In 2025, global public health faces renewed challenges as Chikungunya virus (CHIKV) emerges as a critical focus due to its rapid spread and debilitating joint pain. The World Health Organization (WHO) has sounded the alarm on the risk of a global CHIKV epidemic, citing its potential to overwhelm healthcare systems in tropical and subtropical regions. In Foshan’s Shunde District, an outbreak sparked by an imported case on July 8 led to 478 confirmed cases within a week, primarily in Lecong, Beijiao, and Chencun, underscoring the urgency of mosquito-borne transmission control. abinScience is committed to advancing CHIKV research by providing high-quality tools to study its structure, pathogenesis, and vaccine development, empowering researchers worldwide to combat this growing threat.
As of 5:03 PM on July 16, 2025, the Foshan outbreak remains dynamic, with most cases presenting mild symptoms but rapid case growth raising concerns. Globally, CHIKV affects approximately 16.9 million people annually across 111 countries, driven by Aedes aegypti and Aedes albopictus mosquitoes. Climate change and urbanization exacerbate its spread. The virus’s name, derived from the Kimakonde word meaning “to become contorted,” reflects the severe joint pain that leaves patients physically incapacitated, highlighting its escalating threat to global health.
Fig. 1. Current transmission dynamics of alphaviruses (de Souza WM, Lecuit M, Weaver SC).
Virus Structure and Pathogenesis
Chikungunya virus (CHIKV), a member of the Togaviridae family and Alphavirus genus, possesses a single-stranded positive-sense RNA genome of approximately 11.8 kb. It encodes four nonstructural proteins (nsP1–nsP4) and five structural proteins (C, E3, E2, 6K, E1). The virus particle, nearly spherical and 60–70 nm in diameter, comprises a lipid envelope, capsid, and genomic RNA, with a modular, symmetrical structure optimized for efficient transmission. CHIKV enters cells via E1-E2 heterodimer-mediated membrane fusion, replicating in skin and fibroblast cells before disseminating to multiple organs. This triggers acute symptoms like fever and joint pain. Viral replication induces inflammation and tissue damage, leading to chronic sequelae such as persistent arthralgia (lasting months to years), rare central nervous system infections, and potential pregnancy complications. Impacts on bone health remain under investigation.
Fig. 2. Chikungunya virus involves a 12 kb RNA genome encoding four nonstructural and five structural proteins (doi.org/10.1016/j.rmu.2017.09.001).
Overview of CHIKV Pathogenic Proteins
CHIKV’s pathogenicity hinges on its encoded proteins, which drive critical stages of the viral life cycle, including replication, assembly, and immune evasion. The table below details the functions and characteristics of the four nonstructural (nsP1–nsP4) and five structural proteins (C, E3, E2, 6K, E1), alongside their potential in research and therapeutic applications, offering key insights for vaccine and antiviral development.
Protein Name | Function and Characteristics | Research and Applications |
---|---|---|
nsP1 Protein | Exhibits methyltransferase and helicase activity, critical for early viral replication. Adds a 5' cap to viral RNA, ensuring stability and recognition by host ribosomes, and anchors the replication complex to membranes. | - |
nsP2 Protein | Multifunctional protein with helicase and protease activity. Cleaves viral polyprotein precursors to produce functional nsP1–nsP4 and suppresses host interferon responses, aiding immune evasion. | Neutralizing antibodies targeting nsP2 show preliminary therapeutic potential. |
nsP3 Protein | Facilitates replication complex assembly and stabilization, enhancing replication efficiency. Interacts with host proteins to regulate RNA synthesis and may influence viral cellular localization. | nsP3 hypervariable region used in Ixchiq vaccine attenuation design. |
nsP4 Protein | RNA-dependent RNA polymerase (RdRp), the core replication enzyme, synthesizing genomic and subgenomic RNA, critical for the viral life cycle. | Common target for antiviral drug development. |
C Protein (Capsid) | Located inside the virion, recognizes and packages RNA to form the nucleocapsid. Interacts with E2 to link the capsid to the envelope, facilitating particle assembly. | - |
E3 Protein | Co-translated with E2, assists in E2 folding and stabilization. Typically cleaved during budding, but residual E3 may influence immunogenicity or stability. | - |
E2 Protein | Recognizes and binds host receptors, initiating attachment. Major surface antigen, eliciting robust immune responses. | Core target for vaccines and neutralizing antibodies; Ixchiq and Vimkunya target E2, offering immunity for at least two years. |
E1 Protein | Fusion protein, undergoing conformational changes in acidic environments to mediate envelope-cell membrane fusion, enabling RNA entry. | Used with E2 in Vimkunya’s virus-like particle design. |
6K Protein | Auxiliary structural protein, aiding budding and envelope formation, ensuring proper E1/E2 localization. | - |
Vaccine Development and Research Progress
CHIKV vaccine development has achieved significant milestones, with two vaccines currently approved: Ixchiq (FDA-approved), a live-attenuated vaccine based on a CHIKV strain with a deleted nsP3 hypervariable region to reduce virulence, and Vimkunya, a virus-like particle (VLP) vaccine leveraging E1/E2 protein expression to induce robust immunity. Neutralizing antibodies, such as CHK-152, demonstrate cross-protection across CHIKV lineages, broadening vaccine and therapeutic potential. While no specific antiviral drugs are widely available, relying on symptomatic treatment, advances in antibodies, siRNA, and inhibitors targeting E2 and nsP2 offer promise. Ixchiq provides hope for prevention, but challenges remain in scaling supply chains and verifying long-term efficacy, particularly in light of WHO’s warnings about epidemic risks.
