1.Research progress in active substances and their mechanisms of action against porcine epidemic diarrhea virus.
Yu LIU ; Sisi SU ; Ziqian WANG ; Jiahao WU ; Hongwei CHEN ; Hongzao YANG
Chinese Journal of Biotechnology 2025;41(7):2519-2533
Porcine epidemic diarrhea virus (PEDV) is an intestinal coronavirus that can cause porcine epidemic diarrhea, leading to diarrhea, vomiting, weight loss, and even death in piglets. Due to the diversity of PEDV strains, traditional vaccines are difficult to sustainably and effectively prevent and control PEDV. This article reviews the strategies and mechanisms of active substances in regulating intracellular signaling pathways, viral proteins, and microbial metabolites to enhance the host immune function against PEDV. It emphasizes the prevention of PEDV resistance and the potential harm of PEDV breaking through interspecies barriers to the human society, aiming to provide reliable theoretical support for the development of new antiviral drugs or vaccines.
Porcine epidemic diarrhea virus/immunology*
;
Animals
;
Swine
;
Swine Diseases/prevention & control*
;
Antiviral Agents/pharmacology*
;
Coronavirus Infections/virology*
;
Viral Vaccines/immunology*
;
Humans
;
Signal Transduction
2.A truncated N protein-based ELISA method for the detection of antibodies against porcine deltacoronavirus.
Dongsheng WANG ; Ruiming YU ; Liping ZHANG ; Yingjie BAI ; Xia LIU ; Yonglu WANG ; Xiaohua DU ; Xinsheng LIU
Chinese Journal of Biotechnology 2025;41(7):2760-2773
This study aims to establish an antibody detection method for porcine deltacoronavirus (PDCoV). The recombinant proteins PDCoV-N1 and PDCoV-N2 were expressed via the prokaryotic plasmid pColdII harboring the N gene sequence of the PDCoV strain CH/XJYN/2016. The reactivity and specificity of PDCoV-N1 and PDCoV-N2 with anti-PEDV sera were analyzed after the recombinant proteins were analyzed by SDS-PAGE and purified by the Ni-NTA Superflow Cartridge. Meanwhile, Western blotting and indirect immunofluorescence assay were carried out separately to validate the recombinant proteins PDCoV-N1 and PDCoV-N2. Finally, we established an indirect ELISA method based on the recombinant protein PDCoV-N2 after optimizing the conditions and tested the sensitivity, specificity, and reproducibility of the method. Then, the established method was employed to examine 102 clinical serum samples. The recombinant protein PDCoV-N2 showed low cross-reactivity with anti-PEDV sera. The optimal conditions of the indirect ELISA method based on PDCoV-N2 were as follows: the antigen coating concentration of 1.25 μg/mL and coating at 37 ℃ for 1 h; blocking by BSA overnight at 4 ℃; serum sample dilution at 1:50 and incubation at 37 ℃ for 1 h; secondary antibody dilution at 1:80 000 and incubation at 37 ℃ for 1 h; color development with TMB chromogenic solution at 37 ℃ for 10 min. The S/P value ≥ 0.45, ≤0.38, and between 0.45 and 0.38 indicated that the test sample was positive, negative, and suspicious, respectively. The testing results of the antisera against porcine epidemic diarrhea virus (PEDV), porcine circovirus 2 (PCV2), transmissible gastroenteritis virus (TGEV), foot-and-mouth disease virus (FMDV), and African swine fever virus (ASFV) showed that the S/P values were all less than 0.38. The testing results of the 800-fold diluted anti-PDCoV sera were still positive. The results of the inter- and intra-batch tests showed that the coefficients of variation of this method were less than 10%. Clinical serum sample test results showed the coincidence rate between this method and neutralization test was 94.12%. In this study, an ELISA method for the detection of anti-PDCoV antibodies was successfully established based on the truncated N protein of PDCoV. This method is sensitive, specific, stable, and reproducible, serving as a new method for the clinical diagnosis of PDCoV.
Animals
;
Enzyme-Linked Immunosorbent Assay/methods*
;
Swine
;
Antibodies, Viral/blood*
;
Recombinant Proteins/genetics*
;
Deltacoronavirus/isolation & purification*
;
Coronavirus Infections/virology*
;
Swine Diseases/diagnosis*
;
Coronavirus Nucleocapsid Proteins
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Sensitivity and Specificity
4.Analysis of an improved workflow of endoscope reprocessing for bedside endoscopic diagnosis and treatment on COVID-19 patients.
