Oseltamivir-resistant influenza A pandemic (H1N1) 2009 virus, Hong Kong, China.
Experimental evidence from animal models showed that this virus was able to replicate to high titers in the lungs of infected animals (4), unlike seasonal influenza viruses, which mainly infect the upper respiratory tract. Serologic studies found that antibodies induced by current seasonal influenza vaccines show little cross-reactivity to pandemic (H1N1) 2009 virus (5).
Therapeutic options are presently limited to 2 neuraminidase (NA) inhibitors, oseltamivir and zanamivir, because this virus has a swine-origin matrix 2 (M2) gene, which contains a mutation associated with resistance to M2 ion channel blockers amantadine and rimantadine. Although oseltamivir has been widely used in persons infected with pandemic (H1N1) 2009 virus, resistance was not observed until recently. Three unrelated cases of resistance to oseltamivir were observed in Denmark, Japan, and Hong Kong (www.who.int/csr/disease/swineflu/notes/ h1n1_antiviral_resistance_20090708/en/index.html).
Emergence of resistance to oseltamivir by seasonal influenza A virus (H1N1) was detected in Norway in 2007. This virus has evolved into the dominant influenza A virus (H1N1) in humans (6). This finding raises strong concerns that the 274Y resistant mutation in pandemic (H1N1) 2009 virus might circulate and become dominant. We report virologic investigation of the emergence of oseltamivir resistance in this virus in a patient from Hong Kong.
A 16-year-old previously healthy girl had a fever at the Hong Kong International Airport after her arrival from San Francisco, California, USA, on June 11, 2009. Physical examination showed a temperature of 38.3[degrees]C, a blood pressure of 117/66 mm Hg, a pulse rate of 94 beats/min, and an oxygen saturation of 99% at room air. Results of a complete blood count and liver and renal function tests were normal. She had a leukocyte count of 4.69 x [10.sup.9] cells/L, an absolute neutrophil count of 2.36 x [10.sup.9] cells/L, and a lymphocyte count of 1.74 x [10.sup.9] cells/L. Findings on her chest radiograph were normal.
A nasopharyngeal aspirate (NPA) was positive for influenza A virus (H1N1) nucleoprotein by immunofluorescence. NPA specimens on days 1 and 5 were positive for influenza A virus (H1N1) M gene and swine-specific specific H1 gene by reverse transcription-PCR (RT-PCR). Samples obtained on days 6-8 were negative. Serum and midstream urine specimens obtained on day 2 were negative for influenza A virus (H1N1) M gene by RT-PCR.
The patient refused antiviral therapy with oseltamivir because of fear of its potential side effects. She was then offered symptomatic treatment. Her clinical condition gradually improved and she was discharged on day 8 uneventfully.
Influenza A pandemic (H1N1) 2009 virus was cultured from NPA. Subsequent drug susceptibility testing showed that this isolate was resistant to oseltamivir (50% inhibitory concentration 197.5 nM), but susceptible to zanamivir, as determined by enzymatic assay (Table).
To confirm whether the virus contained mutations associated with resistance to NA inhibitors, NA sequences from the day 1 NPA specimen and an MDCK cell isolate were examined. Viral RNA was extracted from NPA and MDCK cell supernatants by using reported procedures (7). RT-PCR was performed by using primers spanning position 274 of the NA gene (forward: 5'-ACACAAGAGTCTGAATGTGCATGT-3'; reverse: 5'-GTCTCCGAAAATCCCACTGCATAT-3'). Direct sequencing of PCR products was performed by using a BigDye Terminator v3.1 cycle sequencing reaction kit on an ABI PRISM 3730 DNA analyzer (Applied Biosystems, Foster City, CA, USA).
Sequences indicated that the NA genes in the NPA and MDCK cell virus isolates contained an H [right arrow] Y mutation at the NA 274 (H3 numbering, 275 in H1 numbering) residue (GenBank accession no. GQ351316). No other NA mutations known to be associated with oseltamivir resistance were observed. Further examination of sequences showed mixed populations (T/C) in the NA gene from the NPA specimen (Figure, panel A).
Estimation of 274H and 274Y populations in the NPA specimen was performed by cloning and sequencing PCR products. The NPA specimen contained approximately equal proportions of 274Y and 274H (52.63% and 47.37%, respectively). Examination of sequences from the MDCK cell isolate showed predominantly the 274Y type, although a minor 274H peak was also observed (Figure, panel B). Cloning and sequencing of PCR products from the MDCK virus isolate showed that 97.92% of the NA genes were 274Y, which suggests that the 274Y population overtook the 274H population during MDCK cell culture.
