Aspergillosis coinfection in patients with proven mucormycosis.

IF 2.7 3区 医学 Q3 INFECTIOUS DISEASES Medical mycology Pub Date : 2024-08-02 DOI:10.1093/mmy/myae081
Sang Hyun Ra, Ji Yeun Kim, Joon Seon Song, Hyeon Mu Jang, Euijin Chang, Seongman Bae, Jiwon Jung, Min Jae Kim, Yong Pil Chong, Sang-Oh Lee, Sang-Ho Choi, Yang Soo Kim, Sung-Han Kim
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Abstract

Although research on aspergillosis and mucormycosis confection is important to optimize antifungal therapy, data on this issue is scarce. Thus, we systematically investigated aspergillosis coinfection in patients with proven mucormycosis. Medical records of adult patients with proven mucormycosis whose formalin-fixed paraffin-embedded (FFPE) tissue sections were available, in a tertiary hospital from August 2007 to July 2023 were retrospectively reviewed to assess coinfection with aspergillosis. We noted cultures of fungi from sterile and non-sterile sites and performed polymerase chain reaction (PCR) assays on FFPE tissues to detect Aspergillus- and Mucorales-specific DNA. Sixty-seven patients with proven mucormycosis, including 12 (18%) with a positive culture of the mucormycosis agent from sterile site cultures, were enrolled. Fungal cultures from sterile and non-sterile sites revealed Aspergillus spp. growth in nine (13%) of the 67 patients, including two sterile and seven non-sterile cultures. The fungal PCR analysis from the FFPE sections was positive for Aspergillus-specific PCR in five (7%) and positive for both Aspergillus- and Mucorales-specific PCR results in eight (12%). Overall, 21 (31%) of the 67 patients with proven mucormycosis had microbiologic and/or molecular evidence of aspergillosis coinfection. Positive blood or bronchoalveolar lavage fluid galactomannan results were more common in the coinfection group (67% [14/21]) than in the mucormycosis group (37% [17/46], P = .024). No significant difference in mortality between the two groups was observed. Approximately one-third of patients with proven mucormycosis exhibited molecular and/or microbiologic evidence of aspergillosis coinfection. Further research is needed to identify patients with aspergillosis and mucormycosis coinfections, for optimal antifungal therapy.

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已证实患有粘孢子菌病的患者合并曲霉菌病。
尽管对曲霉菌病和粘孢子菌病合并感染的研究对于优化抗真菌治疗非常重要,但这方面的数据却很少。因此,我们对已证实患有粘孢子菌病的患者的曲霉菌病合并感染情况进行了系统研究。我们回顾性审查了一家三甲医院自 2007 年 8 月至 2023 年 7 月期间证实患有粘孢子菌病的成年患者的病历,这些患者均有福尔马林固定石蜡包埋(FFPE)组织切片,我们评估了患者合并曲霉菌病的情况。我们注意到了无菌和非无菌部位的真菌培养物,并对 FFPE 组织进行了 PCR 检测,以检测曲霉菌和粘菌的特异性 DNA。67 名已证实患有粘孢子菌病的患者参加了此次研究,其中包括 12 名(18%)从无菌部位培养出的粘孢子菌病原体呈阳性的患者。从无菌和非无菌部位进行的真菌培养显示,67 名患者中有 9 人(13%)体内有曲霉菌生长,其中包括 2 例无菌培养和 7 例非无菌培养。对 FFPE 切片进行的真菌 PCR 分析显示,5 例(7%)患者的曲霉菌特异性 PCR 结果呈阳性,8 例(12%)患者的曲霉菌和粘菌特异性 PCR 结果均呈阳性。总体而言,在 67 名已证实患有粘孢子菌病的患者中,有 21 人(31%)有曲霉菌病合并感染的微生物学和/或分子证据。血液或支气管肺泡灌洗液半乳甘露聚糖阳性结果在合并感染组(67% [14/21])比在粘孢子菌病组(37% [17/46],P = 0.024)更常见。两组患者的死亡率无明显差异。在已证实患有粘孢子菌病的患者中,约有三分之一表现出曲霉菌病合并感染的分子和/或微生物学证据。需要进一步研究确定曲霉菌病和粘孢子菌病合并感染的患者,以便进行最佳抗真菌治疗。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Medical mycology
Medical mycology 医学-兽医学
CiteScore
5.70
自引率
3.40%
发文量
632
审稿时长
12 months
期刊介绍: Medical Mycology is a peer-reviewed international journal that focuses on original and innovative basic and applied studies, as well as learned reviews on all aspects of medical, veterinary and environmental mycology as related to disease. The objective is to present the highest quality scientific reports from throughout the world on divergent topics. These topics include the phylogeny of fungal pathogens, epidemiology and public health mycology themes, new approaches in the diagnosis and treatment of mycoses including clinical trials and guidelines, pharmacology and antifungal susceptibilities, changes in taxonomy, description of new or unusual fungi associated with human or animal disease, immunology of fungal infections, vaccinology for prevention of fungal infections, pathogenesis and virulence, and the molecular biology of pathogenic fungi in vitro and in vivo, including genomics, transcriptomics, metabolomics, and proteomics. Case reports are no longer accepted. In addition, studies of natural products showing inhibitory activity against pathogenic fungi are not accepted without chemical characterization and identification of the compounds responsible for the inhibitory activity.
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