An urban epidemic of dengue in Senegal during 2009 affected 196 persons and included 5 cases of dengue hemorrhagic fever and 1 fatal case of dengue shock syndrome. Dengue virus serotype 3 was identified from all patients, and
Dengue is an arboviral disease transmitted by
Most dengue infections occur in urban areas in tropical and subtropical regions, but imported cases have been reported in nontropical regions. During October 2009, imported DENV-3 infections were diagnosed in Turin, Italy (
Geographic distribution of patients with confirmed dengue in the region of Dakar, Senegal. Number of patients is shown in parentheses. Inset shows location of Dakar in Senegal and in Africa.
During October 2009–January 2010, a total of 696 serum samples were collected from persons in Senegal who were suspected to have dengue. A suspected dengue case was defined as fever and
| Characteristic | Dakar | Thies | Louga | Other† | Total | ||||||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| Pateau | Almadies | Grand Dakar | Parcelle | Pikine | Guediawaye | Niayes | Thiaroye | Rufisque | |||||
| Suspected cases | 202 | 157 | 117 | 82 | 13 | 15 | 5 | 10 | 5 | 87 | 1‡ | 3 | 696 |
| Patient sex | |||||||||||||
| M | 91 | 60 | 56 | 44 | 8 | 10 | 2 | 6 | 2 | 38 | 1‡ | 3 | 320 |
| F | 111 | 97 | 61 | 38 | 5 | 5 | 3 | 4 | 3 | 49 | 0 | 0 | 376 |
| Patient age, y, median (range) | 30 (1–76) | 29 (2–79) | 38 (5–93) | 28 (3–60) | 25 (9–55) | 29 (20–35) | 33 (11–56) | 40 (8–78) | 45 (26–69) | 30 (6–69) | 32 | 53 | |
| Health facility visited | |||||||||||||
| Private laboratory | 144 | 125 | 64 | 40 | 2 | 0 | 5 | 0 | 5 | 0 | 1‡ | 0 | 385 |
| Private clinic | 23 | 10 | 0 | 0 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 34 |
| Public health | 35 | 22 | 53 | 42 | 10 | 15 | 0 | 10 | 0 | 87 | 0 | 3 | 277 |
| Patient nationality | |||||||||||||
| Senegalese | 96 | 98 | 89 | 82 | 13 | 15 | 5 | 10 | 5 | 87 | 1 | 3 | 504 |
| Lebanese | 86 | 11 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 98 |
| French | 13 | 33 | 6 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 52 |
| Lusophone | 5 | 14 | 20 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 39 |
| Chinese | 2 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 4 |
| Confirmed cases | 120 | 30 | 27 | 14 | 2 | 0 | 0 | 0 | 0 | 3 | 1‡ | 0 | 196 |
| Patient sex | |||||||||||||
| M | 56 | 12 | 12 | 8 | 0 | 0 | 0 | 0 | 0 | 1 | 1‡ | 0 | 89 |
| F | 64 | 18 | 15 | 6 | 2 | 0 | 0 | 0 | 0 | 2 | 0 | 0 | 107 |
| Patient age, y, median (range) | 32 (1–70) | 26 (6–42) | 44 (18–93) | 26 (15–37) | 18 (16–20) | NA | NA | NA | NA | 42 (20–57) | NA | NA | |
| WHO disease classification | |||||||||||||
| DF | 115 | 29 | 27 | 14 | 2 | 0 | 0 | 0 | 0 | 3 | 1‡ | 0 | 190 |
| DHF | 4 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 5 |
| DSS | 1 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 1 |
| Laboratory testing conducted | 47 | 10 | 9 | NA | NA | NA | NA | NA | NA | NA | NA | NA | 66 |
| Leukopenia | 34 | 7 | 5 | NA | NA | NA | NA | NA | NA | NA | NA | NA | 46 |
| Thrombocytopenia | 32 | 5 | 4 | NA | NA | NA | NA | NA | NA | NA | NA | NA | 41 |
| Patient hospitalized | 16 | 10 | 5 | NA | NA | NA | NA | NA | NA | NA | NA | NA | 31 |
| Patient nationality | |||||||||||||
| Senegalese | 46 | 14 | 12 | 14 | 2 | 0 | 0 | 0 | 0 | 2 | 1‡ | 0 | 90 |
| Lebanese | 63 | 2 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 65 |
| Lusophone | 3 | 5 | 12 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 20 |
| French | 7 | 9 | 3 | 0 | 0 | 0 | 0 | 0 | 0 | 1 | 0 | 0 | 20 |
| Chinese | 1 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 1 |
*Values are no. patients except as indicated. NA, not available; WHO, World Health Organization; DF, dengue fever; DHF, dengue hemorrhagic fever; DSS, dengue shock syndrome. †Diourbel, Saint Louis, and Matam. ‡Case identified and diagnosed in Italy.
