Abstract

Fusarium species have emerged as one of the more outstanding groups of clinically important filamentous fungi, causing localized and life-threatening invasive infections with high morbidity and mortality. The ability to produce different types of hydrolytic enzymes is thought to be an important virulence mechanism of fungal pathogens and could be associated with the environment of the microorganism. Here, we have measured the production of two distinct lipolytic enzymes, phospholipase and esterase, by sixteen Fusarium isolates recovered from the hospital environment, immunocompromised patients' blood cultures, foot interdigital space scrapings from immunocompromised patients, and foot interdigital space scrapings from immunocompetent patients (4 isolates each). Fourteen of these 16 isolates were identified as Fusarium solani species complex (FSSC) and two were identified as F. oxysporum species complex (FOSC). Some relevant genus characteristics were visualized by light and electron microscopy such as curved and multicelled macroconidia with 3 or 4 septa, microconidia, phialides, and abundant chlamydospores. All Fusarium isolates were able to produce esterase and phospholipase under the experimental conditions. However, a negative correlation was observed between these two enzymes, indicating that a Fusarium isolate with high phospholipase activity has low esterase activity and vice versa. In addition, Fusarium isolated from clinical material produced more phospholipases, while environmental strains produced more esterases. These observations may be correlated with the different types of substrates that these fungi need to degrade during their nutrition processes.

Highlights

  • Fusarium species are important pathogens causing invasive fungal disease in severely immunocompromised patients, especially those with hematologic malignancies [1]

  • The aim of the present study was to determine the production of extracellular enzymes, such as phospholipase and esterase, by Fusarium species isolates recovered from biological material from immunocompetent and immunocompromised patients, and from the hospital environment

  • Fourteen of these 16 isolates were identified as F. solani species complex (FSSC) and two were identified as F. oxysporum species complex (FOSC) by sequencing as previously described [2] and reported elsewhere [7]

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Summary

Introduction

Fusarium species are important pathogens causing invasive fungal disease in severely immunocompromised patients, especially those with hematologic malignancies [1]. The more frequent species causing human disease are Fusarium solani, F. oxysporum and F. moniliforme [1]. The identification of Fusarium species has been performed by observation of the macro- and micromorphologic characteristics of the mycelium and reproductive structures such as colony pigmentation, banana-shaped or oval conidial morphology, and the presence of multicellular macroconidia with a foot cell at the base. These methods are laborious, time-consuming and require a qualified professional. Molecular techniques have replaced morphological ones and are considered to be gold standard procedures for fungal identification [2]

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