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
  • [1] Iron acquisition in the human fungal pathogen Cryptococcus neoformans
    Jung, Won Hee
    Do, Eunsoo
    CURRENT OPINION IN MICROBIOLOGY, 2013, 16 (06) : 686 - 691
  • [2] Zinc Finger Proteins in the Human Fungal Pathogen Cryptococcus neoformans
    Li, Yuan-Hong
    Liu, Tong-Bao
    INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES, 2020, 21 (04)
  • [3] Investigation of Antifungal Mechanisms of Thymol in the Human Fungal Pathogen, Cryptococcus neoformans
    Jung, Kwang-Woo
    Chung, Moon-Soo
    Bai, Hyoung-Woo
    Chung, Byung-Yeoup
    Lee, Sungbeom
    MOLECULES, 2021, 26 (11):
  • [4] Phosphatidylserine synthesis is essential for viability of the human fungal pathogen Cryptococcus neoformans
    Konarzewska, Paulina
    Wang, Yina
    Han, Gil-Soo
    Goh, Kwok Jian
    Gao, Yong-Gui
    Carman, George M.
    Xue, Chaoyang
    JOURNAL OF BIOLOGICAL CHEMISTRY, 2019, 294 (07) : 2329 - 2339
  • [5] Proteomic Analysis of Copper Toxicity in Human Fungal Pathogen Cryptococcus neoformans
    Sun, Tianshu
    Li, Yanjian
    Li, Yingxing
    Li, Hailong
    Gong, Yiyi
    Wu, Jianqiang
    Ning, Yating
    Ding, Chen
    Xu, Yingchun
    FRONTIERS IN CELLULAR AND INFECTION MICROBIOLOGY, 2021, 11
  • [6] Elucidating the Pathogenesis of Spores from the Human Fungal Pathogen Cryptococcus neoformans
    Giles, Steven S.
    Dagenais, Taylor R. T.
    Botts, Michael R.
    Keller, Nancy P.
    Hull, Christina M.
    INFECTION AND IMMUNITY, 2009, 77 (08) : 3491 - 3500
  • [7] Systematic functional analysis of kinases in the fungal pathogen Cryptococcus neoformans
    Lee, Kyung-Tae
    So, Yee-Seul
    Yang, Dong-Hoon
    Jung, Kwang-Woo
    Choi, Jaeyoung
    Lee, Dong-Gi
    Kwon, Hyojeong
    Jang, Juyeong
    Wang, Li Li
    Cha, Soohyun
    Meyers, Gena Lee
    Jeong, Eunji
    Jin, Jae-Hyung
    Lee, Yeonseon
    Hong, Joohyeon
    Bang, Soohyun
    Ji, Je-Hyun
    Park, Goun
    Byun, Hyo-Jeong
    Park, Sung Woo
    Park, Young-Min
    Adedoyin, Gloria
    Kim, Taeyup
    Averette, Anna F.
    Choi, Jong-Soon
    Heitman, Joseph
    Cheong, Eunji
    Lee, Yong-Hwan
    Bahn, Yong-Sun
    NATURE COMMUNICATIONS, 2016, 7
  • [8] Genotypic and Phenotypic Analyses of Two "Isogenic" Strains of the Human Fungal Pathogen Cryptococcus neoformans var. neoformans
    Hua, Wenjing
    Vogan, Aaron
    Xu, Jianping
    MYCOPATHOLOGIA, 2019, 184 (02) : 195 - 212
  • [9] The ER stress response and host temperature adaptation in the human fungal pathogen Cryptococcus neoformans
    Glazier, Virginia E.
    Panepinto, John C.
    VIRULENCE, 2014, 5 (02) : 351 - 356
  • [10] Nitrogen Metabolite Repression of Metabolism and Virulence in the Human Fungal Pathogen Cryptococcus neoformans
    Lee, I. Russel
    Chow, Eve W. L.
    Morrow, Carl A.
    Djordjevic, Julianne T.
    Fraser, James A.
    GENETICS, 2011, 188 (02) : 309 - U140