Skip directly to local search Skip directly to A to Z list Skip directly to navigation Skip directly to site content Skip directly to page options
CDC Home

Volume 15, Number 4—April 2009

Dispatch

Concurrent Chikungunya and Dengue Virus Infections during Simultaneous Outbreaks, Gabon, 2007

Eric M. LeroyComments to Author , Dieudoné Nkoghe, Benjamin Ollomo, Chimène Nze-Nkogue, Pierre Becquart, Gilda Grard, Xavier Pourrut, Rémi N. Charrel, Grégory Moureau, Angélique Ndjoyi-Mbiguino, and Xavier de Lamballerie
Author affiliations: Centre International de Recherches Médicales de Franceville, Franceville, Gabon (E.M. Leroy, D. Nkoghe, B. Ollomo, C. Nze-Nkogue, P. Becquart, G. Grard, X. Pourrut); Université de la Méditerranée, Marseille, France (R. Charrel, G. Moureau, X. De Lamballerie); Université des Sciences de la Santé, Libreville, Gabon (A. Ndjoyi-Mbiguino)

Suggested citation for this article

Abstract

An outbreak of febrile illness occurred in Gabon in 2007, with 20,000 suspected cases. Chikungunya or dengue-2 virus infections were identified in 321 patients; 8 patients had documented co-infections. Aedes albopictus was identified as the principal vector for the transmission of both viruses.

In the past 20 years, dengue virus (DENV) and chikungunya virus (CHIKV) have caused large and geographically wide ranging epidemics (1,2). Recent CHIKV outbreaks caused several million clinical cases in the Indian Ocean Islands and India (3). The virus has also dispersed to new regions, including Gabon in Africa and Italy (4,5). DENVs cause the most notable mosquito-borne viral disease in the world; ≈100 million infections occur annually worldwide, and the incidence has increased >30-fold in the past 50 years (1). Despite this tremendous expansion of both diseases, relatively few cases of Chikungunya fever have been reported in Africa (3,6,7), and few dengue-2 virus (DENV-2) epidemics have been reported (8,9). Simultaneous CHIKV and DENV-2 outbreaks have rarely been observed.

CHIKV and DENV-2 are frequently transmitted to humans by peridomestic Aedes mosquitoes. Ae. aegypti has been considered to be the principal vector in the urban transmission cycle, with Ae. albopictus and other anthropophilic Aedes spp. serving as secondary vectors (10,11). However, the actual situation is much more complex. First, Ae. albopictus was repeatedly shown to be a highly competent vector of CHIKV during the recent outbreaks in the Indian Ocean and Italy (5,12). Second, the overall distribution of Aedes mosquitoes is rapidly changing. Specifically, Ae. albopictus (the Asian tiger mosquito) has dispersed globally into new territories previously occupied by Ae. aegypti. As a consequence, the characteristics of DENV and CHIKV circulation and their outbreak dynamics are likely to be modified.

The Study

Figure 1

Thumbnail of Chikungunya and dengue outbreaks in Gabon, 2007. Distribution of the outbreak and location of the 7 towns where suspected cases have been laboratory confirmed by using quantitative reverse transcription–PCR assay are shown. Chikungunya cases are represented by red circles, dengue cases by blue circles, and cases negative for the viruses by green circles. Testing methods are described in the footnote to the Table.

Figure 1. Chikungunya and dengue outbreaks in Gabon, 2007. Distribution of the outbreak and location of the 7 towns where suspected cases have been laboratory confirmed by using quantitative reverse transcription–PCR assay are...

We report an arboviral outbreak that occurred in Gabon, Central Africa, from March through July 2007, which showed the unexpected extent of the spread of Ae. albopictus populations in peridomestic urban areas. We also describe its association with atypical epidemiologic characteristics such as the co-circulation of CHIKV and DENV-2 and the frequency of human co-infections. The outbreak centered on the capital of Gabon; peaked from April through May 2007, in the heat of the long wet season; and subsequently moved north, where the virus sequentially reached several small towns along the route to northern Gabon and Cameroon (Figure 1). The outbreak generated ≈20,000 cases. Patients with suspected cases exhibited a dengue-like syndrome, including fever, arthralgia, and asthenia. Conjunctival hemorrhage, maculopapular rash, headache, and vomiting were also observed in the most severe cases.

During the course of the outbreak, 773 early blood samples (i.e., obtained during the first week after the onset of the disease) were collected from febrile patients who visited identified medical health centers in Libreville and other towns in Gabon (Table). Samples were tested for the presence of various arboviral RNA genomes by using the TaqMan quantitative reverse transcription–PCR (qRT-PCR) technology and specific primers and probes (protocols available upon request to the corresponding author). Among these 773 patients, 275 and 54 were positive for CHIKV and DENV, respectively, during May and July 2007 (Table), with 8 cases of co-infections. Using a dengue serotype-specific qRT-PCR assay, we showed that all DENV patients were positive for serotype 2 (DENV-2). In all 7 towns investigated on the route from Libreville to Cameroon (530 km), both CHIKV and DENV-2 human cases were reported, except in Cocobeach where only laboratory DENV-2 confirmed cases were observed (Figure 1).