Qing GU ; Hua-Fen WANG ; Ying FANG ; Ye LU ; Zhe SHEN ; Yan WANG ; Xin WU ; Li CEN ; Yi-Shu CHEN
Journal of Zhejiang University. Science. B 2020;21(5):416-422
Severe cases infected with the coronavirus disease 2019 (COVID-19), named by the World Health Organization (WHO) on Feb. 11, 2020, tend to present a hypercatabolic state because of severe systemic consumption, and are susceptible to stress ulcers and even life-threatening gastrointestinal bleeding. Endoscopic diagnosis and treatment constitute an irreplaceable part in the handling of severe COVID-19 cases. Endoscopes, as reusable precision instruments with complicated structures, require more techniques than other medical devices in cleaning, disinfection, sterilization, and other reprocessing procedures. From 2016 to 2019, health care-acquired infection caused by improper endoscope reprocessing has always been among the top 5 on the list of top 10 health technology hazards issued by the Emergency Care Research Institute. Considering the highly infective nature of COVID-19 and the potential aerosol contamination therefrom, it is of pivotal significance to ensure that endoscopes are strictly reprocessed between uses. In accordance with the national standard "Regulation for Cleaning and Disinfection Technique of Flexible Endoscope (WS507-2016)," we improved the workflow of endoscope reprocessing including the selection of chemicals in an effort to ensure quality control throughout the clinical management towards COVID-19 patients. Based on the experience we attained from the 12 severe COVID-19 cases in our hospital who underwent endoscopy 23 times in total, the article provides an improved version of endoscopic reprocessing guidelines for bedside endoscopic diagnosis and treatment on COVID-19 patients for reference.
Adult
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Aged
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Aged, 80 and over
;
Betacoronavirus
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China
;
Coronavirus Infections
;
diagnosis
;
therapy
;
Cross Infection
;
prevention & control
;
Disinfection
;
methods
;
Endoscopes
;
virology
;
Equipment Contamination
;
prevention & control
;
Female
;
Humans
;
Male
;
Middle Aged
;
Pandemics
;
Peracetic Acid
;
Personal Protective Equipment
;
Pneumonia, Viral
;
diagnosis
;
therapy
;
Sterilization
;
methods
;
Workflow
5.Primary percutaneous coronary intervention in a COVID-19 patient with ST-segment elevation myocardial infarction after lung transplantation: a case report.
Tian-Ming XUAN ; Xing-Xiang WANG ; Xiang-Yuan PU ; Wei-Li HAN ; Xiao-Gang GUO
Journal of Zhejiang University. Science. B 2020;21(5):411-415
We present an unusual case of a patient with bilateral-lung transplantation due to severe coronavirus disease 2019 (COVID-19), who subsequently suffered complications with acute myocardial infarction and underwent primary percutaneous coronary intervention (PCI).
Aged
;
Betacoronavirus
;
China
;
Coronavirus Infections
;
complications
;
Humans
;
Lung Diseases
;
surgery
;
virology
;
Lung Transplantation
;
Male
;
Pandemics
;
Percutaneous Coronary Intervention
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Pneumonia, Viral
;
complications
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ST Elevation Myocardial Infarction
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surgery
;
virology
6.Transmission risk of patients with COVID-19 meeting discharge criteria should be interpreted with caution.
Jun-Wei SU ; Wen-Rui WU ; Guan-Jing LANG ; Hong ZHAO ; Ji-Fang SHENG
Journal of Zhejiang University. Science. B 2020;21(5):408-410
As of Apr. 22, 2020, the World Health Organization (2020) has reported over 2.4 million confirmed coronavirus disease 2019 (COVID-19) patients and 169 151 deaths. Recent articles have uncovered genomic characteristics and clinical features of COVID-19 (Chan et al., 2020; Chang et al., 2020; Guan et al., 2020; Zhu et al., 2020), while our understanding of COVID-19 is still limited. As suggested by guidelines promoted by the General Office of National Health Commission of the People's Republic of China (2020) (from Versions 1 to 6), discharged standards for COVID-19 were still dependent on viral real-time polymerase chain reaction (RT-PCR) tests of respiratory specimens, showing that recovered COVID-19 patients with twice negative RT-PCR could meet discharge criteria. Here, we examined two cases in which nucleic acid test results were inconsistent with clinical and radiological findings, leading to suboptimal care.
