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Published in: Malaria Journal 1/2016

Open Access 01-12-2016 | Research

Concurrent malaria and arbovirus infections in Kedougou, southeastern Senegal

Authors: Abdourahmane Sow, Cheikh Loucoubar, Diawo Diallo, Oumar Faye, Youssoupha Ndiaye, Cheikh Saadibou Senghor, Anta Tal Dia, Ousmane Faye, Scott C. Weaver, Mawlouth Diallo, Denis Malvy, Amadou Alpha Sall

Published in: Malaria Journal | Issue 1/2016

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Abstract

Background

Malaria is one of the leading causes of acute febrile illness (AFI) in Africa. With the advent of malaria rapid diagnostic tests, misdiagnosis and co-morbidity with other diseases has been highlighted by an increasing number of studies. Although arboviral infections and malaria are both vector-borne diseases and often have an overlapping geographic distribution in sub-Saharan Africa, information about their incidence rates and concurrent infections is scarce.

Methods

From July 2009 to March 2013 patients from seven healthcare facilities of the Kedougou region presenting with AFI were enrolled and tested for malaria and arboviral infections, i.e., yellow fever (YFV), West Nile (WNV), dengue (DENV), chikungunya (CHIKV), Crimean Congo haemorrhagic fever (CCHFV), Zika (ZIKV), and Rift Valley fever viruses (RVFV). Malaria parasite infections were investigated using thick blood smear (TBS) and rapid diagnostics tests (RDT) while arbovirus infections were tested by IgM antibody detection (ELISA) and RT-PCR assays. Data analysis of single or concurrent malaria and arbovirus was performed using R software.

Results

A total of 13,845 patients, including 7387 with malaria and 41 with acute arbovirus infections (12 YFV, nine ZIKV, 16 CHIKV, three DENV, and one RVFV) were enrolled. Among the arbovirus-infected patients, 48.7 % (20/41) were co-infected with malaria parasites at the following frequencies: CHIKV 18.7 % (3/16), YFV 58.3 % (7/12), ZIKV 88.9 % (8/9), DENV 33.3 % (1/3), and RVF 100 % (1/1). Fever ≥40 °C was the only sign or symptom significantly associated with dual malaria parasite/arbovirus infection.