In conjunction with human testing, mosquito sampling was performed during December 2009 in households with confirmed dengue cases, and entomologic risk indexes (i.e., Breteau and container indices [
Partial DENV envelope protein coding regions were amplified by reverse transcription PCR (
Among the 196 confirmed case-patients, 31 were hospitalized; 5 were found to have dengue hemorrhagic fever (DHF), and 1 died of dengue shock syndrome. The M:F sex ratio for the case-patients was 0.83 (89 male, 107 female), and the median age was 31 years (range 1–93).
The fatal case was in a 71-year-old Lebanese woman hospitalized in a private clinic in Dakar on October 30 with a 4-day history of fever; she had severe thrombocytopenia and elevated transaminase levels. Despite treatment (voluven and adrenaline), she died of cardiac arrest. Disseminated intravascular coagulation was probably responsible for the hemorrhagic syndrome.
Of the 5 other patients (4 Lebanese and 1 Senegalese) who had hemorrhagic manifestations, all had fever, epistaxis, and melena (5/5) associated with thrombocytopenia (platelet count 50–90 × 109/L) and leukopenia (leukocyte count 2.5–3.5 × 109 cells/L); 4 reported headache, and 3 reported myalgia/arthralgia. All 5 patients were hospitalized and received transfusions of fresh frozen plasma, platelet concentrates, and other supportive treatments. Dengue-specific IgM and/or RNA were detected in serum samples collected 2 or 8 days after the onset of symptoms. All patients recovered and were discharged from the hospital after 8 or 10 days.
Using mosquito continuous cell lines, we recovered 49 DENV-3 isolates from confirmed case-patients. Phylogenetic analysis of sequences from mosquito and human samples revealed that DENV-3 genotype III closely related to isolates circulating in Côte d’Ivoire (2008) and China (2009) was circulating during the Senegal outbreak (
Maximum-likelihood phylogenetic tree of dengue virus serotype 3 (D3) sequences from Senegal compared with other sequences. The tree was constructed on the basis of an 885-bp segment of the envelope protein gene. Bootstrap values >70 are labeled next to the node. Sequences from different geographic areas are shown by different colors. Gray shading indicates sequences from Senegal and closely related strains. Scale bar indicates nucleotide substitutions per site.
The entomologic investigation found high epidemic risk in all localities infested with DENV vectors. The Breteau index ranged from 6.6 to 195.2 in Dakar, 1.6 to 32.7 in Louga, and 1.1 to 14.9 in Thies, whereas the container indices ranged from 15 to 63.2 in Dakar, 5.3 to 15.2 in Thies, and 14.3 to 64.2 in Louga. A total of 5,730 mosquitoes were collected; these belonged to 8 species:
An epidemic of DENV-3 occurred in Senegal during September–December 2009; of the 196 laboratory-confirmed cases, most (193) occurred in Dakar. This finding could indicate that transmission rates were higher in this urban area but may have been the result of bias in sample collection; dengue surveillance was less active at health facilities in in other regions, which provided only 277 (39%) of the 696 samples collected from persons who were suspected to have dengue. Fever, headache, myalgia, vomiting, thrombocytopenia, and leukopenia were the most frequent signs and symptoms among patients with confirmed dengue, as described (
The proportion of DHF cases in this outbreak seemed to be high at 3% when compared with previous reports in the Americas from the 1980s through 2007, in which DHF rates ranged from 1.3% to 2.4% (
The percentage of confirmed dengue cases among suspected cases in different communities showed that persons in Senegalese communities were significantly less affected than those in Leebanese (χ2 = 98.3, df = 1; p<0.0001), Lusophone (χ2 = 23.3, df = 1; p<0.0001), and French (χ2 = 11.3, df = 1; p<0.001) communities. Moreover, 5 (83.3%) of the 6 cases with hemorrhagic manifestations occurred in the Lebanese community, which suggests that disease severity might be associated with community exposure.
The phylogenetic analysis of DENV-3 strains isolated during the outbreak suggests that they belong to genotype III and are closely related to DENV-3 isolated from Côte d’Ivoire and China in 2008 and 2009, respectively (
Our findings suggest that increased urban dengue activity is plausible in Senegal. Given ongoing population growth, explosive urbanization, infrastructure building, and international travel, dengue surveillance and preparedness should be reinforced. Furthermore, phylogenetic studies incorporating more DENV-3 strains would shed light on the origins of this DENV-3 outbreak.
We thank Magueye Ndiaye, Modou Diagne, Carlos Fortez, Moussa Dia, and Oumar Ndiaye for excellent technical assistance with laboratory diagnosis and field investigations. We also thank the authorities and the field agents of the Ministry of Health of Senegal for facilitating the investigation of this outbreak.
This work was supported by grants from the Institut Pasteur de Dakar, Senegal; the Ministry of Health of Senegal; and the US National Institutes of Health (grant AI069145).
Dr Ousmane Faye is a virologist and specialist in acarology who works at the Arbovirus and Viral Haemorrhagic Fever Unit, Institut Pasteur de Dakar, Senegal. His primary research interests include the vectorial transmission of arboviruses and viruses causing hemorrhagic fevers.