Hepatitis E Virus

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This book systematically and comprehensively discusses the biological, epidemiological, and clinical characteristics of the hepatitis E virus (HEV). It presents current knowledge of HEV and explores experimental methods, treatment, and prevention of HEV. First identified in the 1980s and cloned in 1990, HEV is the causative agent of hepatitis E, which mainly occurs in developing regions, such as Southeast Asia, the Middle East, and Africa, and significantly affects the health of the people in these areas. It is estimated that a third of the world’s population has been infected with HEV, which is transmitted via the fecal-oral route and can infect both humans and animals. 

In the second edition, new chapters are added to demonstrate the lifecycle, morphogenesis, and stem cell culture of hepatitis E virus. Although research on hepatitis E virus has made progress recently, there are still some problems that have not been solved. Those problems are discussed in this edition, which would be helpful for researchers to understand the problems on hepatitis E virus that they have faced. Meanwhile, the epidemiology, transmission, genetic evolution, animal models, treatment, and others in the related chapters of the first version were also updated according to the most recent research progress. 

 The book provides an overview of HEV from benchside to bedside. It is a valuable resource for researchers in the field and those in the pharmaceutical industry developing HEV vaccines, as well as physicians involved in identifying and treating those infected with the virus.


Author(s): Youchun Wang
Series: Advances in Experimental Medicine and Biology, 1417
Edition: 2
Publisher: Springer
Year: 2023

Language: English
Pages: 260
City: Singapore

Preface to the Second Edition
Contents
Editor and Contributors
1: Hepatitis E Virus
1.1 The Discovery of ET-NANBH
1.2 Molecular Cloning of the ET-NANBH Virus Genome
1.3 Classification of HEV
1.4 Structure of the HEV Genome
1.5 Morphological Appearance and Physiochemical Properties of ET-NANB
1.6 Conclusions and Perspective
References
2: Characteristics and Functions of HEV Proteins
2.1 ORF1 Protein
2.1.1 Structural Features of ORF1 Proteins
2.1.2 Expression of ORF1
2.1.3 Virus Infection and Pathogenicity Relevant to ORF1
2.1.4 ORF1 and Virus Replication
2.1.5 ORF1 and Viral Adaption
2.2 ORF2 Protein
2.2.1 Expression of HEV ORF2 Protein
2.2.2 ORF2 Involved in HEV Infection and Intercellular Transduction
2.2.3 ORF2 and the Endoplasmic Reticulum Stress Response (ERSR)
2.2.4 ORF2 Interferes Host Innate Immunity
2.3 ORF3 Protein
2.3.1 Molecular Structure of ORF3 Protein
2.3.2 ORF3 Protein and Host Cell Survival
2.3.3 ORF3 Protein and the Virus Replication Environment
2.3.4 ORF3 Protein and Clinical Symptoms
2.3.5 ORF3 Protein Is Associated with HEV Release
2.4 ORF4 Protein
2.4.1 Features and Expression of ORF4
2.4.2 ORF4 Protein and HEV Replication
2.5 Conclusion
References
3: Epidemiology of Hepatitis E
3.1 Introduction
3.2 Worldwide HEV Serological Prevalence in the Human Population
3.2.1 Difference of HEV Serological Prevalence Between Countries
3.2.2 Difference of HEV Serological Prevalence Between Regions Within a Country
3.2.3 HEV Serological Prevalence Increases with Age in General Populations
3.2.4 The Changing of HEV Seroprevalence over Time
3.3 HEV Genotype Distribution Worldwide
3.3.1 Asia
3.3.2 Africa
3.3.3 America
3.3.4 Europe
3.3.5 Australia and New Zealand
3.4 Epidemiologic Patterns of HEV Infection
3.4.1 The Epidemiologic Pattern of Infection with HEV-1 and HEV-2
3.4.1.1 Reservoirs of HEV-1 and HEV-2
3.4.1.2 Waterborne Outbreaks of Hepatitis E
3.4.1.3 Sporadic Hepatitis E in Hyperendemic Regions
3.4.2 Epidemiologic Pattern of HEV Infection in Industrialized Countries