Adult
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Betacoronavirus
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China
;
Clinical Laboratory Techniques
;
Coronavirus Infections
;
diagnosis
;
transmission
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Female
;
Humans
;
Male
;
Middle Aged
;
Pandemics
;
Patient Discharge
;
Pneumonia, Viral
;
diagnosis
;
transmission
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Real-Time Polymerase Chain Reaction
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Reverse Transcriptase Polymerase Chain Reaction
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Sputum
;
virology
7.Can SARS-CoV-2-infected women breastfeed after viral clearance?
Journal of Zhejiang University. Science. B 2020;21(5):405-407
The recently emerged novel coronavirus pneumonia, named the coronavirus disease 2019 (COVID-19), shares several clinical characteristics with severe acute respiratory syndrome (SARS) and Middle East respiratory syndrome (MERS), and spread rapidly throughout China in December of 2019 (Huang et al., 2020). The pathogen 2019 novel coronavirus (2019-nCoV) is now named SARS coronavirus 2 (SARS-CoV-2) and is highly infectious. As of Apr. 9, 2020, over 80 000 confirmed cases had been reported, with an estimated mortality rate of 4.0% (Chinese Center for Disease Control and Prevention, 2020). Person-to-person transmission and familial clustering have been reported (Chan et al., 2020; Nishiura et al., 2020; Phan et al., 2020). However, there is no evidence of fetal intrauterine infection in pregnant women who have been infected with SARS-CoV-2 in their third trimester (Chen et al., 2020). It is unclear whether breastfeeding transmits the virus from previously infected and recovered mothers to their babies. Here we report the clinical course of a pregnant woman with COVID-19. In order to determine whether SARS-CoV-2 can be transmitted to newborns through breastfeeding, we measured viral RNA in the patient's breastmilk samples at different time points after delivery.
Adult
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Betacoronavirus
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Breast Feeding
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China
;
Coronavirus Infections
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diagnosis
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Female
;
Humans
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Infant, Newborn
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Infectious Disease Transmission, Vertical
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Milk, Human
;
virology
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Pandemics
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Pneumonia, Viral
;
diagnosis
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Pregnancy
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Pregnancy Complications, Infectious
;
virology
;
RNA, Viral
;
isolation & purification
8.Clinical characteristics of 34 COVID-19 patients admitted to intensive care unit in Hangzhou, China.
Yi ZHENG ; Li-Jun SUN ; Mi XU ; Jian PAN ; Yun-Tao ZHANG ; Xue-Ling FANG ; Qiang FANG ; Hong-Liu CAI
Journal of Zhejiang University. Science. B 2020;21(5):378-387
OBJECTIVE:
This study summarizes and compares clinical and laboratory characteristics of 34 patients admitted to the intensive care unit (ICU) for complications from coronavirus disease 2019 (COVID-19) at the First Affiliated Hospital, School of Medicine, Zhejiang University, Hangzhou, China from Jan. 22 to Mar. 5, 2020.
METHODS:
A total of 34 patients were divided into two groups, including those who required noninvasive ventilation (NIV) and invasive mechanical ventilation (IMV) with additional extracorporeal membrane oxygenation (ECMO) in 11 patients. Clinical features of COVID-19 patients were described and the parameters of clinical characteristics between the two groups were compared.
RESULTS:
The rates of the acute cardiac and kidney complications were higher in IMV cases than those in NIV cases. Most patients had lymphocytopenia on admission, with lymphocyte levels dropping progressively on the following days, and the more severe lymphopenia developed in the IMV group. In both groups, T lymphocyte counts were below typical lower limit norms compared to B lymphocytes. On admission, both groups had higher than expected amounts of plasma interleukin-6 (IL-6), which over time declined more in NIV patients. The prothrombin time was increased and the levels of platelet, hemoglobin, blood urea nitrogen (BUN), D-dimer, lactate dehydrogenase (LDH), and IL-6 were higher in IMV cases compared with NIV cases during hospitalization.
