammalian virulence by C. neoformans, which lacks a known animal reservoir. Our work provides an unprecedented resource for deciphering a deadly human pathogen.
期刊介绍:
Cells is an international, peer-reviewed, open access journal that focuses on cell biology, molecular biology, and biophysics. It is affiliated with several societies, including the Spanish Society for Biochemistry and Molecular Biology (SEBBM), Nordic Autophagy Society (NAS), Spanish Society of Hematology and Hemotherapy (SEHH), and Society for Regenerative Medicine (Russian Federation) (RPO).
The journal publishes research findings of significant importance in various areas of experimental biology, such as cell biology, molecular biology, neuroscience, immunology, virology, microbiology, cancer, human genetics, systems biology, signaling, and disease mechanisms and therapeutics. The primary criterion for considering papers is whether the results contribute to significant conceptual advances or raise thought-provoking questions and hypotheses related to interesting and important biological inquiries.
In addition to primary research articles presented in four formats, Cells also features review and opinion articles in its "leading edge" section, discussing recent research advancements and topics of interest to its wide readership.