3.4.3 The Shifting Epidemiology Pattern of Hepatitis E in China
3.5 Hepatitis E Prevention and Control
3.6 Conclusion
References
4: Hepatitis E as a Zoonosis
4.1 Introduction to Zoonotic HEV Infections
4.2 Introduction to HEV Infection in Animals
4.3 Taxonomical Considerations
4.4 Swine HEV
4.5 Wild Boar HEV
4.6 Rabbit HEV
4.7 Avian HEV
4.8 Camelid HEV
4.9 Rat HEV
4.10 Other Animal Species Infected by HEV
4.11 Conclusions
References
5: Genetic Evolution of Hepatitis E Virus
5.1 General Variation
5.2 ORF1 Variation
5.2.1 Common HVR Properties Between Genotypes
5.2.2 Divergence and Variation in the HVR from Various HEV Genotypes
5.2.3 The Relationship Between HVR Variation and HVR Characteristics
5.3 ORF2 Variation
5.3.1 Epitope Analysis of ORF2 Protein
5.3.2 Mutations in Potential Glycosylation Sites
5.3.3 Mutations in the Capsid Protein
5.4 ORF3 Protein
5.4.1 Divergence of ORF3 Genes and Proteins from Various HEV Genotypes
5.4.2 Immunogenicity and Antigenic Epitopes in the ORF3 Protein
5.5 Conclusion
References
6: Transmission of Hepatitis E Virus
6.1 Introduction
6.2 Waterborne Transmission of HEV
6.2.1 Waterborne Transmission of HEV-1 and HEV-2
6.2.2 Waterborne Transmission of HEV-3 and HEV-4
6.2.2.1 Surface Water Contamination and Transmission of HEV
6.2.2.2 Coastal Water Contamination and Transmission of HEV
6.3 Zoonotic Risks and Foodborne Transmission
6.3.1 Known and Potential Animal Reservoirs
6.3.2 Zoonotic Transmission Through Direct Contact with Infected Animals
6.3.3 Animal Derived Foodborne Transmission
6.4 Blood-Borne Transmission of HEV
6.4.1 Seroprevalence and Incidence of HEV Infection in Blood Donors
6.4.2 Transfusion-Acquired Hepatitis E Cases
6.4.3 The Consequences of Transfusion-Transmitted HEV Infection
6.4.4 Hepatitis E Screening for Blood Donations
6.5 HEV Transmission Through Organ Transplantation
6.6 Vertical Transmission of HEV
6.6.1 The Incidence of HEV Infection in Pregnant Women
6.6.2 The Incidence of Vertical HEV Transmission
6.6.3 The Outcome of HEV-Infected Babies
6.7 Conclusion
References
7: Immunobiology and Host Response to HEV
7.1 Innate Immune Responses to HEV
7.1.1 Induction of Apoptosis
7.1.2 Innate Sensing by Toll-Like Receptors (TLRs)
7.1.3 HEV Infection-Mediated IFNs
7.1.4 Activation of NK Cells
7.1.5 Alteration of NF-κB Activity
7.1.6 Alteration of Other Factors in the Innate Immune Responses
7.2 Specific Antibody Responses to HEV
7.2.1 Major Antigenic Determinants
7.2.1.1 Identification of the Immunodominant Region on HEV
7.2.1.2 Critical Role of Correct Folding of the Immunodominant Region in Detecting Anti-HEV Antibodies
7.2.1.3 Essential Role of Dimerization of the Immunodominant Region in Detecting Anti-HEV Antibodies
7.2.2 Antibody Responses to Immunodominant Antigenic Determinants
7.2.2.1 Anti-HEV IgM and IgG Responses in Experimentally Infected Animal Models
7.2.2.2 Anti-HEV IgM and IgG Responses in Naturally Infected Humans
7.2.2.3 Persistence of Anti-HEV IgG
7.2.2.4 Anti-HEV IgA Response
7.2.2.5 Cross-Reactivity and Cross-Protection of Anti-HEV Antibodies to Different Human HEV Genotypes
7.2.2.6 Antibody Responses to Other Antigenic Determinants
7.2.2.7 Rare Events in the Antibody Responses to HEV Infection
7.2.2.8 Significance of Anti-HEV Responses
7.3 Adaptive T-cell Immune Response to HEV
7.4 Conclusion
References
8: HEV Cell Culture
8.1 Introduction
8.2 HEV Cell Culture
8.2.1 Overview of HEV Cell Culture
8.2.2 Sources of Primary Virus Stocks
8.2.3 Host Cells
8.2.4 Impact of Medium Components on HEV Culture
8.3 Genetic Mutation During HEV Passage
8.4 HEV Infectious cDNA Clone
8.5 Applications of Cell Culture
8.5.1 Viral Thermal Stability Studies
8.5.2 HEV Genome Structure and Function Analysis
8.5.3 pORF1 Post-translational Processing and HVR Function Analysis
8.5.4 pORF2 Post-translational Processing and Its Function in Virus Assembly and Determination of Host Range
