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DOI 10.1016/j.diagmicrobio.2019.05.018

Медицинская библиотека · Diagnostic microbiology and infectious disease · 2019

Mixed secondary bacterial infection is associated with severe lesions of chromoblastomycosis in a neglected population from Brazil.

Marques Sirlei G, Bomfim Maria Rosa Q, Azevedo Conceição de Maria P S, Martins Cleide Viviane B, Marques Ana Claudia G, Gonçalves Azizedite G, Vicente Vania A, Dos Santos Alcione M, Costa Marliete C, Freitas Gustavo J C, Santos Daniel A, de Resende-Stoianoff Maria A

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Аннотация

Chromoblastomycosis (CBM) is a chronic subcutaneous infection caused by melanotic fungi, affecting mainly rural workers in tropical and subtropical regions. Secondary bacterial infections (SBIs) in CBM lesions bring complications to the disease, but little is known about the agents involved. Fungal and bacterial identification and epidemiological profile of 50 patients with CBM were analyzed in this study. Bacteria were tested for susceptibility to antibacterial drugs. Fonseacea pedrosoi and Rhinocladiella aquaspersa were the fungal agents isolated. 88% of the patients presented SBI. Gram-positive bacteria coinfected mainly upper limbs, and Gram-negative bacteria were more isolated from lower limbs. Streptococcus pyogenes and mixed bacterial microbiota were associated with severe lesions. Staphylococcus aureus was associated with mixed infections and consequently with the severity of the infection. Resistance to β-lactams and methicillin was detected. Our results emphasize the necessity of bacterial culture and susceptibility testing as part of routine monitoring CBM cases.

Для цитирования: Marques Sirlei G, Bomfim Maria Rosa Q, Azevedo Conceição de Maria P S, Martins Cleide Viviane B, Marques Ana Claudia G, Gonçalves Azizedite G, Vicente Vania A, Dos Santos Alcione M, Costa Marliete C, Freitas Gustavo J C, Santos Daniel A, de Resende-Stoianoff Maria A. Mixed secondary bacterial infection is associated with severe lesions of chromoblastomycosis in a neglected population from Brazil.. Diagnostic microbiology and infectious disease. 2019. DOI: 10.1016/j.diagmicrobio.2019.05.018.

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