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4.
Rev Med Virol ; 32(4): e2310, 2022 07.
Artículo en Inglés | MEDLINE | ID: covidwho-1490910

RESUMEN

Severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) is a novel human coronavirus and the causative agent of coronavirus disease 2019 (Covid-19). There is an urgent need for effective antivirals to treat current Covid-19 cases and protect those unable to be vaccinated against SARS-CoV-2. Marine molluscs live in an environment containing high virus densities (>107 virus particles per ml), and there are an estimated 100,000 species in the phylum Mollusca, demonstrating the success of their innate immune system. Mollusc-derived antivirals are yet to be used clinically despite the activity of many extracts, including against human viruses, being demonstrated in vitro. Hemolymph of the Pacific oyster (Crassostrea gigas) has in vitro antiviral activity against herpes simplex virus and human adenovirus, while antiviral action against SARS-CoV-2 has been proposed by in silico studies. Such evidence suggests that molluscs, and in particular C. gigas hemolymph, may represent a source of antivirals for human coronaviruses.


Asunto(s)
Tratamiento Farmacológico de COVID-19 , SARS-CoV-2 , Animales , Antivirales/farmacología , Antivirales/uso terapéutico , Humanos
5.
Future Microbiol ; 16(3): 135-142, 2021 02.
Artículo en Inglés | MEDLINE | ID: covidwho-1110198

RESUMEN

The ability of influenza A virus to evolve, coupled with increasing antimicrobial resistance, could trigger an influenza pandemic with great morbidity and mortality. Much of the 1918 influenza pandemic mortality was likely due to bacterial coinfection, including Staphylococcus aureus pneumonia. S. aureus resists many antibiotics. The lack of new antibiotics suggests alternative antimicrobials, such as bacteriophages, are needed. Potential delivery routes for bacteriophage therapy (BT) include inhalation and intravenous injection. BT has recently been used successfully in compassionate access pulmonary infection cases. Phage lysins, enzymes that hydrolyze bacterial cell walls and which are bactericidal, are efficacious in animal pneumonia models. Clinical trials will be needed to determine whether BT can ameliorate disease in influenza and S. aureus coinfection.


Asunto(s)
Bacteriófagos/fisiología , Coinfección/terapia , Virus de la Influenza A/fisiología , Gripe Humana/terapia , Terapia de Fagos , Neumonía Estafilocócica/terapia , Staphylococcus aureus/virología , Animales , Coinfección/microbiología , Coinfección/mortalidad , Coinfección/virología , Humanos , Virus de la Influenza A/genética , Gripe Humana/mortalidad , Gripe Humana/virología , Neumonía Estafilocócica/microbiología , Neumonía Estafilocócica/mortalidad , Staphylococcus aureus/genética , Staphylococcus aureus/fisiología
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