Resistance to NA inhibitors among seasonal strains of human influenza viruses (A/H1N1, A/H3N2, and B) has been rare until recently. Development of resistance after oseltamivir treatment has occurred in 0.33%-5.5% of treated patients (8). Oseltamivir resistance associated with the NA 274Y genotype was also observed in human infections with avian influenza A virus (H5N1) (9,10). Low levels of 274Y quasi-species in avian influenza A viruses (H5N1) from avian hosts has been reported (11). Oseltamivir-resistant human influenza A viruses (H3N2 and H1N1) have been found to replicate less efficiently than oseltamivir-susceptible strains in cell culture and animal models (12-14). However, the NA 274Y resistant mutant in highly pathogenic avian influenza A virus (H5N1) retained the high pathogenicity of wild-type virus in mammalian species (15).
In 2007, an NA H274Y oseltamivir-resistant variant of seasonal influenza A virus (H1N1) was detected in Norway (6). This virus has now become the dominant virus population globally, overtaking oseltamivir-susceptible influenza A virus (H1N1). The molecular basis for the 274Y variant in seasonal influenza A virus (H1N1) virus and the mechanism by which this resistant variant became the dominant population remain unknown.
Lack of general immunity to pandemic (H1N1) 2009 virus in the human population, combined with the inherent adamantane resistance of the virus, indicates that NA inhibitors constitute the primary treatment regimen for susceptible patient groups and those in whom severe diseases develop during the current pandemic. There is great concern that an oseltamivir-resistant variant of pandemic (H1N1) 2009 virus may emerge and circulate in a manner similar to oseltamivir-resistant seasonal influenza A virus (H1N1).
The patient in this study was not treated with oseltamivir. Therefore it is unlikely that the 274Y mutation was drug-induced. Detection of mixed populations of 274Y and 274H in the NPA specimen before antiviral treatment suggests that the mutation occurs naturally, either before or during infection. Although no experimental data exist that show the growth properties of this resistant variant, examination of the quasi-species population in the cell culture-propagated virus isolate showed that the 274Y variant has become the dominant population. This finding implies that the 274Y mutation does not compromise replication of pandemic (H1N1) 2009 virus in vitro.
Quarantine procedures adopted by the Hong Kong Special Administrative Region in China during the early containment phase might have limited transmission of this variant virus. Knowledge of this virus is still limited, and characterization of transmission properties of this resistant variant in in vitro and in vivo models is needed. Moreover, pandemic (H1N1) 2009 virus should be closely monitored for emergence of resistant variants.
We thank W. Lim and her staff for support. This study was partly supported by the Providence Foundation Limited in memory of the late Lui Hac Minh, the Research Grants Council of the Hong Kong Special Administrative Region (7500/06M), the Research Fund for the Control of Infectious Diseases of the Food and Health Bureau of the Hong Kong Government, University Development Fund 2001-2002 (first round) of The University of Hong Kong, and the Clinical Infectious Diseases Research Endowment Fund.
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Honglin Chen, Chung Lam Cheung, Hung Tai, Pengxi Zhao, Jasper F.W. Chan, Vincent C.C. Cheng, Kwok-Hung Chan, and Kwok-Yung Yuen
Author affiliation: The University of Hong Kong, Hong Kong Special Administrative Region, People's Republic of China
Address for correspondence: Kwok-Yung Yuen, Department of Microbiology, Centre for Infection and Division of Infectious Diseases, The University of Hong Kong, Queen Mary Hospital, Pokfulam Rd, Pokfulam, Hong Kong Special Administrative Region, People's Republic of China; email: email@example.com
Dr Chen is an associate professor at The University of Hong Kong. His primary research interests are molecular basis of antigenic variation and host-restricting factors of influenza virus.
Table. Quasi/species of 274H and 274 Y pandemic (H1N1) 2009 virus from NPA samples and subsequent virus isolate A/Hong Kong/2369/2009 from MDCK cells conferring resistance to oseltamivir, Hong Kong, China * 274H, no. samples 274Y, no. samples Sample positive/no. tested (%) positive/no. tested (%) NPA 45/95 (47.37) 50/95 (52.63) MDCK cell culture 2/96 (2.08) 94/96 (97.92) [IC.sub.50] for [IC.sub.50] for Sample oseltamivir, nM zanamivir, nM NPA ND ND MDCK cell culture 197.5 0.8 * 50% inhibitory concentrations ([IC.sub.50s]) for oseltamivir and zanamivir were determined by using NA-Star influenza neuraminidase (NA) inhibitor resistance detection kits (Applied Biosystems, Foster City, CA, USA) according to the manufacturer's instructions. Ratios of 274H and 274Y were evaluated by cloning neuraminidase (NA) gene PCR products from nasopharyngeal aspirate (NPA) samples or MDCK cell-cultured virus into the TA vector (Invitrogen, Carlsbad, CA, USA) and sequencing clones containing the NA gene. ND, not done.
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|Author:||Chen, Honglin; Cheung, Chung Lam; Tai, Hung; Zhao, Pengxi; Chan, Jasper F.W.; Cheng, Vincent C.C.; C|
|Publication:||Emerging Infectious Diseases|
|Date:||Dec 1, 2009|
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