Conclusions

Concurrent malaria parasite and arbovirus infections were detected in the Kedougou region from 2009 to 2013 and need to be further documented, including among asymptomatic individuals, to assess its epidemiological and clinical impact.
Literature
1.
go back to reference Mohapatra MK, Patra P, Agrawala R. Manifestation and outcome of concurrent malaria and dengue infection. J Vector Borne Dis. 2012;49:262–5.PubMed Mohapatra MK, Patra P, Agrawala R. Manifestation and outcome of concurrent malaria and dengue infection. J Vector Borne Dis. 2012;49:262–5.PubMed
2.
go back to reference Mushtaq MB, Qadri MI, Rashid A. Concurrent infection with dengue and malaria: an unusual presentation. Case Rep Med. 2013;2013:520181.PubMedPubMedCentral Mushtaq MB, Qadri MI, Rashid A. Concurrent infection with dengue and malaria: an unusual presentation. Case Rep Med. 2013;2013:520181.PubMedPubMedCentral
3.
go back to reference Carme B, Matheus S, Donutil G, Raulin O, Nacher M, Morvan J. Concurrent dengue and malaria in Cayenne Hospital, French Guiana. Emerg Infect Dis. 2009;15:668–71.PubMedPubMedCentralCrossRef Carme B, Matheus S, Donutil G, Raulin O, Nacher M, Morvan J. Concurrent dengue and malaria in Cayenne Hospital, French Guiana. Emerg Infect Dis. 2009;15:668–71.PubMedPubMedCentralCrossRef
4.
go back to reference Arya CS, Mehta KL, Agarwal N, Agarwal BK, Mathai G, Moondhara A. Episodes of concurrent dengue and malaria. Dengue Bull. 2005;29:208–9. Arya CS, Mehta KL, Agarwal N, Agarwal BK, Mathai G, Moondhara A. Episodes of concurrent dengue and malaria. Dengue Bull. 2005;29:208–9.
5.
go back to reference Deresinski S. Concurrent Plasmodium vivax malaria and dengue. Emerg Infect Dis. 1802;2006:12. Deresinski S. Concurrent Plasmodium vivax malaria and dengue. Emerg Infect Dis. 1802;2006:12.
6.
go back to reference Abbasi A, Butt N, Sheikh QH, Bhutto AR, Munir SM, Ahmed SM. Clinical features, diagnostic techniques and management of dual dengue and malaria infection. J Coll Physicians Surg Pak. 2009;19:25–9.PubMed Abbasi A, Butt N, Sheikh QH, Bhutto AR, Munir SM, Ahmed SM. Clinical features, diagnostic techniques and management of dual dengue and malaria infection. J Coll Physicians Surg Pak. 2009;19:25–9.PubMed
7.
go back to reference Ali N, Nadeem A, Anwar M, Tariq WU, Chotani RA. Dengue fever in malaria endemic areas. J Coll Physicians Surg Pak. 2006;16:340–2.PubMed Ali N, Nadeem A, Anwar M, Tariq WU, Chotani RA. Dengue fever in malaria endemic areas. J Coll Physicians Surg Pak. 2006;16:340–2.PubMed
8.
go back to reference Ward DI. A case of fatal Plasmodium falciparum malaria complicated by acute dengue fever in East Timor. Am J Trop Med Hyg. 2006;75:182–5.PubMed Ward DI. A case of fatal Plasmodium falciparum malaria complicated by acute dengue fever in East Timor. Am J Trop Med Hyg. 2006;75:182–5.PubMed
9.
go back to reference Thangaratham PS, Jeevan MK, Rajendran R, Samuel PP, Tyagi BK. Dual infection by dengue virus and Plasmodium vivax in Alappuzha District, Kerala, India. Jpn J Infect Dis. 2006;59:211–2.PubMed Thangaratham PS, Jeevan MK, Rajendran R, Samuel PP, Tyagi BK. Dual infection by dengue virus and Plasmodium vivax in Alappuzha District, Kerala, India. Jpn J Infect Dis. 2006;59:211–2.PubMed
10.
go back to reference Vdos Santana S, Lavezzo LC, Mondini A, Terzian AC, Bronzoni RV, Rossit AR, et al. Concurrent dengue and malaria in the Amazon region. Rev Soc Bras Med Trop. 2010;43:508–11.CrossRef Vdos Santana S, Lavezzo LC, Mondini A, Terzian AC, Bronzoni RV, Rossit AR, et al. Concurrent dengue and malaria in the Amazon region. Rev Soc Bras Med Trop. 2010;43:508–11.CrossRef
11.
go back to reference Senn N, Suarkia DL, Manong D, Siba PM, McBride WJH. Contribution of dengue fever to the burden of acute febrile illnesses in Papua New Guinea: an age-specific prospective study. Am J Trop Med Hyg. 2011;85:132–7.PubMedPubMedCentralCrossRef Senn N, Suarkia DL, Manong D, Siba PM, McBride WJH. Contribution of dengue fever to the burden of acute febrile illnesses in Papua New Guinea: an age-specific prospective study. Am J Trop Med Hyg. 2011;85:132–7.PubMedPubMedCentralCrossRef
12.
go back to reference Baba M, Logue CH, Oderinde B, Abdulmaleek H, Williams J, Lewis J, et al. Evidence of arbovirus co-infection in suspected febrile malaria and typhoid patients in Nigeria. J Infect Dev Ctries. 2013;7:51–9.PubMedCrossRef Baba M, Logue CH, Oderinde B, Abdulmaleek H, Williams J, Lewis J, et al. Evidence of arbovirus co-infection in suspected febrile malaria and typhoid patients in Nigeria. J Infect Dev Ctries. 2013;7:51–9.PubMedCrossRef