To investigate this atypical scenario further, we analyzed 4,807 mosquitoes belonging to various species of Aedes (2,504 Ae. albopictus, 1,035 Ae. aegypti, 57 Aedes sympsoni), Culex (843 Cx. quinquefasciatus, 47 Cx. sp.), Anopheles (78 An. gambiae) and Mansonia (120 M. africana, 123 M. uniformis) in 15 different locations in Libreville where CHIKV or DENV-2 laboratory confirmed human cases were detected. Pools of 20 mosquitoes (constituted according to species and place of collection) were homogenized by using GenoGrinder 2000 (OPS Diagnostics, Bridgewater, NJ, USA) technology, and then tested for CHIKV and DENV-2 by qRT-PCR. We found that 7 and 3 groups of Ae. albopictus were positive for CHIKV and DENV-2, respectively, while no group containing other mosquito species was positive, indicating that Ae. albopictus was the only or at least the prominent vector of the 2 viruses.

Figure 2

Thumbnail of Phylogenetic relationships among dengue-2 virus (DENV-2) isolates based on full-length sequences (10,695 nt). A total of 85 DENV-2 genomes were compared with the human isolate obtained during the Gabon outbreak. Phylogeny was inferred by using neighbor-joining analysis. A neighbor-joining tree was constructed by using MEGA version 3.2 (www.megasoftware.net) with the Kimura 2-parameter corrections of multiple substitutions. Reliability of nodes was assessed by bootstrap resampling wi

Figure 2. Phylogenetic relationships among dengue-2 virus (DENV-2) isolates based on full-length sequences (10,695 nt). A total of 85 DENV-2 genomes were compared with the human isolate obtained during the Gabon outbreak. Phylogeny...

These data provide evidence for the presence of CHIKV and DENV in Gabon and for their transmission to humans by Ae. albopictus. These epidemiologic results also confirm our previous observation that CHIKV strains isolated during the Gabon outbreak in 2007 belong to the Central African lineage and harbor the A226V mutation as a result of adaptation to Ae. albopictus through a mechanism of evolutionary convergence (4). More surprisingly, our results show that the spread of this mosquito in an area previously occupied predominantly by Ae. aegypti (13) was accompanied by the simultaneous emergence and transmission of DENV-2. One DENV-2 strain (designated as Libreville 2007), isolated from 1 febrile patient by using E6 Vero cells was further characterized by full-length genome sequencing (10,695 nt). Phylogenetic analysis showed that the DENV-2 Gabon 2007 strain belongs to the cosmopolitan, rather than the sylvatic, genotype (Figure 2). This cosmopolitan genotype includes mainly Asian but also related strains isolated in India, Australia, Mexico, the Indian Ocean, and Africa (Uganda, Somalia, and Burkina Faso), presumably the result of travel to these remote locations by viremic patients or the transportation of commercial goods by ship.

Conclusions

Taken together, these findings document CHIKV and DENV-2 co-circulation that resulted in large simultaneous outbreaks in regions where Ae. albopictus was shown to be the principal vector. Notably, we identified 8 patients with blood samples that tested positive for the presence of both CHIKV and DENV-2 genomes, indicating co-infection of these patients by both viruses. However, while unlikely, genetic exchanges between the 2 viruses, either by recombination or complementation, are not definitively excluded. Clinical examination of these patients (all adults, 5 women and 3 men) did not identify specific or severe symptoms, although given the limited number of cases and clinical and biologic investigations, this observation should be interpreted with caution.

Although the DENV cases were few, 8 of 48 (≈17%) DENV-2 positive patients from towns affected by the 2 outbreaks tested positive for CHIKV (Table). Extrapolation of this result suggests that the total number of DENV-2 patients who are superinfected with CHIKV is likely to be high, which suggests that DENV-2 infection is not the antagonist for a secondary CHIKV infection. In contrast, only ≈3% of CHIKV+ patients were also DENV-2+; however, the starting period of time of infection or the sequence of infection by the 2 viruses cannot be assessed.

Although concurrent infections of dengue and chikungunya have been reported (14), such DENV-2 and CHIKV co-infections have never been previously associated with transmission by Ae. albopictus. Our study therefore provides a disconcerting example of the unexpected epidemiologic patterns that may be associated with the dispersal of both vectors (Ae. albopictus and Ae. aegypti) and pathogenic arboviruses (such as DENV and CHIKV). Ae. albopictus mosquitoes are now present in several temperate countries of the Northern Hemisphere where, given the opportunity, they could cause future arboviral epidemics. The recent sustained indigenous transmission of CHIKV by Ae. albopictus in northern Italy (5) provides a potential warning of what might occur much more frequently in the future in Europe and even in North America. Introduction of DENV or CHIKV in these regions are likely to generate indigenous transmission by Ae. albopictus.

Dr Leroy is the head of the emergent viral diseases unit at the Centre International Médicales de Franceville, Franceville, Gabon. He is also a senior scientist at the UMR190 of the Institut de Recherche pour le Développement, Marseille, France. His research interests focus on emergent viruses in Africa, especially highly lethal pathogens such as filoviruses and arboviruses.

