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Chikungunya Virus

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Cover of 'Chikungunya Virus'

Table of Contents

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    Book Overview
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    Chapter 1 Evolution and Epidemiology of Chikungunya Virus
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    Chapter 2 Molecular Epidemiology of Chikungunya Virus by Sequencing
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    Chapter 3 Chikungunya Virus
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    Chapter 4 Synthetic Peptide-Based Antibody Detection for Diagnosis of Chikungunya Infection with and without Neurological Complications
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    Chapter 5 Expression and Purification of E2 Glycoprotein from Insect Cells (Sf9) for Use in Serology
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    Chapter 6 Diagnostic Methods for CHIKV Based on Serological Tools
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    Chapter 7 Utilization and Assessment of Throat Swab and Urine Specimens for Diagnosis of Chikungunya Virus Infection
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    Chapter 8 Propagation of Chikungunya Virus Using Mosquito Cells
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    Chapter 9 Infectious Viral Quantification of Chikungunya Virus—Virus Plaque Assay
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    Chapter 10 Detection and Quantification of Chikungunya Virus by Real-Time RT-PCR Assay
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    Chapter 11 Chikungunya Virus
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    Chapter 12 Chikungunya Virus
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    Chapter 13 Chikungunya Virus Growth and Fluorescent Labeling: Detection of Chikungunya Virus by Immunofluorescence Assay
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    Chapter 14 Virus Isolation and Preparation of Sucrose-Banded Chikungunya Virus Samples for Transmission Electron Microscopy
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    Chapter 15 Chikungunya Virus
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    Chapter 16 Application of GelC-MS/MS to Proteomic Profiling of Chikungunya Virus Infection: Preparation of Peptides for Analysis
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    Chapter 17 Bioinformatics Based Approaches to Study Virus–Host Interactions During Chikungunya Virus Infection
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    Chapter 18 T-Cell Epitope Prediction of Chikungunya Virus
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    Chapter 19 Mouse Models of Chikungunya Virus
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    Chapter 20 Generation of Mouse Monoclonal Antibodies Specific to Chikungunya Virus Using ClonaCell-HY Hybridoma Cloning Kit
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    Chapter 21 Immunohistochemical Detection of Chikungunya Virus Antigens in Formalin-Fixed and Paraffin-Embedded Tissues
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    Chapter 22 Antiviral Strategies Against Chikungunya Virus
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    Chapter 23 A Real-Time Cell Analyzing Assay for Identification of Novel Antiviral Compounds against Chikungunya Virus
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    Chapter 24 Using Bicistronic Baculovirus Expression Vector System to Screen the Compounds That Interfere with the Infection of Chikungunya Virus
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    Chapter 25 Neutralization Assay for Chikungunya Virus Infection: Plaque Reduction Neutralization Test
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    Chapter 26 Reverse Genetics Approaches for Chikungunya Virus
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    Chapter 27 Chikungunya Virus
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    Chapter 28 Chikungunya Virus
Attention for Chapter 6: Diagnostic Methods for CHIKV Based on Serological Tools
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Chapter title
Diagnostic Methods for CHIKV Based on Serological Tools
Chapter number 6
Book title
Chikungunya Virus
Published in
Methods in molecular biology, May 2016
DOI 10.1007/978-1-4939-3618-2_6
Pubmed ID
Book ISBNs
978-1-4939-3616-8, 978-1-4939-3618-2
Authors

Paolo Gaibani, Maria Poala Landini, Vittorio Sambri

Editors

Justin Jang Hann Chu, Swee Kim Ang

Abstract

This chapter presents the most commonly used serological methods for the diagnosis of Chikungunya virus (CHIKV) infection in humans. CHIKV is a mosquito-borne Alphavirus widely distributed in the tropical and subtropical regions of Africa, Asia, and America. CHIKV infection in human causes acute febrile illness frequently accompanied by severe joint pain. Most of the infected patients may develop chronic arthralgia that may persist for several months or years. Laboratory diagnosis of CHIKV infection is mainly based on molecular and serological tests. The serological tests represent a valuable tool for diagnosis and epidemiological studies. Enzyme-linked immunosorbent assay (ELISA) and immunofluorescence assay (IFA) are simple, rapid, and sensitive techniques widely used for the diagnosis of CHIKV infection. However, these methods represent a screening tool and often require confirmation by a second-line assays. Serum virus neutralization assay is more specific than ELISA and IFA tests and is considered a confirmatory test. Neutralization assay is employed to determine the titer of virus neutralizing antibodies against CHIKV in patients' sera. The basis of microneutralization assay (MNA), results interpretation, and procedures will be illustrated in this chapter.

Mendeley readers

Mendeley readers

The data shown below were compiled from readership statistics for 46 Mendeley readers of this research output. Click here to see the associated Mendeley record.

Geographical breakdown

Country Count As %
United States 1 2%
Germany 1 2%
Saint Kitts and Nevis 1 2%
Unknown 43 93%

Demographic breakdown

Readers by professional status Count As %
Researcher 6 13%
Other 5 11%
Student > Ph. D. Student 4 9%
Student > Master 4 9%
Student > Bachelor 3 7%
Other 8 17%
Unknown 16 35%
Readers by discipline Count As %
Medicine and Dentistry 8 17%
Biochemistry, Genetics and Molecular Biology 7 15%
Agricultural and Biological Sciences 3 7%
Immunology and Microbiology 3 7%
Nursing and Health Professions 1 2%
Other 5 11%
Unknown 19 41%