13.
go back to reference Monlun E, Zeller H, Le Guenno B, Traoré-Lamizana M, Hervy JP, Adam F, Ferrara L, Fontenille D, Sylla R, Mondo M, Digoutte JP. [Surveillance of the circulation of arbovirus of medical interest in the region of eastern Senegal (1988-1991)](in French). Bull Soc Pathol Exot. 1993;86:21–8.PubMed Monlun E, Zeller H, Le Guenno B, Traoré-Lamizana M, Hervy JP, Adam F, Ferrara L, Fontenille D, Sylla R, Mondo M, Digoutte JP. [Surveillance of the circulation of arbovirus of medical interest in the region of eastern Senegal (1988-1991)](in French). Bull Soc Pathol Exot. 1993;86:21–8.PubMed
14.
go back to reference WHO: Word malaria report 2010. Geneva: Word Health Organization. WHO: Word malaria report 2010. Geneva: Word Health Organization.
15.
go back to reference Robin Y, Cornet M, Heme G, Le Gonidec G. Isolement du virus de la dengue au Sénégal. Ann Virol (Inst. Pasteur). 1980;131E:149–54.CrossRef Robin Y, Cornet M, Heme G, Le Gonidec G. Isolement du virus de la dengue au Sénégal. Ann Virol (Inst. Pasteur). 1980;131E:149–54.CrossRef
17.
go back to reference Thiam S, Thior M, Faye B, Ndiop M, Diouf ML, Diouf MB, et al. Major reduction in antimalarial drug consumption in Senegal after nationwide introduction of malaria rapid diagnostic tests. PLoS One. 2011;6:e18419.PubMedPubMedCentralCrossRef Thiam S, Thior M, Faye B, Ndiop M, Diouf ML, Diouf MB, et al. Major reduction in antimalarial drug consumption in Senegal after nationwide introduction of malaria rapid diagnostic tests. PLoS One. 2011;6:e18419.PubMedPubMedCentralCrossRef
18.
go back to reference Programme national de lutte contre le paludisme au Sénégal. Rapport annuel. Dakar; 2009. Programme national de lutte contre le paludisme au Sénégal. Rapport annuel. Dakar; 2009.
19.
go back to reference Agence nationale de la démographie et de la Statistique (Service régional de Kédougou). Rapport annuel. Kedougou; 2012. Agence nationale de la démographie et de la Statistique (Service régional de Kédougou). Rapport annuel. Kedougou; 2012.
21.
go back to reference Organisation mondiale de la Santé: L’utilisation des tests diagnostiques rapides du paludisme. Genève: WHO publications; 2004. p. 19. Organisation mondiale de la Santé: L’utilisation des tests diagnostiques rapides du paludisme. Genève: WHO publications; 2004. p. 19.
22.
go back to reference WHO Guidelines for the treatment of malaria. Geneva: World Health Organization; 2010, p. 210. WHO Guidelines for the treatment of malaria. Geneva: World Health Organization; 2010, p. 210.
23.
24.
go back to reference Saluzzo JF, Anderson GW Jr, Hodgson LA, Digoutte JP, Smith JF. Antigenic and biological properties of Rift Valley fever virus isolated during the 1987 Mauritanian epidemic. Res Virol. 1989;140:155–64.PubMedCrossRef Saluzzo JF, Anderson GW Jr, Hodgson LA, Digoutte JP, Smith JF. Antigenic and biological properties of Rift Valley fever virus isolated during the 1987 Mauritanian epidemic. Res Virol. 1989;140:155–64.PubMedCrossRef
25.
go back to reference Weidmann M, Faye O, Faye O, Kranaster R, Marx A, Nunes MRT, et al. Improved LNA probe based assay for the detection of African and South-American Yellow Fever virus strains. J Clin Virol. 2010;48:187–92.PubMedCrossRef Weidmann M, Faye O, Faye O, Kranaster R, Marx A, Nunes MRT, et al. Improved LNA probe based assay for the detection of African and South-American Yellow Fever virus strains. J Clin Virol. 2010;48:187–92.PubMedCrossRef
26.
go back to reference Wu SJ, Pal S, Ekanayake S, Greenwald D, Lara S, Raviprakash K, et al. A dry-format field-deployable quantitative reverse transcriptase-polymerase chain reaction assay for diagnosis of dengue infections. Am J Trop Med Hyg. 2008;79:505–10.PubMed Wu SJ, Pal S, Ekanayake S, Greenwald D, Lara S, Raviprakash K, et al. A dry-format field-deployable quantitative reverse transcriptase-polymerase chain reaction assay for diagnosis of dengue infections. Am J Trop Med Hyg. 2008;79:505–10.PubMed
27.
go back to reference StataCorp. 2007. Stata Statistical Software: Release 10. College Station, TX: StataCorp LP. StataCorp. 2007. Stata Statistical Software: Release 10. College Station, TX: StataCorp LP.
28.
go back to reference R Development Core Team. R: a language and environment for statistical computing. R Foundation for Statistical Computing, Vienna: Austria 2008, ISBN 3-900051-07-0, URL. http://www.R-project.org. R Development Core Team. R: a language and environment for statistical computing. R Foundation for Statistical Computing, Vienna: Austria 2008, ISBN 3-900051-07-0, URL. http://​www.​R-project.​org.