Acknowledgments

We thank L. Ninove and K. Barthelemy for sequencing the DENV-2 genome. We also thank C. Paupy, E. Nchoutpouen, and B. Kamgang for help in mosquito characterization and E. Gould for assistance in preparing the manuscript.

Centre International de Recherches Médicales de Franceville is supported by the Government of Gabon, Total-Fina-Elf Gabon, and the Ministère de la Coopération Française. This work was also supported by a grant from the Institut de Recherche pour le Développement.

References

  1. Gubler DJ. Epidemic dengue/dengue hemorrhagic fever as a public health, social and economic problem in the 21st century. Trends Microbiol. 2002;10:1003. DOIPubMed
  2. Charrel RN, de Lamballerie X, Raoult D. Chikungunya outbreaks—the globalization of vectorborne diseases. N Engl J Med. 2007;356:76971. DOIPubMed
  3. Pialoux G, Gauzere BA, Jaureguiberry S, Strobel M. Chikungunya, an epidemic arbovirosis. Lancet Infect Dis. 2007;7:31927. DOIPubMed
  4. de Lamballerie X, Leroy E, Charrel RN, Ttsetsarkin K, Higgs S, Gould EA. Chikungunya virus adapts to tiger mosquito via evolutionary convergence: a sign of things to come? Virol J. 2008;5:33. DOIPubMed
  5. Rezza G, Nicoletti L, Angelini R, Romi R, Finarelli AC, Panning M, Infection with chikungunya virus in Italy: an outbreak in a temperate region. Lancet. 2007;370:18406. DOIPubMed
  6. Pastorino B, Muyembe-Tamfum JJ, Bessaud M, Tock F, Tolou H, Durand JP, Epidemic resurgence of chikungunya virus in democratic Republic of the Congo: identification of a new central African strain. J Med Virol. 2004;74:27782. DOIPubMed
  7. Peyrefitte CN, Rousset D, Pastorino BA, Pouillot R, Bessaud M, Tock F, Chikungunya virus, Cameroon, 2006. Emerg Infect Dis. 2007;13:76871.PubMed
  8. Thomas SJ, Strickman D, Vaughn DW. Dengue epidemiology: virus epidemiology, ecology, and emergence. Adv Virus Res. 2003;61:23589. DOIPubMed
  9. Vasilakis N, Tesh RB, Weaver SC. Sylvatic dengue virus type 2 activity in humans, Nigeria, 1966. Emerg Infect Dis. 2008;14:5024. DOIPubMed
  10. Moncayo AC, Fernandez Z, Ortiz D, Diallo M, Sall A, Hartman S, Dengue emergence and adaptation to peridomestic mosquitoes. Emerg Infect Dis. 2004;10:17906.PubMed
  11. Gratz NG. Critical review of the vector status of Aedes albopictus. Med Vet Entomol. 2004;18:21527. DOIPubMed
  12. Tsetsarkin KA, Vanlandingham DL, McGee CE, Higgs S. A single mutation in chikungunya virus affects vector specificity and epidemic potential. PLoS Pathog. 2007;3:e201. DOIPubMed
  13. Twiddy SS, Farrar JJ, Vinh Chau N, Wills B, Gould EA, Gritsun T, Phylogenetic relationships and differential selection pressures among genotypes of dengue-2 virus. Virology. 2002;298:6372. DOIPubMed
  14. Myers RM, Carey DE. Concurrent isolation from patient of two arboviruses, chikungunya and dengue type 2. Science. 1967;157:13078. DOIPubMed

Figures

Table

Suggested citation for this article: Leroy EM, Nkoghe D, Ollomo B, Nze-Nkogue C, Becquart P, Grard G, Pourrut X, et al. Concurrent chikungunya and dengue virus infections during simultaneous outbreaks, Gabon, 2007. Emerg Infect Dis [serial on the Internet]. 2009 Apr [date cited]. Available from http://wwwnc.cdc.gov/eid/article/15/4/08-0664.htm

DOI: 10.3201/eid1504.080664

Top of Page

Table of Contents – Volume 15, Number 4—April 2009

Comments to the Authors

Please use the form below to submit correspondence to the authors or contact them at the following address:

Eric M. Leroy, UMR190 IRD/CIRMF, BP 769 Franceville, Gabon





characters(s) remaining.

Comment submitted successfully, thank you for your feedback.

Comments to the EID Editors

Please contact the EID Editors via our Contact Form.

 

Past Issues

Select a Past Issue:

World Malaria Day - April 25, 2014 - Invest in the future, defeat malaria

20th Anniversary - National Infant Immunization Week - Immunization. Power to Protect.

Art in Science - Selections from Emerging Infectious Diseases
Now available for order



CDC 24/7 – Saving Lives, Protecting People, Saving Money. Learn More About How CDC Works For You…

USA.gov: The U.S. Government's Official Web PortalDepartment of Health and Human Services
Centers for Disease Control and Prevention   1600 Clifton Rd. Atlanta, GA 30333, USA
800-CDC-INFO (800-232-4636) TTY: (888) 232-6348 - Contact CDC–INFO