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Detection of SARS Coronavirus in Patients with Suspected SARS

Kwok Hung ChanQueen Mary Hospital, Hong Kong Special Administrative Region, People’s Republic of China (SAR)Leo L. M. PoonUniversity of Hong Kong, Hong Kong SARVincent Chi‐Chung ChengQueen Mary Hospital, Hong Kong Special Administrative Region, People’s Republic of China (SAR)Yi GuanUniversity of Hong Kong, Hong Kong SARIvan Fan‐Ngai HungQueen Mary Hospital, Hong Kong Special Administrative Region, People’s Republic of China (SAR)James H.B. KongHospital Authority Head Office, Hong Kong SARLoretta Yin-Chun YamPamela Youde Nethersole Eastern Hospital, Hong Kong SARWH SetoQueen Mary Hospital, Hong Kong Special Administrative Region, People’s Republic of China (SAR)Kwok‐Yung YuenUniversity of Hong Kong, Hong Kong SARJoseph S. Malik PeirisUniversity of Hong Kong, Hong Kong SAR
2004en
ABI

Аннотация

Cases of severe acute respiratory syndrome (SARS) were investigated for SARS coronavirus (SARS-CoV) through RNA tests, serologic response, and viral culture. Of 537 specimens from patients in whom SARS was clinically diagnosed, 332 (60%) had SARS-CoV RNA in one or more clinical specimens, compared with 1 (0.3%) of 332 samples from controls. Of 417 patients with clinical SARS from whom paired serum samples were available, 92% had an antibody response. Rates of viral RNA positivity increased progressively and peaked at day 11 after onset of illness. Although viral RNA remained detectable in respiratory secretions and stool and urine specimens for >30 days in some patients, virus could not be cultured after week 3 of illness. Nasopharyngeal aspirates, throat swabs, or sputum samples were the most useful clinical specimens in the first 5 days of illness, but later in the illness viral RNA could be detected more readily in stool specimens.

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