8.5.5 pORF3 Role in the Envelope Formation and Virus Release
8.5.6 Neutralization Analysis
8.6 Summary and Outlook
References
9: Liver Organoid Potential Application for Hepatitis E Virus Infection
9.1 Introduction
9.2 Overview of HEV Life Cycle
9.3 Organoid as a Model for HEV Infection
9.3.1 What Are Organoids?
9.3.2 Liver Organoid
9.3.3 Liver Organoids Generation
9.3.4 Liver Organoids for Hepatitis Virus Infections
9.3.5 Liver Organoids Potentially for HEV Infection
9.4 Conclusion and Outlook
References
10: Hepatitis E Virus Life Cycle
10.1 Introduction
10.2 Attachment and Entry
10.2.1 Entry of Naked HEV (neHEV)
10.2.2 Entry of Quasi-Enveloped HEV (eHEV)
10.2.3 Methods for Discovery of Functional HEV Receptor(s)
10.3 Translation, Replication, and Transcription
10.3.1 Translation
10.3.2 Replication and Transcription
10.3.2.1 ORF1: The Enzyme Catalyzes the Viral Genome Replication and Transcription
10.3.2.2 Host Factors Regulate Virus Replication and Transcription
10.4 Assembly and Release
10.4.1 ORF2: Viral Capsid Protein
10.4.2 ORF3: The Viroporin Regulating Viral Particles Release
10.5 Summary
References
11: Morphogenesis of Hepatitis E Virus
11.1 The Morphology and Composition of Non-enveloped and Quasi-Enveloped Virions
11.1.1 HEV Particles in Feces Are Non-enveloped
11.1.2 HEV Particles Circulating in the Bloodstream and in Culture Fluid are Associated with Lipid Membrane
11.1.3 The Protein and Lipid Composition in Non-enveloped and Quasi-Enveloped HEV
11.2 The Formation of Naked and Quasi-Enveloped HEV Particles
11.3 Attachment Factors and Receptors Hijacked by Non-enveloped and Quasi-Enveloped HEV
11.3.1 Attachment Factors and Receptors Hijacked by Non-enveloped HEV
11.3.2 Attachment Factors and Receptors Hijacked by Quasi-Enveloped HEV
11.4 The Internalization and Uncoating of Non-enveloped and Quasi-Enveloped HEV
11.4.1 The Internalization of Non-enveloped and Quasi-Enveloped HEV
11.4.2 The Uncoating of Non-enveloped and Quasi-Enveloped HEV
11.5 Potential Roles of Non-enveloped and Quasi-Enveloped HEV in Viral Transmission, Tropism, and Spread
11.5.1 Transmission of Non-enveloped and Quasi-Enveloped HEV
11.5.2 Potential Role of Quasi-Enveloped HEV in Viral Extrahepatic Replication
11.6 Conclusions and Perspectives
References
12: Animal Models for Hepatitis E Virus
12.1 Introduction
12.2 Nonhuman Primate Models
12.2.1 Pathogenesis
12.2.2 Cross-Species Infection
12.2.3 Vaccine Studies
12.3 Rabbit Models
12.3.1 Pathogenesis
12.3.2 Cross-Species Infection
12.3.3 Vaccine Studies and Antiviral Screening
12.4 Pig Models
12.4.1 Pathogenesis
12.4.2 Cross-Species Infection
12.4.3 Vaccine Studies
12.5 Chicken Models
12.5.1 Pathogenesis
12.5.2 Vaccine Study
12.6 Mice with Humanized Liver
12.7 Mongolian Gerbil Models
12.8 Ferret Models
12.9 Conclusion
References
13: Clinical Manifestations of Hepatitis E
