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Paediatr Respir Rev ; 46: 63-70, 2023 Jun.
Artículo en Inglés | MEDLINE | ID: mdl-36828670

RESUMEN

Nontuberculous mycobacteria (NTM) can cause severe pulmonary disease in people with cystic fibrosis (pwCF). These infections present unique challenges for diagnosis and treatment, prompting a recent interest in understanding NTM transmission and pathogenesis during chronic infection. Major gaps remain in our knowledge regarding basic pathogenesis, immune evasion strategies, population dynamics, recombination potential, and the evolutionary implications of host and antibiotic pressures of long-term NTM infections in pwCF. Phylogenomic techniques have emerged as an important tool for tracking global patterns of transmission and are beginning to be used to ask fundamental biological questions about adaptation to the host during pathogenesis. In this review, we discuss the burden of NTM lung disease (NTM-LD), highlight the use of phylogenomics in NTM research, and address the clinical implications associated with these studies.


Asunto(s)
Fibrosis Quística , Infecciones por Mycobacterium no Tuberculosas , Infecciones del Sistema Respiratorio , Humanos , Fibrosis Quística/complicaciones , Fibrosis Quística/microbiología , Filogenia , Infecciones por Mycobacterium no Tuberculosas/epidemiología , Micobacterias no Tuberculosas/genética , Infecciones del Sistema Respiratorio/complicaciones
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