Deep Sequencing Reveals Mixed Infection with 2009 Pandemic Influenza A (H1N1) Virus Strains and the Emergence of Oseltamivir Resistance

被引:87
作者
Ghedin, Elodie [1 ,6 ]
Laplante, Jennifer [3 ]
DePasse, Jay [1 ]
Wentworth, David E. [3 ,4 ]
Santos, Roberto P. [5 ]
Lepow, Martha L. [5 ]
Porter, Joanne [5 ]
Stellrecht, Kathleen [5 ]
Lin, Xudong [3 ]
Operario, Darwin [3 ]
Griesemer, Sara [3 ]
Fitch, Adam [1 ]
Halpin, Rebecca A. [6 ]
Stockwell, Timothy B. [6 ]
Spiro, David J. [6 ]
Holmes, Edward C. [2 ,7 ]
St George, Kirsten [3 ]
机构
[1] Univ Pittsburgh, Sch Med, Ctr Vaccine Res, Dept Computat & Syst Biol, Pittsburgh, PA 15261 USA
[2] Penn State Univ, Dept Biol, Ctr Infect Dis Dynam, University Pk, PA 16802 USA
[3] SUNY Albany, Wadsworth Ctr, New York State Dept Hlth, Albany, NY 12222 USA
[4] SUNY Albany, Sch Publ Hlth, Dept Biomed Sci, Albany, NY 12222 USA
[5] Albany Med Ctr, Albany, NY USA
[6] J Craig Venter Inst, Rockville, MD USA
[7] NIH, Fogarty Int Ctr, Bethesda, MD 20892 USA
基金
美国国家卫生研究院;
关键词
MOLECULAR MARKERS; GENOME ANALYSIS; THERAPY;
D O I
10.1093/infdis/jiq040
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Mixed infections with seasonal influenza A virus strains are a common occurrence and an important source of genetic diversity. Prolonged viral shedding, as observed in immunocompromised individuals, can lead to mutational accumulation over extended periods. Recently, drug resistance was reported in immunosuppressed patients infected with the 2009 pandemic influenza A (H1N1) virus within a few days after oseltamivir treatment was initiated. To better understand the evolution and emergence of drug resistance in these circumstances, we used a deep sequencing approach to survey the viral population from an immunosuppressed patient infected with H1N1/2009 influenza and treated with neuraminidase inhibitors. This patient harbored 3 genetic variants from 2 phylogenetically distinct viral clades of pandemic H1N1/2009, strongly suggestive of mixed infection. Strikingly, one of these variants also developed drug resistance de novo in response to oseltamivir treatment. Immunocompromised individuals may, therefore, constitute an important source of genetic and phenotypic diversity, both through mixed infection and de novo mutation.
引用
收藏
页码:168 / 174
页数:7
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