13.1 Introduction
13.2 Acute Hepatitis E
13.2.1 Clinical Manifestations
13.2.2 Pathology
13.2.3 Diagnosis
13.3 Chronic Hepatitis E
13.4 Extrahepatic Complications of HEV Infection
13.4.1 Neurological Complications
13.4.2 Thrombocytopenia
13.4.3 Hemolysis
13.5 Other Complications Associated with HEV
13.5.1 Acute Pancreatitis Associated with Hepatitis E
13.5.2 Autoimmune Disorders Associated with HEV Infection
13.5.2.1 Allergic Purpura
13.5.2.2 Nephritis
13.5.2.3 Aplastic Anemia
13.6 Hepatitis E in Pregnant Women
13.6.1 Clinical Features
13.6.2 Treatment and Prevention
13.7 HEV Infection in Neonates
13.8 Special Manifestations
13.9 Conclusion
References
14: Laboratory Diagnosis of HEV Infection
14.1 Dynamic Changes in HEV Markers After HEV Infection
14.2 Clinical Diagnostic Criteria of HEV Infection
14.3 Assays Used in Laboratory Diagnoses
14.3.1 Antigens Used in Antibody Detecting Assays
14.3.2 Anti-HEV IgG, IgM Assays
14.3.3 Total HEV Antibody Assays
14.3.4 HEV Antigen Assays
14.3.5 HEV Nucleic Acids Detecting Assays
14.4 Immunohistochemical Detection of HEV Proteins in Liver Tissue
14.5 Conclusion and Prospective
References
15: Treatment of Hepatitis E
15.1 Acute Hepatitis E Treatment
15.2 Chronic Hepatitis E Treatment
15.2.1 Reduction of Immunosuppressive Medication
15.2.2 Treatment with Ribavirin
15.2.3 Treatment with Pegylated Interferon-α
15.2.4 Treatment with Sofosbuvir
15.2.5 Treatment of Extrahepatic Complications
15.3 Treatment of HEV-Related Cholestatic Hepatitis
15.4 Treatment of HEV-Related Liver Failure
15.4.1 Clinical Assessment, Monitoring, and Standard Care
15.4.2 Supportive Treatment
15.4.3 Etiological Treatment
15.4.4 Prevention and Treatment of Complications
15.4.5 Liver Support Devices
15.4.6 Liver Transplantation
15.5 Evaluation of Antiviral Drugs In Vitro and in Animal Models
15.6 Conclusion
References
16: Prophylactic Hepatitis E Vaccine
16.1 Introduction
16.2 Rationale for Developing a Hepatitis E Vaccine
16.3 Neutralizing Epitopes
16.4 Assembly of Virus-Like Particle
16.5 Hepatitis E Vaccine Candidates
16.5.1 Trp-C2 Protein
16.5.2 56 kDa Proteins
16.5.3 HEV E2 Protein and HEV 239 VLP
16.6 Clinical Trials
16.6.1 56 kDa Vaccine
16.6.2 HEV 239 Vaccine
16.7 Critical Quality Attributes of HEV239 Vaccine
16.7.1 Biochemical Methods
16.7.2 Biophysical Methods
16.7.3 Immunochemical Methods
16.7.4 Immunological Assessment
16.8 Target Populations
References
17: Puzzles for Hepatitis E Virus
17.1 Introduction
17.2 Genome Organization of HEV
17.3 Classification and Animal Hosts of HEV
17.4 Transmission of HEV
17.5 Chronic HEV Infection
17.6 HEV-Associated Extra-Hepatic Manifestations
17.7 Prevention of HEV Infection
17.8 Treatment
17.8.1 Treatment of Acute HEV Infection
17.8.2 Treatment of Chronic HEV Infection
17.9 Conclusion and Perspectives
References