scholarly journals Surveillance for Oseltamivir-Resistant Influenza A(H1N1)pdm09 Virus Infections During 2015–2016, United States

2016 ◽  
Vol 3 (suppl_1) ◽  
Author(s):  
Sarah Spencer ◽  
Ha Nguyen ◽  
Anwar Abd Elal ◽  
Angela P. Campbell ◽  
Jennifer Laplante ◽  
...  
2012 ◽  
Vol 82 (3) ◽  
pp. 187-193 ◽  
Author(s):  
M. Jonges ◽  
J. Rahamat-Langendoen ◽  
A. Meijer ◽  
H.G. Niesters ◽  
M. Koopmans

2013 ◽  
Vol 13 (1) ◽  
Author(s):  
John J McKenna ◽  
◽  
Anna M Bramley ◽  
Jacek Skarbinski ◽  
Alicia M Fry ◽  
...  

2019 ◽  
Vol 8 (1) ◽  
pp. 404-412 ◽  
Author(s):  
Herath M. T. K. Karunarathna ◽  
Ranawaka A. P. M. Perera ◽  
Vicky J. Fang ◽  
Hui-ling Yen ◽  
Benjamin John Cowling ◽  
...  

2012 ◽  
Vol 18 (9) ◽  
pp. 1519-1521 ◽  
Author(s):  
Gregory C. Gray ◽  
Jeffrey B. Bender ◽  
Carolyn B. Bridges ◽  
Russell F. Daly ◽  
Whitney S. Krueger ◽  
...  

2018 ◽  
Vol 5 (suppl_1) ◽  
pp. S267-S268 ◽  
Author(s):  
Sarah Spencer ◽  
Ha Nguyen ◽  
Anwar Abd Elal ◽  
Jennifer Laplante ◽  
Kirsten St George ◽  
...  

Abstract Background Three neuraminidase inhibitors (NAIs) are approved and recommended for treatment of influenza in the United States; however, antiviral resistance can emerge during or after treatment, and sporadic resistant viruses unrelated to NAI exposure may occur, especially in influenza A(H1N1)pdm09 viruses. Limited transmission of oseltamivir-resistant A(H1N1)pdm09 viruses between persons has also occurred. Oseltamivir resistance is most commonly caused by an H275Y substitution in the neuraminidase (NA). We describe findings from surveillance for oseltamivir-resistant A(H1N1)pdm09 viruses. Methods The CDC requested state public health laboratories to submit up to eight viruses (two of each subtype/lineage) every 2 weeks for virus sequencing and NA inhibition assay testing; up to five additional A(H1N1)pdm09 clinical specimens were requested for H275Y pyrosequencing. NA sequencing and functional phenotypic NA inhibition assays were performed on drug-resistant virus isolates. A standard case form was collected on persons infected with oseltamivir-resistant viruses. Results From October 1, 16 to April 18, 18, 1,368 A(H1N1)pdm09 viruses were tested (median 89 specimens, range 20–328, tested/month during the influenza season). Overall, 12 (~0.9%) oseltamivir-resistant A(H1N1)pdm09 viruses were detected from nine states; all contained H275Y in the NA. All viruses were also resistant to peramivir, but none to zanamivir. The 12 patients had a median age of 34 years (range, 2 months–69 years). Eight (67%) had an immunosuppressive condition. Six (50%) reported no exposure to NAIs before specimen collection, two were taking oseltamivir (for 1 and 20 days) at the time of specimen collection, and antiviral receipt was unknown for 4. Three (23%) patients were hospitalized; there were no deaths. Conclusion During the 2016–2017 and 2017–2018 influenza seasons, influenza A(H1N1)pdm09 viruses resistant to both oseltamivir and peramivir were infrequently detected; all retained susceptibility to zanamivir. Among those with available information, half had no exposure to oseltamivir. Viruses harboring H275Y continue to circulate at low levels in the community. Ongoing surveillance for trends in oseltamivir- and peramivir-resistant A(H1N1)pdm09 is critical to inform clinical care and public health policies. Disclosures All authors: No reported disclosures.


2013 ◽  
Vol 19 (3) ◽  
Author(s):  
Rebekah H. Borse ◽  
Sundar S. Shrestha ◽  
Anthony E. Fiore ◽  
Charisma Y. Atkins ◽  
James A. Singleton ◽  
...  

2011 ◽  
Vol 173 (10) ◽  
pp. 1121-1130 ◽  
Author(s):  
D. L. Chao ◽  
L. Matrajt ◽  
N. E. Basta ◽  
J. D. Sugimoto ◽  
B. Dean ◽  
...  

Author(s):  
Diqi Yang ◽  
Minghua Hu ◽  
Hongmei Zhu ◽  
Jianguo Chen ◽  
Dehai Wang ◽  
...  

Abstract The pandemic influenza A (H1N1) virus spread globally and posed one of the most serious global public health challenges. The traditional Chinese medicine is served as a complementary treatment strategy with vaccine immunization. Here, we demonstrated the mixed polysaccharides (MPs) derived from shiitake mushroom, poriacocos, ginger and tyangerine peel prevent the H1N1 virus infections in mice. MPs pretreatment attenuated H1N1 virus-induced weight loss, clinical symptoms and death. The lymphocytes detection results showed the CD3+, CD19+ and CD25+ cell proportions were up-regulated in thymus under MPs pretreatment. Besides, MPs pretreatment reduced the inflammatory cell infiltration and increased the cell proportions of CD19+, CD25+ and CD278+ in lung. However, MPs treatment have no effective therapeutic effect after H1N1 virus challenge. The current study suggested that pretreatment with MPs could attenuate H1N1 virus-induced lung injury and up-regulate humoral and cellular immune responses in non- immunized mice.


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