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中国真菌学杂志 2023, Vol. 18  Issue (4): 301-309.

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贵州地区临床分离近平滑念珠菌复合群分布及其生物膜形成相关基因研究

王顺1, 李红2, 瞿玉洁1, 李婷婷1, 金婷婷2, 胡方芳2, 罗振华1,3,4   

  1. 1. 贵州大学医学院, 贵阳 550000;
    2. 贵州省人民医检验科, 贵阳 550000;
    3. 贵州省人民医院中心实验室, 贵阳 550000;
    4. 贵州省人民医院国家卫生健康委员会肺脏免疫性疾病诊治重点实验室, 贵阳 550000
  • 收稿日期:2023-02-05 出版日期:2023-08-28 发布日期:2023-09-02
  • 通讯作者: 罗振华,E-mail:luo8300@sina.com E-mail:luo8300@sina.com
  • 作者简介:王顺,男(汉族),硕士,初级技师.E-mail:1437200630@qq.com
  • 基金资助:
    贵州省科技计划项目[(2019)2827];国家自然科学基金地区科学基金项目(82260406);贵州省卫生健康委科学技术基金(gzwkj2021-357)

A study on the distribution and the biofilm formation related genes of Candida parapsilosis complex clinically isolated in Guizhou area

WANG Shun1, LI Hong2, QU Yujie1, LI Tingting1, JIN Tingting2, HU Fangfang2, LUO Zhenhua1,3,4   

  1. 1. School of Medicine, Guizhou University, Gui yang 550000, China;
    2. Department of Clinical Laboratory, Guizhou Provincial People's Hospital, Gui yang 550000, China;
    3. Department of Central Laboratory, Guizhou Provincial People's Hospital, Gui yang 550000, China;
    4. NHC Key Laboratory of Pulmonary Immune-related Diseases, Guizhou Provincial People's Hospital, Gui yang 550000, China
  • Received:2023-02-05 Online:2023-08-28 Published:2023-09-02

摘要: 目的 研究贵州地区近平滑念珠菌复合群临床分布和药敏特点,检测近平滑念珠菌生物膜形成能力及其CDC28基因的表达水平。方法 收集贵州地区2所三级甲等医院送检标本中分离出的菌株,利用BACTECTM FX仪、Phoenix-100仪对菌种进行鉴定,通过基因测序对近平滑念珠菌复合群各分型菌株进行鉴定;采用ATB FUNGUS 3试剂盒检测菌株体外药物敏感情况;检测血源性近平滑念珠菌生物膜形成能力及利用qRT-PCR技术检测它们的CDC28基因表达水平。结果 共分离鉴定出163株近平滑念珠菌复合群,其中近平滑念珠菌I型、II型和III型分别占73.0%、6.1%和20.9%;尿液和血液是分离菌株最多的标本(均为50株);血液途径感染的菌株中,I型、II型和 III型分别占54.0%、10.0%和36.0%;三种基因型菌株对常见抗真菌药物无明显耐药性;17株临床菌株中,16株(94.1%)具有生物膜形成能力,其中2株、4株和10株菌株生物膜形成能力强、一般、弱, CDC28在2株生物膜形成能力强以及3株生物膜形成能力一般的菌株中表达上调。结论 分离的近平滑念珠菌复合群以I型感染为主,三种基因型菌株对抗真菌药物无明显耐药性;不同血源性近平滑念珠菌生物膜形成能力不同,CDC28基因与近平滑念珠菌生物膜形成有关。

关键词: 近平滑念珠菌感染, 临床特征, 药物敏感特征, 生物膜形成, 基因表达

Abstract: Objective The distribution of infection and drug susceptibility characteristics of Candida parapsilosis complex strains were studied in Guizhou. Detection of the biofilm formation capacity of strains and the expression level of its CDC28 gene were performed. Methods The BACTECTM FX and Phoenix-100 instrument were used to identify the strains isolated in there tertiary first class hospitals in Guizhou from January 2017 to December 2019. The Candida parapsilosis complex group was identified by gene sequencing. ATB FUNGUS 3 kit was used to detect drug susceptibility of strains. The Candida parapsilosis biofilms formation capacitywas detected, and the expression levels of their CDC28 genes were detected using qRT-PCR. Results A total of 163 strains of Candida parapsilosis complex were isolated and identified, of which Candida parapsilosis type I, II and III accounted for 73.0%, 6.1% and 20.9% respectively. Urine and blood specimens got the most isolated strains (both 50 strains). Among the ioslates from infected bloodstream, type I, II and III accounted for 54.0%, 10.0% and 36.0% respectively. Three genotype strains were not significantly resistant to antifungal drugs. Among the 17 clinical strains, 16 (94.1%) had biofilm formation ability, of which 2, 4 and 10 strains had strong, general and weak biofilm formation capacity. CDC28 expressed upregulation in 2 strains with strong and 3 strains with general ability. Conclusion The isolated Candida parapsilosis complex was dominated by type I, and the three genotype strains were not obviously resistant to antifungal drugs. Different Candida parapsilosis showed different biofilm formation capacity, and the CDC28 gene might be associated with biofilm formation.

Key words: Candida parapsilosis infection, clinical characteristics, drug susceptibility characteristics, biofilm formation, gene expression

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