Dematiaceous fungal keratitis: prevalence, spectrum, clinical features, outcome, and antifungal susceptibility from a tertiary care centre in North India.

IF 3.5 3区 医学 Q3 INFECTIOUS DISEASES
Ankita Saroya, Amit Gupta, Shivaprakash M Rudramurthy, Chintan Malhotra, Parul Chawla Gupta, Snigdha Reddy, Vrinda Sharma, Indu Dhiman, Harsimran Kaur, Anup K Ghosh
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Abstract

Fungal keratitis (FK) is a sight-threatening corneal infection that leads to corneal blindness. Dematiaceous fungal keratitis (DFK) emerged as the predominant cause of FK, followed by Aspergillus spp. and Fusarium spp. This study aimed the prevalence, species distribution, associated clinical features, risk factors, and antifungal susceptibility for keratitis caused by dematiaceous fungi. A prospective study was conducted on suspected FK patients from June 2023 through November 2025 at PGIMER Chandigarh. The corneal samples were processed for routine mycological investigations, including direct microscopy potassium hydroxide (KOH mount) and culture on SDA (Sabouraud's Dextrose agar), further confirmed by DNA sequencing. Antifungal susceptibility testing (AFST) was performed as per the CLSI (Clinical Laboratory and Standards Institute) broth microdilution method (M38-A2) for a panel of nine drugs, including voriconazole, itraconazole, posaconazole, luliconazole, miconazole, ketoconazole, amphotericin-B, natamycin, and terbinafine. Among 1931 suspected FK patients, 452 were confirmed FK where 75 were DFK and prevalence of DFK was calculated 3.88%. Curvularia spp. was found to be most prevalent (n = 39,52%), followed by Alternaria spp. (n = 9, 12%), Colletotrichum spp. (n = 8,10.66%), and Exserohilum spp. (n = 6, 8%) along with eight other rare genera were isolated. Redness, watering, and a decrease in vision were significantly more common in DFK. Amongst the triazoles, voriconazole showed low minimum inhibitory concentration (MIC) range of 0.03-16 µg/ml. AFST also demonstrated low MICs to luliconazole and terbinafine. The present study showed a prevalence of 3.88% DFK in North India with Curvularia spp. as the predominant causative agent. In vitro susceptibility of voriconazole demonstrated better performance against DFK isolates.

脱脂性真菌性角膜炎:患病率,频谱,临床特征,结果和抗真菌敏感性从印度北部的三级保健中心。
真菌性角膜炎是一种威胁视力的角膜感染,可导致角膜失明。摘要本研究旨在了解赤霉病真菌性角膜炎的流行、种类分布、相关临床特征、危险因素及抗真菌药敏性。从2023年6月到2025年11月,在昌迪加尔PGIMER医院对疑似真菌性角膜炎(FK)患者进行了一项前瞻性研究。对角膜样品进行常规真菌学研究,包括直接显微镜(KOH mount)和SDA (Sabouraud’s Dextrose agar)培养,并通过DNA测序进一步证实。采用CLSI (Clinical Laboratory and Standards Institute)肉汤微量稀释法(M38-A2)对伏立康唑、伊曲康唑、泊沙康唑、露立康唑、咪康唑、酮康唑、两性霉素- b、那他霉素、特比萘芬等9种药物进行抗真菌药敏试验。在1931例疑似FK患者中,确诊FK 452例,其中DFK 75例,DFK患病率计算为3.8%。其中以曲霉属(Curvularia spp.)最常见(n = 39,52%),其次为Alternaria spp.(n = 9, 12%)、Colletotrichum spp.(n = 8,10.66%)、exserhilum spp.(n = 6, 8%)等8个罕见属。红肿、流泪和视力下降在DFK患者中更为常见。三唑类药物中伏立康唑的MIC值较低,为0.03 ~ 16µg/ml。AFST也显示对鲁立康唑和特比萘芬的mic较低。本研究显示,印度北部DFK患病率为3.88%,主要病原体为曲孢菌。伏立康唑对DFK菌株的体外敏感性较好。
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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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