Species distribution and antifungal susceptibilities of clinical isolates of Penicillium and Talaromyces species in China

被引:8
作者
Guo, Li-Na [1 ,2 ]
Yu, Shu-Ying [1 ,2 ,3 ]
Wang, Yao [1 ,2 ]
Liu, Ya-Li [1 ,2 ]
Yuan, Ying [1 ,2 ]
Duan, Si-Meng [1 ,2 ]
Yang, Wen-Hang [1 ,2 ,3 ]
Jia, Xin-Miao [4 ]
Zhao, Ying [1 ,2 ]
Xiao, Meng [1 ,2 ]
Xie, Xiu-Li [1 ,2 ]
Dou, Hong-Tao [1 ,2 ]
Hsueh, Po-Ren [5 ]
Xu, Ying-Chun [1 ,2 ]
机构
[1] Chinese Acad Med Sci, Peking Union Med Coll Hosp, Dept Clin Lab, 1 Shuaifuyuan, Beijing 100730, Peoples R China
[2] Beijing Key Lab Mech Res & Precis Diag Invas Fung, Beijing, Peoples R China
[3] Chinese Acad Med Sci, Grad Sch, Peking Union Med Coll, Beijing, Peoples R China
[4] Chinese Acad Med Sci, Peking Union Med Coll Hosp, Med Res Ctr, Beijing, Peoples R China
[5] Natl Taiwan Univ, Coll Med, Dept Lab Med Internal Med, Natl Taiwan Univ Hosp, Taipei, Taiwan
关键词
Penicillium; Talaromyces; Internal transcribed spacer region; beta-Tubulin; RNA polymerase II second largest subunit gene; Antifungal susceptibility; FUNGAL ENDOPHTHALMITIS; EMERGING PATHOGEN; AMPHOTERICIN-B; MARNEFFEI; IDENTIFICATION; INFECTION; CHRYSOGENUM; PNEUMONIA; CITRINUM; ITRACONAZOLE;
D O I
10.1016/j.ijantimicag.2021.106349
中图分类号
R51 [传染病];
学科分类号
100401 ;
摘要
Morphologically identified Penicillium (n = 103) and Talaromyces marneffei (n = 8) isolates were collected from various clinical sources between 2016 and 2017 at a medical centre in Beijing, China. Identification to species level was confirmed by sequencing of the internal transcribed spacer (ITS) region, beta-tubulin gene (benA) and RNA polymerase II second largest subunit (RPB2) gene. Of the 111 isolates, 56 (50.5%) were identified as Penicillium spp. and 55 (49.5%) as Talaromyces spp. Eleven species of Penicillium were detected, of which Penicillium oxalicum was the commonest, accounting for 51.8% (29/56), followed by Penicillium rubens (10.7%; 6/56) and Penicillium citrinum (10.7%; 6/56). Among the 55 Talaromyces isolates, nine species were identified, with Talaromyces funiculosus (36.4%; 20/55), Talaromyces stollii (27.3%; 15/55) and Talaromyces marneffei (14.5%; 8/55) being the most common. Of note, 89.3% (50/56) of the Penicillium isolates and 98.2% (54/55) of the Talaromyces isolates exhibited growth at 37 degrees C. The isolates were mainly recovered from patients with pulmonary disorders (56.8%; 63/111), autoimmune disease (12.6%; 14/111) and AIDS (5.4%; 6/111). The azoles and amphotericin B exhibited potent activity against T. marneffei, while various levels of activity were observed against Penicillium and other Talaromyces species The echinocandins had the lowest MECs (MEC90, <= 0.12 mg/L) against most Penicillium and Talaromyces species, with the exception of T. marneffei whose MEC90 (4 mg/L) was five or more dilutions higher than that of the other species tested. These data on the species distribution and antifungal susceptibility expand the current clinical knowledge of Penicillium and Talaromyces species. (C) 2021 Published by Elsevier Ltd.
引用
收藏
页数:8
相关论文
共 41 条
[1]   Molecular epidemiology of otomycosis in Isfahan revealed a large diversity in causative agents [J].
Aboutalebian, Shima ;
Mahmoudi, Shahram ;
Mirhendi, Hossein ;
Okhovat, Ahmadreza ;
Abtahi, Hamidreza ;
Chabavizadeh, Javaher .
JOURNAL OF MEDICAL MICROBIOLOGY, 2019, 68 (06) :918-923
[2]  
Atalay Altay, 2016, Infez Med, V24, P153
[3]   Disseminated penicilliosis due to Penicillium chrysogenum in a pediatric patient with Henoch-Schonlein syndrome [J].
Aviles-Robles, Martha ;
Gomez-Ponce, Carlos ;
Resendiz-Sanchez, Jesus ;
Veronica Rodriguez-Tovar, Aida ;
Ceballos-Bocanegra, Adrian ;
Martinez-Rivera, Angeles .
INTERNATIONAL JOURNAL OF INFECTIOUS DISEASES, 2016, 51 :78-80
[4]   DNA and the classical way: Identification of medically important molds in the 21st century [J].
Balajee, S. Arunmozhi ;
Sigler, Lynne ;
Brandt, Mary E. .
MEDICAL MYCOLOGY, 2007, 45 (06) :475-490
[5]  
Barbara D., 2017, Reference Method for Broth Dilution Antifungal susceptibility testing of filamentous fungi
[6]   Intestinal invasion and disseminated disease associated with Penicillium chrysogenum [J].
Barcus A.L. ;
Burdette S.D. ;
Herchline T.E. .
Annals of Clinical Microbiology and Antimicrobials, 4 (1)
[7]   Talaromycosis (Penicilliosis) Due to Talaromyces (Penicillium) marneffei: Insights into the Clinical Trends of a Major Fungal Disease 60 Years After the Discovery of the Pathogen [J].
Cao, Cunwei ;
Xi, Liyan ;
Chaturvedi, Vishnu .
MYCOPATHOLOGIA, 2019, 184 (06) :709-720
[8]   In vitro interactions of micafungin with amphotericin B, itraconazole or fluconazole against the pathogenic phase of Penicillium marneffei [J].
Cao, Cunwei ;
Liu, Wei ;
Li, Ruoyu ;
Wan, Zhe ;
Qiao, Jianjun .
JOURNAL OF ANTIMICROBIAL CHEMOTHERAPY, 2009, 63 (02) :340-342
[9]   Talaromyces (Penicillium) marneffei infection in non-HIV-infected patients [J].
Chan, Jasper F. W. ;
Lau, Susanna K. P. ;
Yuen, Kwok-Yung ;
Woo, Patrick C. Y. .
EMERGING MICROBES & INFECTIONS, 2016, 5
[10]   Evaluation of the matrix-assisted laser desorption/ionization time-of-flight mass spectrometry Bruker Biotyper for identification of Penicillium marneffei, Paecilomyces species, Fusarium solani, Rhizopus species, and Pseudallescheria boydii [J].
Chen, Ying-Sheng ;
Liu, Yen-Hung ;
Teng, Shih-Hua ;
Liao, Chun-Hsing ;
Hung, Chien-Ching ;
Sheng, Wang-Huei ;
Teng, Lee-Jene ;
Hsueh, Po-Ren .
FRONTIERS IN MICROBIOLOGY, 2015, 6