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Mycetoma

Mycetoma encompasses a diverse range of cutaneous and subcutaneous infections that present notable complexities, arising from either fungi (eumycetomas) or bacteria (actinomycetomas). Setting a distinguished mark in the realm of infectious diseases such as mycetoma, our company excels by providing specialized, all-inclusive services designed for researchers and scientists in this unique domain.

Overview of Mycetoma

Mycetoma is a chronic granulomatous inflammatory disease that affects the skin, subcutaneous tissue, and sometimes even bones. Prevalent in regions identified as the "mycetoma belt" like Africa, South America, and South Asia, this disease is characterized by distinct features such as the formation of localized swellings and sinus tracts that release grains comprising fungal or bacterial components.

The prevalence distribution of mycetoma.Fig.1 Prevalence of mycetoma. (Develoux M., 2022)

Pathogenesis of Mycetoma

Mycetoma pathogens typically enter the body through breaks in the skin, such as wounds or injuries, locally incubate and proliferate, and then progress to visible lesions. Should the infection remain untreated, the pathogens have the potential to advance through muscular fascial spaces and lymphatics, extending their reach to muscles and bones. The consequences of such progression can be severe, leading to disfigurement, deformity, disability, limb amputation, and even death.

Staining results of mycetoma.Fig.2 Histopathology of eumycetoma. (Hao, X., et al., 2022)

Vaccine Development for Mycetoma

Developing a vaccine for mycetoma is challenging due to the complex nature of the disease, the diversity of causative agents, and the chronicity of the infection. There is ongoing research into potential vaccine candidates for mycetoma, but no widely accepted vaccine is currently available.

  • Peptide Vaccine
    Predicted by bioinformatics that the peptide FFKEHGVPL is likely to be the first proposed epitope-based vaccine against fructose-bisphosphate aldolase of Madurella mycetomatis.
  • Nocardia brasiliensis protease
    The caseinolytic protease from a Nocardia brasiliensis cell extract induced IgM and IgG anti-protease antibodies and prevented mycetoma development in infected animals.

Therapeutics Development for Mycetoma

Causative agents Drug Names Mechanism of Action Targets Research Phase
Eumycetoma Itraconazole Inhibit cell growth and promote cell death of fungi CYP51A1 Approved
Terbinafine Inhibit fungal ergosterol synthesis SQLE Approved
Ravuconazole Disrupt synthesis of ergosterol in the fungal cell membrane CYP51A1 Phase II trials
Fosravuconazole Inhibit cytochrome P450-dependent lanosterol 14α-demethylase CYP51A1 Clinical research
Actinomycetoma TMP-SMX Inhibits the enzyme systems related to bacterial tetrahydrofolic acid synthesis DHPS Approved
DA−7867 Active against a wide spectrum of actinobacteria / Preclinical research

Our Services

Our company stands at the forefront of infectious disease research, offering a unique advantage through advanced infectious disease models, vaccine development, and therapeutic development platforms. By supporting researchers with integrated solutions and cutting-edge tools, we are committed to driving progress in the fight against infectious diseases like mycetoma.

Featured Services of Mycetoma

Through our integrated methodology, we furnish researchers with a smooth pathway, spanning from experimental design to data analysis, allowing them to concentrate on progressing their endeavors and enriching the comprehension and therapy of infectious diseases such as mycetoma. If you are interested in our service, please don't hesitate to contact us.

References

  1. Develoux, Michel. "Epidemiologic Aspects of Mycetoma in Africa." Journal of fungi (Basel, Switzerland) 8.12 (2022): 1258.
  2. Hao, Xingpei et al. "Mycetoma: Development of Diagnosis and Treatment." Journal of fungi (Basel, Switzerland) 8.7 (2022): 743.

All of our services and products are intended for preclinical research use only and cannot be used to diagnose, treat or manage patients.