کد مقاله کد نشریه سال انتشار مقاله انگلیسی نسخه تمام متن
5533393 1402121 2016 9 صفحه PDF دانلود رایگان
عنوان انگلیسی مقاله ISI
Mapping the Resistance Potential of Influenza's H+ Channel against an Antiviral Blocker
موضوعات مرتبط
علوم زیستی و بیوفناوری بیوشیمی، ژنتیک و زیست شناسی مولکولی بیولوژی سلول
پیش نمایش صفحه اول مقاله
Mapping the Resistance Potential of Influenza's H+ Channel against an Antiviral Blocker
چکیده انگلیسی


- Viruses are a serious threat due to their ability to constantly mutate and develop resistance to medical treatment.
- A genetic screen is developed to exhaustively map the resistance options of a virus against an antiviral drug.
- When applied to drugs that inhibit influenza by blocking its H+ channel, we were able to obtain known clinical resistance mutations.
- We provide an approach, which is ahead of any clinical use, to determine how influenza will develop resistance against antiviral drugs that block its H+ channel.

The development of drug resistance has long plagued our efforts to curtail viral infections in general and influenza in particular. The problem is particularly challenging since the exact mode of resistance may be difficult to predict, without waiting for untreatable strains to evolve. Herein, a different approach is taken. Using a novel genetic screen, we map the resistance options of influenza's M2 channel against its aminoadamantane antiviral inhibitors. In the process, we could identify clinically known resistant mutations in a completely unbiased manner. Additionally, novel mutations were obtained, which, while known to exist in circulating viruses, were not previously classified as drug resistant. Finally, we demonstrated the approach against an anti-influenza drug that has not seen clinical use, identifying several resistance mutations in the process. In conclusion, we present and employ a method to predict the resistance options of influenza's M2 channel to antiviral agents ahead of clinical use and without medical hazard.

Graphical Abstract219

ناشر
Database: Elsevier - ScienceDirect (ساینس دایرکت)
Journal: Journal of Molecular Biology - Volume 428, Issue 20, 9 October 2016, Pages 4209-4217
نویسندگان
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