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Viral load in patients infected with pandemic H1N1 2009 influenza A virus

✍ Scribed by Kelvin K.W. To; Kwok-Hung Chan; Iris W.S. Li; Tak-Yin Tsang; Herman Tse; Jasper F.W. Chan; Ivan F.N. Hung; Sik-To Lai; Chi-Wai Leung; Yat-Wah Kwan; Yu-Lung Lau; Tak-Keung Ng; Vincent C.C. Cheng; Joseph S.M. Peiris; Kwok-Yung Yuen


Publisher
John Wiley and Sons
Year
2010
Tongue
English
Weight
104 KB
Volume
82
Category
Article
ISSN
0146-6615

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✦ Synopsis


Viral shedding profile of infections caused by the pandemic H1N1 2009 influenza A virus has not been reported. The aim of this study was to determine the viral load in different body sites. Viral loads of pandemic H1N1 virus in respiratory specimens, stool, urine, and serum were determined by quantitative reverse transcriptase-polymerase chain reaction (RT-PCR). Respiratory specimens from patients with seasonal influenza were used as historical controls. Initial pre-treatment viral load were compared between these two groups. Serial respiratory specimens from patients with pandemic H1N1 virus infection were obtained for analysis of viral dynamics. Twenty-two pandemic H1N1 cases and 44 seasonal influenza historical controls were included. The mean initial viral load before oseltamivir therapy was 1.84 x 10(8) copies/ml for pandemic H1N1 virus compared with 3.28 x 10(8) copies/ml in seasonal influenza historical controls (P = 0.085). Among patients with pandemic H1N1 virus infection, peak viral load occurred on the day of onset of symptoms, and declined gradually afterwards, with no virus being detectable in respiratory specimens by RT-PCR 8 days and by culture 5 days after the onset of symptoms respectively, except in one patient. Pandemic H1N1 virus was detected in stool and in urine from 4/9 and 1/14 patients, respectively. Viral culture was also positive from the stool sample with the highest viral load. Younger age was associated with prolonged shedding in the respiratory tract and higher viral load in the stool. Data from this quantitative analysis of viral shedding may have implications for formulating infection control measures.


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