29.
go back to reference Niang M, Thian LG, Sow A, Loucoubar C, Bob NS, Diop F, et al. A molecular Survey of acute febrile illnesses reveals Plasmodium vivax infections in Kedougou, southeastern Senegal. Malar J. 2015;14:281.PubMedPubMedCentralCrossRef Niang M, Thian LG, Sow A, Loucoubar C, Bob NS, Diop F, et al. A molecular Survey of acute febrile illnesses reveals Plasmodium vivax infections in Kedougou, southeastern Senegal. Malar J. 2015;14:281.PubMedPubMedCentralCrossRef
31.
go back to reference Traoré LM, Fontenille D, Zeller HG, Mondo M, Diallo M, Adam F, et al. Surveillance for yellow fever virus in eastern Senegal during 1993. J Med Entomol. 1996;33:760–5.CrossRef Traoré LM, Fontenille D, Zeller HG, Mondo M, Diallo M, Adam F, et al. Surveillance for yellow fever virus in eastern Senegal during 1993. J Med Entomol. 1996;33:760–5.CrossRef
32.
go back to reference Dia I, Diop T, Rakotoarivony I, Kengne P, Fontenille D. Bionomics of Anopheles gambiae Giles, An. arabiensis Patton, An. funestus Giles and An. nili (Theobald) (Diptera: Culicidae) and transmission of Plasmodium falciparum in a Sudano-Guinean zone (Ngari, Senegal). J Med Entomol. 2003;40:279–83.PubMedCrossRef Dia I, Diop T, Rakotoarivony I, Kengne P, Fontenille D. Bionomics of Anopheles gambiae Giles, An. arabiensis Patton, An. funestus Giles and An. nili (Theobald) (Diptera: Culicidae) and transmission of Plasmodium falciparum in a Sudano-Guinean zone (Ngari, Senegal). J Med Entomol. 2003;40:279–83.PubMedCrossRef
33.
go back to reference Diallo D, Sall AA, Buenemann M, Chen R, Faye O, Diagne CT, et al. Landscape ecology of sylvatic chikungunya virus and mosquito vectors in southeastern Senegal. PLoS Negl Trop Dis. 2012;6:e1649.PubMedPubMedCentralCrossRef Diallo D, Sall AA, Buenemann M, Chen R, Faye O, Diagne CT, et al. Landscape ecology of sylvatic chikungunya virus and mosquito vectors in southeastern Senegal. PLoS Negl Trop Dis. 2012;6:e1649.PubMedPubMedCentralCrossRef
34.
go back to reference Mwangugangi JM, Muturi EJ, Muriu SM, Nzovu J, Midega JT, Mbogo C. The role of Anopheles arabiensis and Anopheles coustani in indoor and outdoor malaria transmission in Taveta District, Kenya. Parasit Vectors. 2013;6:114.CrossRef Mwangugangi JM, Muturi EJ, Muriu SM, Nzovu J, Midega JT, Mbogo C. The role of Anopheles arabiensis and Anopheles coustani in indoor and outdoor malaria transmission in Taveta District, Kenya. Parasit Vectors. 2013;6:114.CrossRef
35.
go back to reference Le Port A, Cot M, Etard JF, Gaye O, Migot-Nabias F, Garcia A. Relation between Plasmodium falciparum asymptomatic infection and malaria attacks in a cohort of Senegalese children. Malar J. 2008;7:193.PubMedPubMedCentralCrossRef Le Port A, Cot M, Etard JF, Gaye O, Migot-Nabias F, Garcia A. Relation between Plasmodium falciparum asymptomatic infection and malaria attacks in a cohort of Senegalese children. Malar J. 2008;7:193.PubMedPubMedCentralCrossRef
36.
go back to reference Epelboin L, Hanf M, Dussart P, Ouar-Epelboin S, Djossou F, Nacher M, et al. Is dengue and malaria co-infection more severe than single infections? A retrospective matched-pair study in French Guiana. Malar J. 2012;11:142.PubMedPubMedCentralCrossRef Epelboin L, Hanf M, Dussart P, Ouar-Epelboin S, Djossou F, Nacher M, et al. Is dengue and malaria co-infection more severe than single infections? A retrospective matched-pair study in French Guiana. Malar J. 2012;11:142.PubMedPubMedCentralCrossRef
37.
go back to reference Mourembou G, Fenollar F, Socolovschi C, Lemamy GJ, Nzoughe H, Kouna LC, et al. Molecular detection of fastidious and common bacteria as well as Plasmodium spp. in febrile and afebrile children in Franceville, Gabon. Am J Trop Med Hyg. 2015;92:926–32. doi:10.4269/ajtmh.14-0699.PubMedCrossRef Mourembou G, Fenollar F, Socolovschi C, Lemamy GJ, Nzoughe H, Kouna LC, et al. Molecular detection of fastidious and common bacteria as well as Plasmodium spp. in febrile and afebrile children in Franceville, Gabon. Am J Trop Med Hyg. 2015;92:926–32. doi:10.​4269/​ajtmh.​14-0699.PubMedCrossRef
Metadata
Title
Concurrent malaria and arbovirus infections in Kedougou, southeastern Senegal
Authors
Abdourahmane Sow
Cheikh Loucoubar
Diawo Diallo
Oumar Faye
Youssoupha Ndiaye
Cheikh Saadibou Senghor
Anta Tal Dia
Ousmane Faye
Scott C. Weaver
Mawlouth Diallo
Denis Malvy
Amadou Alpha Sall
Publication date
01-12-2016
Publisher
BioMed Central
Published in
Malaria Journal / Issue 1/2016
Electronic ISSN: 1475-2875
DOI
https://doi.org/10.1186/s12936-016-1100-5

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