Mixed Infections and In Vivo Evolution in the Human Fungal Pathogen Cryptococcus neoformans

被引:82
|
作者
Desnos-Ollivier, Marie [1 ,2 ]
Patel, Sweta [1 ,2 ]
Spaulding, Adam R. [3 ]
Charlier, Caroline [1 ,2 ]
Garcia-Hermoso, Dea [1 ,2 ]
Nielsen, Kirsten [3 ]
Dromer, Francoise [1 ,2 ]
机构
[1] Inst Pasteur, Mol Mycol Unit, Paris, France
[2] CNRS, URA3012, Paris, France
[3] Univ Minnesota, Sch Med, Dept Microbiol, Minneapolis, MN 55455 USA
来源
MBIO | 2010年 / 1卷 / 01期
基金
美国国家卫生研究院;
关键词
MATING-TYPE LOCUS; CANDIDA-ALBICANS; MOLECULAR EPIDEMIOLOGY; ALPHA-STRAINS; AIDS PATIENTS; SEXUAL CYCLE; VAR; GRUBII; VIRULENCE; SEROTYPE; MICROEVOLUTION;
D O I
10.1128/mBio.00091-10
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Koch's postulates are criteria establishing a causal relationship between a microbe and a disease that lead to the assumption that diseases are caused by a single strain or its evolved forms. Cryptococcus neoformans is a life-threatening human fungal pathogen responsible for an estimated 1 million cases of cryptococcosis/year, predominantly meningoencephalitis. To assess the molecular diversity of clinical isolates and gain knowledge of C. neoformans biology in the host, we analyzed clinical cultures collected during the prospective CryptoA/D study. Using molecular analysis of unpurified isolates, we demonstrated that mixed infections in humans are more common than previously thought, occurring in almost 20% of patients diagnosed with cryptococcosis. These mixed infections are composed of different mating types, serotypes, and/or genotypes. We also identified genetically related haploid and diploid strains in the same patients. Experimental infections and quantitative PCR show that these ploidy changes can result from endoreplication (duplication of DNA content) and that shuttling between haploid and diploid states can occur, suggesting in vivo evolution. Thus, the concept of one strain/one infection does not hold true for C. neoformans and may apply to other environmentally acquired fungal pathogens. Furthermore, the possibility of mixed and/or evolving infections should be taken into account when developing therapeutic strategies against these pathogens. IMPORTANCE Cryptococcus neoformans is a life-threatening human fungal pathogen that is present in the environment and is responsible for an estimated 1 million cases of cryptococcosis/year, predominantly meningoencephalitis in HIV-infected patients. To assess the molecular diversity of clinical isolates and gain knowledge of C. neoformans biology in the host, we analyzed clinical cultures collected during a prospective study on cryptococcosis. Using molecular analysis of unpurified isolates, we uncovered an unexpectedly high frequency (almost 20%) of mixed infections. We further demonstrated that these mixed infections could result from infestation by multiple strains acquired from the environment. We also made the serendipitous discovery of in vivo evolution leading to endoreplication of the yeasts within the host. Thus, the concept of one strain causing one infection does not hold true for C. neoformans and potentially for other environmentally acquired fungal pathogens. The possibility of mixed and/or evolving infections should be taken into account when developing therapeutic strategies against these pathogens.
引用
收藏
页数:9
相关论文
共 50 条
  • [31] Elucidation of the calcineurin-Crz1 stress response transcriptional network in the human fungal pathogen Cryptococcus neoformans
    Chow, Eve W. L.
    Clancey, Shelly A.
    Billmyre, R. Blake
    Averette, Anna Floyd
    Granek, Joshua A.
    Mieczkowski, Piotr
    Cardenas, Maria E.
    Heitman, Joseph
    PLOS GENETICS, 2017, 13 (04):
  • [32] Multiple F-Box Proteins Collectively Regulate Cell Development and Pathogenesis in the Human Pathogen Cryptococcus neoformans
    Cao, Chengjun
    Wang, Yina
    Avina, Samantha L.
    Walter, John
    Xue, Chaoyang
    JOURNAL OF FUNGI, 2022, 8 (12)
  • [33] The TOR Pathway Plays Pleiotropic Roles in Growth and Stress Responses of the Fungal Pathogen Cryptococcus neoformans
    So, Yee-Seul
    Lee, Dong-Gi
    Idnurm, Alexander
    Ianiri, Giuseppe
    Bahn, Yong-Sun
    GENETICS, 2019, 212 (04) : 1241 - 1258
  • [34] Identification of Genes from the Fungal Pathogen Cryptococcus neoformans Related to Transmigration into the Central Nervous System
    Tseng, Hsiang-Kuang
    Liu, Chang-Pan
    Price, Michael S.
    Jong, Ambrose Y.
    Chang, Jui-Chih
    Toffaletti, Dena L.
    Betancourt-Quiroz, Marisol
    Frazzitta, Aubrey E.
    Cho, Wen-Long
    Perfect, John R.
    PLOS ONE, 2012, 7 (09):
  • [35] Congenic Strains of the Filamentous Form of Cryptococcus neoformans for Studies of Fungal Morphogenesis and Virulence
    Zhai, Bing
    Zhu, Pinkuan
    Foyle, Dylan
    Upadhyay, Srijana
    Idnurm, Alexander
    Lin, Xiaorong
    INFECTION AND IMMUNITY, 2013, 81 (07) : 2626 - 2637
  • [36] Role of clathrin-mediated endocytosis in the use of heme and hemoglobin by the fungal pathogen Cryptococcus neoformans
    Bairwa, Gaurav
    Caza, Melissa
    Horianopoulos, Linda
    Hu, Guanggan
    Kronstad, James
    CELLULAR MICROBIOLOGY, 2019, 21 (03)
  • [37] Investigating Conservation of the Cell-Cycle-Regulated Transcriptional Program in the Fungal Pathogen, Cryptococcus neoformans
    Kelliher, Christina M.
    Leman, Adam R.
    Sierra, Crystal S.
    Haase, Steven B.
    PLOS GENETICS, 2016, 12 (12):
  • [38] Intersection of fungal fitness and virulence in Cryptococcus neoformans
    Panepinto, John C.
    Williamson, Peter R.
    FEMS YEAST RESEARCH, 2006, 6 (04) : 489 - 498
  • [39] Unraveling Unique Structure and Biosynthesis Pathway of N-Linked Glycans in Human Fungal Pathogen Cryptococcus neoformans by Glycomics Analysis
    Park, Jeong-Nam
    Lee, Dong-Jik
    Kwon, Ohsuk
    Oh, Doo-Byoung
    Bahn, Yong-Sun
    Kang, Hyun Ah
    JOURNAL OF BIOLOGICAL CHEMISTRY, 2012, 287 (23) : 19501 - 19515
  • [40] Ctr2 Links Copper Homeostasis to Polysaccharide Capsule Formation and Phagocytosis Inhibition in the Human Fungal Pathogen Cryptococcus neoformans
    Chun, Cheryl D.
    Madhani, Hiten D.
    PLOS ONE, 2010, 5 (09): : 1 - 10