CONCLUSIONS
Data showed that the rates of complications, dynamics of lymphocytopenia, and changes in levels of platelet, hemoglobin, BUN, D-dimer, LDH and IL-6, and prothrombin time in these ICU patients were significantly different between IMV and NIV cases.
Acute Kidney Injury
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virology
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Aged
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Aged, 80 and over
;
Betacoronavirus
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Blood Urea Nitrogen
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China
;
Coronavirus Infections
;
complications
;
therapy
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Extracorporeal Membrane Oxygenation
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Female
;
Fibrin Fibrinogen Degradation Products
;
analysis
;
Heart Diseases
;
virology
;
Hemoglobins
;
analysis
;
Hospitalization
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Humans
;
Intensive Care Units
;
Interleukin-6
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blood
;
L-Lactate Dehydrogenase
;
blood
;
Lymphopenia
;
virology
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Male
;
Middle Aged
;
Noninvasive Ventilation
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Pandemics
;
Pneumonia, Viral
;
complications
;
therapy
;
Positive-Pressure Respiration
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Prothrombin Time
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Retrospective Studies
9.The 40-91 aa sequence of porcine epidemic diarrhea virus ORF3 protein is the key structural domain controlling its location in cytoplasm.
Bingqing CHEN ; Mei SHEN ; Fusheng SI ; ShiJuan DONG ; RuiSong YU ; ChunFang XIE ; Zhen LI
Chinese Journal of Biotechnology 2020;36(6):1113-1125
ORF3 protein, the single accessory protein encoded by porcine epidemic diarrhea virus (PEDV), is related to viral pathogenicity. In order to determine the cytoplasmic location signal of PEDV ORF3, we constructed a series of recombinant plasmids carrying full-length or truncated segments of PEDV DR13 ORF3 protein. When the acquired plasmids were transfected into Vero cells, expression and distribution of the EGFP-fused full-length ORF3 protein and its truncated forms in the cells were observed by laser confocal microscopy. The results showed that ORF3 protein or their truncated forms containing 40-91 aa segment including two transmembrane domains were localized in the cytoplasm, whereas ORF3 truncated peptides without the 40-91 aa segment were distributed in the whole cell (in both cytoplasm and nucleus). This suggests that the 40-91 aa is the key structural domain determining cytoplasmic location of PEDV ORF3 protein. The discovery provides reference for further clarifying intracellular transport and biological function of PEDV ORF3 protein.
Amino Acid Sequence
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Animals
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Chlorocebus aethiops
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Coronavirus Infections
;
virology
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Cytoplasm
;
virology
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Porcine epidemic diarrhea virus
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genetics
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Protein Domains
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Swine
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Vero Cells
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Viral Proteins
;
chemistry
;
metabolism
10.Optimization of a fluorescent qPCR detection for RNA of SARS-CoV-2.
Xuelong LI ; Junhua LIU ; Qianyang LIU ; Lin YU ; Shanshan WU ; Xiushan YIN
Chinese Journal of Biotechnology 2020;36(4):732-739
We optimized a fluorescent quantitative polymerase chain reaction (qPCR) assay system for rapid and real time detection of SARS-CoV-2 RNA. The results show that the lowest dilution of RNA samples used for the detection of SARS-CoV-2 RNA could reach 1/10 000 (the initial value is set as 10 ng/μL). Moreover, the cycle threshold (Ct) for samples of clinically diagnosed COVID-19 was lower than 35 or 40. The sensitivity of this method was satisfactory. The results were consistent with those of the COVID-19 detection kit on the market under the same conditions, but the number of cycles required was shortened by about 2. Therefore, the optimized assay developed in this study can be used in screening and early clinical diagnosis. Our work provides a tool to facilitate rapid clinical diagnosis of COVID-19.
Betacoronavirus
;
genetics
;
isolation & purification
;
Coronavirus Infections
;
diagnosis
;
virology
;
Early Diagnosis
;
Humans
;
Pandemics
;
Pneumonia, Viral
;
diagnosis
;
virology
;
Polymerase Chain Reaction
;
methods
;
standards
;
RNA, Viral
;
analysis
;
genetics
;
Sensitivity and Specificity
;
Time Factors

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