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DOI 10.3389/fcimb.2021.774340

Медицинская библиотека · Frontiers in cellular and infection microbiology · 2021

Pathogen-Host Interaction Repertoire at Proteome and Posttranslational Modification Levels During Fungal Infections.

Li Yanjian, Li Hailong, Sun Tianshu, Ding Chen

СтатьяПоддержка исследования: вне правительства СШАОбзорПеревод пока не подготовлен

Аннотация

Prevalence of fungal diseases has increased globally in recent years, which often associated with increased immunocompromised patients, aging populations, and the novel Coronavirus pandemic. Furthermore, due to the limitation of available antifungal agents mortality and morbidity rates of invasion fungal disease remain stubbornly high, and the emergence of multidrug-resistant fungi exacerbates the problem. Fungal pathogenicity and interactions between fungi and host have been the focus of many studies, as a result, lots of pathogenic mechanisms and fungal virulence factors have been identified. Mass spectrometry (MS)-based proteomics is a novel approach to better understand fungal pathogenicities and host-pathogen interactions at protein and protein posttranslational modification (PTM) levels. The approach has successfully elucidated interactions between pathogens and hosts by examining, for example, samples of fungal cells under different conditions, body fluids from infected patients, and exosomes. Many studies conclude that protein and PTM levels in both pathogens and hosts play important roles in progression of fungal diseases. This review summarizes mass spectrometry studies of protein and PTM levels from perspectives of both pathogens and hosts and provides an integrative conceptual outlook on fungal pathogenesis, antifungal agents development, and host-pathogen interactions.

Для цитирования: Li Yanjian, Li Hailong, Sun Tianshu, Ding Chen. Pathogen-Host Interaction Repertoire at Proteome and Posttranslational Modification Levels During Fungal Infections.. Frontiers in cellular and infection microbiology. 2021. DOI: 10.3389/fcimb.2021.774340.

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