Abstract
Chikungunya virus (CHIKV) is known to cause sporadic or explosive outbreaks. However, little is known about the endemic transmission of CHIKV. To ascertain the endemic occurrence of CHIKV transmission, we tested blood samples from patients with a non-dengue febrile illness who participated in a prospective cohort study of factory workers in Bandung, Indonesia. From August 2000 to June 2004, and September 2006 to April 2008, 1901 febrile episodes occurred and 231 (12.2%) dengue cases were identified. The remaining febrile cases were evaluated for possible CHIKV infection by measuring anti-CHIKV IgM and IgG antibodies in acute and convalescent samples. Acute samples of serologically positive cases were subsequently tested for the presence of CHIKV RNA by RT-PCR and/or virus isolation. A total of 135 (7.1%) CHIKV infections were identified, providing an incidence rate of 10.1/1,000 person years. CHIKV infections were identified all year round and tended to increase during the rainy season (January to March). Severe illness was not found and severe arthralgia was not a prominently reported symptom. Serial post-illness samples from nine cases were tested to obtain a kinetic picture of IgM and IgG anti-CHIKV antibodies. Anti-CHIKV IgM antibodies were persistently detected in high titers for approximately one year. Three patients demonstrated evidence of possible sequential CHIKV infections. The high incidence rate and continuous chikungunya cases in this adult cohort suggests that CHIKV is endemically transmitted in Bandung. Further characterization of the circulating strains and surveillance in larger areas are needed to better understand CHIKV epidemiology in Indonesia.
Publication types
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Research Support, Non-U.S. Gov't
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Research Support, U.S. Gov't, Non-P.H.S.
MeSH terms
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Adolescent
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Adult
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Aged
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Alphavirus Infections / epidemiology*
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Alphavirus Infections / virology
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Antibodies, Viral / blood
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Chikungunya virus / genetics
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Chikungunya virus / isolation & purification*
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Cohort Studies
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Endemic Diseases*
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Female
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Humans
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Immunoglobulin G / blood
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Immunoglobulin M / blood
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Incidence
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Indonesia / epidemiology
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Male
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Middle Aged
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Molecular Sequence Data
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Prospective Studies
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RNA, Viral / genetics
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Reverse Transcriptase Polymerase Chain Reaction
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Sequence Analysis, DNA
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Young Adult
Substances
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Antibodies, Viral
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Immunoglobulin G
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Immunoglobulin M
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RNA, Viral
Associated data
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GENBANK/KC879559
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GENBANK/KC879560
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GENBANK/KC879561
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GENBANK/KC879562
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GENBANK/KC879563
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GENBANK/KC879564
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GENBANK/KC879565
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GENBANK/KC879566
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GENBANK/KC879567
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GENBANK/KC879568
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GENBANK/KC879569
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GENBANK/KC879570
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GENBANK/KC879571
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GENBANK/KC879572
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GENBANK/KC879573
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GENBANK/KC879574
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GENBANK/KC879575
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GENBANK/KC879576
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GENBANK/KC879577
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GENBANK/KC879578
Grants and funding
This work was supported by the Military Infectious Diseases Research Program, Work Unit Number: 6000 RAD1.S.B0302 and the Department of State Biosecurity Engagement Program. QdM is supported by the Noaber foundation and Augeo foundation. The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript. The views expressed in this article are those of the authors and do not necessarily reflect the official policy or position of the Department of the Navy, Department of Defense, nor the U.S. Government. Some of the authors are military service members or employees of the U.S. Government. This work was prepared as part of their official duties. Title 17 U.S.C. §105 provides that ‘Copyright protection under this title is not available for any work of the United States Government.’ Title 17 U.S.C. §101 defines a U.S. Government work as a work prepared by a military service member or employee of the U.S. Government as part of that person's official duties.