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A qPCR identification scheme to detect the most common causative agents of actinomycetoma in Africa

A qPCR identification scheme to detect the most common causative agents of actinomycetoma in Africa
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Researchers have developed a new multiplex qPCR identification scheme to rapidly detect the causative agents of actinomycetoma in Africa. This method significantly reduces the time required for diagnosis compared to traditional histology and culturing techniques.

Why it matters

Faster diagnosis of this neglected tropical disease allows for earlier treatment, potentially preventing severe physical mutilation.

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Mycetoma is a neglected tropical disease characterized by mutilating tumorous lesions in the subcutaneous tissue. The causative agents are found embedded in granules called grains. Mycetoma is either caused by bacteria (actinomycetoma) or fungi (eumycetoma). To initiate the appropriate treatment, it is important to identify the causative agent rapidly and molecular identification for eumycetoma revolutionized the time to identification. For actinomycetoma this was not possible yet. Here we developed a multiplex qPCR identification scheme for the most common causative agents of actinomycetoma in Africa. Whole genome sequencing was used to identify species-specific gene families for Actinomadura madurae, Actinomadura pelletieri, Streptomyces somaliensis and Streptomyces sudanensis . qPCR primers and probes were developed on these species and validated against DNA isolated from mycetoma strains and grains. Each probe was unique with no cross-reactivity with other tested species. The limit of detection ranged from 0.000013 to 0.00067 ng bacterial DNA.

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