Tianfei Yu

Dr. Tianfei Yu

Qiqihar university
orcid

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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25 August 2023 in BMC Cancer
Verified
Journal Article
Open access
PDF file
MLMing Li
Ming Li
QGQian Gao
Qian Gao
TYTianfei Yu
Tianfei Yu
Background: In research designs that rely on observational ratings provided by two raters, assessing inter-rater reliability (IRR) is a frequently required task. However, some studies fall short in properly utilizing statistical procedures, omitting essential information necessary for interpreting their findings, or inadequately addressing the impact of IRR on subsequent analyses’ statistical power for hypothesis testing. Methods: This article delves into the recent publication by Liu et al. in BMC Cancer, analyzing the controversy surrounding the Kappa statistic and methodological issues concerning the assessment of IRR. The primary focus is on the appropriate selection of Kappa statistics, as well as the computation, interpretation, and reporting of two frequently used IRR statistics when there are two raters involved. Results: The Cohen’s Kappa statistic is typically utilized to assess the level of agreement between two raters when there are two categories or for unordered categorical variables with three or more categories. On the other hand, when it comes to evaluating the degree of agreement between two raters for ordered categorical variables comprising three or more categories, the weighted Kappa is a widely used measure. Conclusion: Despite not substantially affecting the findings of Liu et al.?s study, the statistical dispute underscores the significance of employing suitable statistical methods. Rigorous and accurate statistical results are crucial for producing trustworthy research.

23 August 2019 in Viruses
Verified
Journal Article
Open access
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HYHai-Chang Yin
Hai-Chang Yin
SSShu-Li Shao
Shu-Li Shao
XJXin-Jie Jiang
Xin-Jie Jiang
PXPeng-Yu Xie
Peng-Yu Xie
WSWan-Shu Sun
Wan-Shu Sun
TYTianfei Yu
Tianfei Yu
Autophagy is a catabolic biological process in the body. By targeting exogenous microorganisms and aged intracellular proteins and organelles and sending them to the lysosome for phagocytosis and degradation, autophagy contributes to energy recycling. When cells are stimulated by exogenous pathogenic microorganisms such as viruses, activation or inhibition of autophagy is often triggered. As autophagy has antiviral effects, many viruses may escape and resist the process by encoding viral proteins. At the same time, viruses can also use autophagy to enhance their replication or increase the persistence of latent infections. Here, we give a brief overview of autophagy and DNA viruses and comprehensively review the known interactions between human and animal DNA viruses and autophagy and the role and mechanisms of autophagy in viral DNA replication and DNA virus-induced innate and acquired immunity.

29 July 2022 in Parasites & Vectors
Verified
Journal Article
Open access
PDF file
MLMing Li
Ming Li
TYTianfei Yu
Tianfei Yu
We read with great interest the article by Hendershot et al. (Parasit Vectors 14:473, 2021). The authors compared a PCR method for detecting Plasmodium vivax’s mitochondrial (mt) cytochrome oxidase I (COX-I) gene with the current “gold standard” circumsporozoite (CSP) ELISA for detecting circumsporozoite protein for identification of different life stages of Plasmodium vivax during development within Anopheles arabiensis. We found that Cohen’s kappa value for measuring the agreement between mt COX-I PCR and CSP ELISA was questionable. In addition, we recommend a more appropriate statistical method in this article.In short, any scientific conclusion requires support by the reasonable application of methodological and statistical methods.

3 October 2022 in Microbiome
Verified
Journal Article
Open access
PDF file
HYHai-Chang Yin
Hai-Chang Yin
ZLZhen-Dong Liu
Zhen-Dong Liu
WZWei-Wei Zhang
Wei-Wei Zhang
QYQing-Zhu Yang
Qing-Zhu Yang
TYTianfei Yu
Tianfei Yu
QMQING MENG
QING MENG
Background: Mammalian intestinal microbiomes are necessary for antagonizing systemic viral infections. However, very few studies have identified whether poultry commensal bacteria play a crucial role in protecting against systemic viral infections. Nephropathogenic infectious bronchitis virus (IBV) is a pathogenic coronavirus that causes high morbidity and multiorgan infection tropism in chickens. Results: In this study, we used broad-spectrum oral antibiotics (ABX) to treat specific pathogen free (SPF) chickens to deplete the microbiota before infection with nephropathogenic IBV to analyze the impact of microbiota on IBV infections in vivo. Depletion of the SPF chicken microbiota increases pathogenicity and viral burden following IBV infection. The gnotobiotic chicken infection model further demonstrated that intestinal microbes are resistant to nephropathogenic IBV infection. In addition, ABX-treated chickens showed a severe reduction in macrophage activation, impaired type I IFN production, and IFN-stimulated gene expression in peripheral blood mononuclear cells and the spleen. Lactobacillus isolated from SPF chickens could restore microbiota-depleted chicken macrophage activation and the IFNAR-dependent type I IFN response to limit IBV infection. Furthermore, exopolysaccharide metabolites of Lactobacillus spp. could induce IFN-β. Conclusions: This study revealed the resistance mechanism of SPF chicken intestinal microbiota to nephropathogenic IBV infection, providing new ideas for preventing and controlling nephropathogenic IBV.


1 January 2013 in Brazilian Journal of Microbiology
Verified
Journal Article
Open access
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MLMing Li
Ming Li
TYTianfei Yu
Tianfei Yu
Through bioinformatic prediction, between Muscovy duck parvovirus (MDPV) and goose parvovirus (GPV), there were one epitope AA503–509 (RANEPKE) on non-structural protein and three epitopes AA426–430 (SQDLD), 540–544 (DPYRS), 685–691 (KENSKRW) on structural protein might cross-react with each other. Furthermore, the four epitops were expressed in Escherichia coli. All the four recombinant proteins could react with GPV-antisera and MDPV-antisera in Western blot.