Fig. 3. Overview of CHIKV vaccine types (de Souza WM, Lecuit M, Weaver SC).
About abinScience
Founded in France in 2023, abinScience specializes in developing and producing high-quality research reagents. We provide innovative, reliable tools for global researchers, leveraging advanced technology platforms and stringent quality control. Our product portfolio spans autoimmunity, bacterial/viral infections, neuroscience, and immune targets, including antibodies, recombinant proteins, detection kits, and functional tools, renowned for high sensitivity and specificity in supporting basic and translational research.
abinScience CHIKV-Related Products
Below is a list of abinScience’s CHIKV-related protein and antibody products. For more details, scan the QR code to connect with our dedicated advisors!
Type | Catalog Number | Product Name |
---|---|---|
Protein | VK572011 | Recombinant CHIKV Spike glycoprotein E2 Protein, C-Fc |
VK572021 | Recombinant CHIKV Spike glycoprotein E2 Protein, C-His | |
VK640012 | Recombinant CHIKV NSP2 Protein, N-GST-His | |
VK425011 | Recombinant CHIKV Spike glycoprotein E1 Protein, C-Fc | |
VK425012 | Recombinant CHIKV Spike glycoprotein E1 Protein, N-His | |
VK572012 | Recombinant CHIKV Spike glycoprotein E2, N-His | |
VK572022 | Recombinant CHIKV Capsid Protein, N-His | |
VK640022 | Recombinant CHIKV NSP1 Protein, N-His | |
VK640032 | Recombinant CHIKV NSP3 Protein, N-His | |
Antibody | VK425010 | InVivoMAb Anti-Chikungunya Virus/CHIKV VLP Antibody (m242) |
VK572013 | Anti-CHIKV Spike glycoprotein E2 Antibody (CHK265) | |
VK572023 | Anti-CHIKV Spike glycoprotein E2 Antibody (5M16) | |
VK572033 | Anti-CHIKV Spike glycoprotein E2 Antibody (4J21) | |
VK572043 | Anti-CHIKV Spike glycoprotein E2 Antibody (5F10) | |
VK425013 | Anti-CHIKV p130/Structural polyprotein Antibody (9.8B) | |
VK425023 | Anti-CHIKV p130/Structural polyprotein Antibody (CHK152) | |
VK425033 | Anti-CHIKV p130/Structural polyprotein Antibody (DC1.370) | |
VK425043 | Anti-CHIKV p130/Structural polyprotein Antibody (DC1.380) | |
VK425053 | Anti-CHIKV p130/Structural polyprotein Antibody (DC1.415) | |
VK425063 | Anti-CHIKV p130/Structural polyprotein Antibody (DC1.55) | |
VK425073 | Anti-CHIKV p130/Structural polyprotein Antibody (DC1.56) | |
VK425083 | Anti-CHIKV p130/Structural polyprotein Antibody (DC1.7) | |
VK425093 | Anti-CHIKV p130/Structural polyprotein Antibody (DC1.9) | |
VK425103 | Anti-CHIKV p130/Structural polyprotein Antibody (DC2.550B) | |
VK425113 | Anti-CHIKV p130/Structural polyprotein Antibody (DC2.74) | |
VK425123 | Anti-CHIKV p130/Structural polyprotein Antibody (DC2.82) | |
VK425133 | Anti-CHIKV p130/Structural polyprotein Antibody (DC2.85) | |
VK425143 | Anti-CHIKV p130/Structural polyprotein Antibody (DC2.112) | |
VK425153 | Anti-CHIKV p130/Structural polyprotein Antibody (DC2.315) | |
VK425014 | Anti-CHIKV Spike glycoprotein E1 Polyclonal Antibody | |
VK640014 | Anti-CHIKV NSP2 Protein Polyclonal Antibody | |
VK572014 | Anti-CHIKV Spike glycoprotein E2 Polyclonal Antibody | |
VK572024 | Anti-CHIKV Capsid Protein Polyclonal Antibody | |
VK640024 | Anti-CHIKV NSP1 Polyclonal Antibody | |
VK640034 | Anti-CHIKV NSP3 Polyclonal Antibody |
For more product information, contact: info@abinscience.com
References
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