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Volume 11, Number 3—March 2005

Dispatch

SARS-associated Coronavirus Transmitted from Human to Pig

Weijun Chen*†1, Minghua Yan‡1, Ling Yang*1, Boliang Ding‡, Bo He†, Yingzhen Wang‡, Xiuli Liu‡, Chenhui Liu*, Hui Zhu‡, Bo You†, Shengyong Huang†, Jiangguo Zhang*, Feng Mu*†, Zhao Xiang*§, Xiaoli Feng*, Jie Wen*†, Jianqiu Fang*†, Jun Yu*, Huanming Yang*, and Jian Wang*†Comments to Author 
Author affiliations: *Chinese Academy of Sciences, Beijing, China; †Beijing BGI-GBI Biotech Co., Ltd, Beijing, China; ‡Tianjin Institute of Animal Husbandry and Veterinary Science, Tianjin, China; §BGI Hangzhou Bio-Environment Technology Co., Ltd, Hangzhou, China; 1W. Chen, M. Yan, and L. Yang contributed equally to this article.

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Figure 1

Detection of antibodies against severe acute respiratory syndrome (SARS)–associated coronavirus recombinant proteins in animal sera by Western blotting. Recombinant nuleocapsid protein in panel A (NP, 54 kilodaltons [kDa]) and partial spike protein in panel B (SP, 57 kDa) were used as antigens. Goat anti-swine immunoglobulin G horseradish peroxidase was used as a secondary antibody. Serum samples from a convalescent SARS patient and healthy persons were used as positive and negative controls, re

Figure 1. . . Detection of antibodies against severe acute respiratory syndrome (SARS)–associated coronavirus recombinant proteins in animal sera by Western blotting. Recombinant nuleocapsid protein in panel A (NP, 54 kilodaltons [kDa]) and partial spike protein in panel B (SP, 57 kDa) were used as antigens. Goat anti-swine immunoglobulin G horseradish peroxidase was used as a secondary antibody. Serum samples from a convalescent SARS patient and healthy persons were used as positive and negative controls, respectively. Swine (S1 to S8) and human (H1 and H2) samples are sera collected during the survey. M1, M2, and M3 are purified NP, SP, and molecular weight markers, respectively. Positive bands at the corresponding molecular weight of the 2 proteins are indicated with arrows.

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