Zhi-Liang Gao

Dr. Zhi-Liang Gao


Research Focus & Metrics

Academic Career Length

15Years (2012-Present)

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

Representative Publications

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1 October 2020 in Cell
Verified
Journal Article
Closed access
QZQiyi Zhao
Qiyi Zhao
JLJiayu Liu
Jiayu Liu
HDHong Deng
Hong Deng
RMRuiying Ma
Ruiying Ma
JLJian-You Liao
Jian-You Liao
SSShicheng Su
Shicheng Su

30 April 2020 in Journal of Medical Virology
Verified
Journal Article
Closed access
PDF file
LPLiang Peng
Liang Peng
JLJing Liu
Jing Liu
WXWenxiong Xu
Wenxiong Xu
QLQiumin Luo
Qiumin Luo
DCDabiao Chen
Dabiao Chen
ZGZhi-Liang Gao
Zhi-Liang Gao

1 May 2020 in Travel Medicine and Infectious Disease
Verified
Journal Article
Open access
ZLZiying Lei
Ziying Lei
HCHuijuan Cao
Huijuan Cao
YJYusheng Jie
Yusheng Jie
ZHZhanlian Huang
Zhanlian Huang
XGXiaoyan Guo
Xiaoyan Guo
BLBing-Liang Lin
Bing-Liang Lin
Coronavirus disease 2019 (COVID-19) has spread outside the initial epicenter of Wuhan. We compared cases in Guangzhou and Wuhan to illustrate potential changes in pathogenicity and epidemiological characteristics as the epidemic has progressed. We studied 20 patients admitted to the Third Affiliated Hospital of Sun Yat-Sen University in Guangzhou, China from January 22 to February 12, 2020. Data were extracted from medical records. These cases were compared with the 99 cases, previously published in Lancet, from Wuhan Jinyintan Hospital from January 1 to January 20, 2020. Guangzhou patients were younger and had better prognosis than Wuhan patients. The Wuhan patients were more likely to be admitted to the ICU (23% vs 5%) and had a higher mortality rate (11% vs 0%). Cases in Guangzhou tended to be more community clustered. Diarrhea and vomiting were more common among Guangzhou patients and SARS-CoV-2 RNA was found in feces. Fecal SARA-CoV-2 RNA remained positive when nasopharyngeal swabs turned negative in some patients. This study indicates possible diminishing virulence of the virus in the process of transmission. Yet persistent positive RNA in feces after negative nasopharyngeal swabs suggests a possible prolonged transmission period that challenges current quarantine practices.

1 January 2021 in Gut Microbes
Verified
Journal Article
Open access
KWKe Wang
Ke Wang
ZZZhao Zhang
Zhao Zhang
ZMZhi-Shuo Mo
Zhi-Shuo Mo
XYXiao-Hua Yang
Xiao-Hua Yang
BLBing-Liang Lin
Bing-Liang Lin
ZGZhi-Liang Gao
Zhi-Liang Gao
The gut microbiota in the hepatitis B virus related acute-on-chronic liver failure (HBV-ACLF) is poorly defined. We aim to uncover the characteristics of the gut microbiota in HBV-ACLF and in other HBV associated pathologies. We analyzed the gut microbiome in patients with HBV-ACLF or other HBV associated pathologies and healthy individuals by 16S rRNA sequencing and metagenomic sequencing of fecal samples. 212 patients with HBV-ACLF, 252 with chronic hepatitis B (CHB), 162 with HBV-associated cirrhosis (HBV-LC) and 877 healthy individuals were recruited for the study. CHB and HBV-LC patients are grouped as HBV-Other. We discovered striking differences in the microbiome diversity between the HBV-ACLF, HBV-Other and healthy groups using 16S rRNA sequencing. The ratio of cocci to bacilli was significantly elevated in the HBV-ACLF group compared with healthy group. Further analysis within the HBV-ACLF group identified 52 genera showing distinct richness within the group where Enterococcus was enriched in the progression group whilst Faecalibacterium was enriched in the regression group. Metagenomic sequencing validated these findings and further uncovered an enrichment of Lactobacillus casei paracasei in progression group, while Alistipes senegalensis, Faecalibacterium prausnitzii and Parabacteroides merdae dominated the regression group. Importantly, our analysis revealed that there was a rapid increase of Enterococcus faecium during the progression of HBV-ACLF. The gut microbiota displayed distinct composition at different phases of HBV-ACLF. High abundance of Enterococcus is associated with progression while that of Faecalibacterium is associated with regression of HBV-ACLF. Therefore, the microbiota features hold promising potential as prognostic markers for HBV-ACLF.

4 February 2019 in Stem Cells International
Verified
Journal Article
Open access
PDF file
WXWenxiong Xu
Wenxiong Xu
HHHong-Liang He
Hong-Liang He
SPShun-Wen Pan
Shun-Wen Pan
YCYuan-Li Chen
Yuan-Li Chen
MZMei-Ling Zhang
Mei-Ling Zhang
JLJianguo Li
Jianguo Li
Background. Hepatitis B virus-related acute-on-chronic liver failure (HBV-ACLF) is a common type of liver failure with a high mortality. This study aimed at investigating the safety and efficacy of the combination treatment of plasma exchange (PE) and umbilical cord-derived mesenchymal stem cell (UC-MSCs) transplantation for HBV-ACLF patients.Methods. A total of 110 HBV-ACLF patients treated in our hospital from January 2012 to September 2017 were enrolled into this trial and divided into the control group (n=30), UC-MSC group (n=30), PE group (n=30), and UC-MSC + PE group (n=20) based on their treatments. The hepatic function, coagulation, and virological and immunological markers were assessed at baseline and 30, 60, 90, 180, and 360 days. The endpoint outcomes were death and unfavorable outcome (need for liver transplantation or death).Results. The UC-MSC + PE group had the lowest rates of death and unfavorable outcome at 30 days, 60 days, and 90 days posttreatment among the four groups, but the difference did not reach significances. The multivariate logistic regression analysis demonstrated that hemoglobin, prothrombin activity, and MELD (model for end-stage liver disease) score were the independent factors associated with the unfavorable outcome (allP<0.05). The levels of total bilirubin, alanine aminotransferase, aspartate transaminase, and MELD score were significantly decreased during treatments (allP<0.05).Conclusion. UC-MSCs combined with PE treatment had good safety but cannot significantly improve the short-term prognosis of HBV-ACLF patients with as compared with the single treatment. The long-term efficacy should be further evaluated. This trial is registered with registration no.NCT01724398.

29 August 2023 in Alimentary Pharmacology & Therapeutics
Verified
Journal Article
Closed access
NGNa Gao
Na Gao
GGGuiwen Guan
Guiwen Guan
GXGanlin Xu
Ganlin Xu
HWHaishi Wu
Haishi Wu
CXChan Xie
Chan Xie
ZGZhi-Liang Gao
Zhi-Liang Gao