George F. Fu Gao

Dr. George F. Fu Gao


Research Focus & Metrics

Academic Career Length

24Years (2003-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

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20 February 2020 in New England Journal of Medicine
Verified
Journal Article
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NZNa Zhu
Na Zhu
DZDingyu Zhang
Dingyu Zhang
WWWenling Wang
Wenling Wang
XLXingwang Li
Xingwang Li
BYBo Yang
Bo Yang
WTWenjie Tan
Wenjie Tan
In December 2019, a cluster of patients with pneumonia of unknown cause was linked to a seafood wholesale market in Wuhan, China. A previously unknown betacoronavirus was discovered through the use of unbiased sequencing in samples from patients with pneumonia. Human airway epithelial cells were used to isolate a novel coronavirus, named 2019-nCoV, which formed another clade within the subgenus sarbecovirus, Orthocoronavirinae subfamily. Different from both MERS-CoV and SARS-CoV, 2019-nCoV is the seventh member of the family of coronaviruses that infect humans. Enhanced surveillance and further investigation are ongoing. (Funded by the National Key Research and Development Program of China and the National Major Project for Control and Prevention of Infectious Disease in China.)

1 June 2016 in Trends in Microbiology
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Journal Article
Closed access
SSShuo Su
Shuo Su
GWGary Wong
Gary Wong
WSWeifeng Shi
Weifeng Shi
JLJun Liu
Jun Liu
ALAlexander C.K. Lai
Alexander C.K. Lai
GGGeorge F. Fu Gao
George F. Fu Gao

26 May 2020 in Nature
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Journal Article
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RSRui Shi
Rui Shi
CSChao Shan
Chao Shan
XDXiaomin Duan
Xiaomin Duan
ZCZhihai Chen
Zhihai Chen
PLPeipei Liu
Peipei Liu
JYJinghua Yan
Jinghua Yan

12 June 2020 in Science
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Journal Article
Open access
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YWYan Wu
Yan Wu
FWFeiran Wang
Feiran Wang
CSChenguang Shen
Chenguang Shen
WPWeiyu Peng
Weiyu Peng
DLDelin Li
Delin Li
LLLei Liu
Lei Liu
An antibody defense against COVID-19: One of the responses of the immune system to invading viruses is the production of antibodies. Some of these are neutralizing, meaning that they prevent the virus from being infectious, and can thus be used to treat viral diseases. Wu et al. isolated four neutralizing antibodies from a convalescent coronavirus disease 2019 (COVID-19) patient. Two of the antibodies, B38 and H4, blocked the receptor binding domain (RBD) of the viral spike protein from binding to the cellular receptor, angiotensin-converting enzyme 2 (ACE2). The structure of the RBD bound to B38 shows that the B38-binding site overlaps with the binding site for ACE2. Although H4 also blocks RBD binding to ACE2, it binds at a different site, and thus the two antibodies can bind simultaneously. This pair of antibodies could potentially be used together in clinical applications. Science , this issue p. 1274

13 June 2007 in PLOS ONE
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Journal Article
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Kegong TianKegong Tian
Kegong Tian
XYXiuling Yu
Xiuling Yu
TZTiezhu Zhao
Tiezhu Zhao
YFYoujun Feng
Youjun Feng
ZCZhen Cao
Zhen Cao
GGGeorge F. Fu Gao
George F. Fu Gao
Porcine reproductive and respiratory syndrome (PRRS) is a severe viral disease in pigs, causing great economic losses worldwide each year. The causative agent of the disease, PRRS virus (PRRSV), is a member of the family Arteriviridae. Here we report our investigation of the unparalleled large-scale outbreaks of an originally unknown, but so-called “high fever” disease in China in 2006 with the essence of PRRS, which spread to more than 10 provinces (autonomous cities or regions) and affected over 2,000,000 pigs with about 400,000 fatal cases. Different from the typical PRRS, numerous adult sows were also infected by the “high fever” disease. This atypical PRRS pandemic was initially identified as a hog cholera-like disease manifesting neurological symptoms (e.g., shivering), high fever (40–42°C), erythematous blanching rash, etc. Autopsies combined with immunological analyses clearly showed that multiple organs were infected by highly pathogenic PRRSVs with severe pathological changes observed. Whole-genome analysis of the isolated viruses revealed that these PRRSV isolates are grouped into Type II and are highly homologous to HB-1, a Chinese strain of PRRSV (96.5% nucleotide identity). More importantly, we observed a unique molecular hallmark in these viral isolates, namely a discontinuous deletion of 30 amino acids in nonstructural protein 2 (NSP2). Taken together, this is the first comprehensive report documenting the 2006 epidemic of atypical PRRS outbreak in China and identifying the 30 amino-acid deletion in NSP2, a novel determining factor for virulence which may be implicated in the high pathogenicity of PRRSV, and will stimulate further study by using the infectious cDNA clone technique.

18 December 2020 in Nature Reviews Immunology
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Journal Article
Closed access
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LDLianpan Dai
Lianpan Dai
GGGeorge F. Fu Gao
George F. Fu Gao