Mobile Laboratory Reveals the Circulation of Dengue Virus Serotype I of Asian Origin in Medina Gounass (Guediawaye), Senegal
With the growing success of controlling malaria in Sub-Saharan Africa, the incidence of fever due to malaria is in decline, whereas the proportion of patients with non-malaria febrile illness (NMFI) is increasing. Clinical diagnosis of NMFI is hampered by unspecific symptoms, but early diagnosis is...
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| Vydané v: | Diagnostics (Basel) Ročník 10; číslo 6; s. 408 |
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16.06.2020
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| Abstract | With the growing success of controlling malaria in Sub-Saharan Africa, the incidence of fever due to malaria is in decline, whereas the proportion of patients with non-malaria febrile illness (NMFI) is increasing. Clinical diagnosis of NMFI is hampered by unspecific symptoms, but early diagnosis is a key factor for both better patient care and disease control. The aim of this study was to determine the arboviral aetiologies of NMFI in low resource settings, using a mobile laboratory based on recombinase polymerase amplification (RPA) assays. The panel of tests for this study was expanded to five arboviruses: dengue virus (DENV), zika virus (ZIKV), yellow fever virus (YFV), chikungunya virus (CHIKV), and rift valley fever virus (RVFV). One hundred and four children aged between one month and 115 months were enrolled and screened. Three of the 104 blood samples of children <10 years presented at an outpatient clinic tested positive for DENV. The results were confirmed by RT-PCR, partial sequencing, and non-structural protein 1 (NS1) antigen capture by ELISA (Biorad, France). Phylogenetic analysis of the derived DENV-1 sequences clustered them with sequences of DENV-1 isolated from Guangzhou, China, in 2014. In conclusion, this mobile setup proved reliable for the rapid identification of the causative agent of NMFI, with results consistent with those obtained in the reference laboratory’s settings. |
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| AbstractList | With the growing success of controlling malaria in Sub-Saharan Africa, the incidence of fever due to malaria is in decline, whereas the proportion of patients with non-malaria febrile illness (NMFI) is increasing. Clinical diagnosis of NMFI is hampered by unspecific symptoms, but early diagnosis is a key factor for both better patient care and disease control. The aim of this study was to determine the arboviral aetiologies of NMFI in low resource settings, using a mobile laboratory based on recombinase polymerase amplification (RPA) assays. The panel of tests for this study was expanded to five arboviruses: dengue virus (DENV), zika virus (ZIKV), yellow fever virus (YFV), chikungunya virus (CHIKV), and rift valley fever virus (RVFV). One hundred and four children aged between one month and 115 months were enrolled and screened. Three of the 104 blood samples of children <10 years presented at an outpatient clinic tested positive for DENV. The results were confirmed by RT-PCR, partial sequencing, and non-structural protein 1 (NS1) antigen capture by ELISA (Biorad, France). Phylogenetic analysis of the derived DENV-1 sequences clustered them with sequences of DENV-1 isolated from Guangzhou, China, in 2014. In conclusion, this mobile setup proved reliable for the rapid identification of the causative agent of NMFI, with results consistent with those obtained in the reference laboratory’s settings. With the growing success of controlling malaria in Sub-Saharan Africa, the incidence of fever due to malaria is in decline, whereas the proportion of patients with non-malaria febrile illness (NMFI) is increasing. Clinical diagnosis of NMFI is hampered by unspecific symptoms, but early diagnosis is a key factor for both better patient care and disease control. The aim of this study was to determine the arboviral aetiologies of NMFI in low resource settings, using a mobile laboratory based on recombinase polymerase amplification (RPA) assays. The panel of tests for this study was expanded to five arboviruses: dengue virus (DENV), zika virus (ZIKV), yellow fever virus (YFV), chikungunya virus (CHIKV), and rift valley fever virus (RVFV). One hundred and four children aged between one month and 115 months were enrolled and screened. Three of the 104 blood samples of children <10 years presented at an outpatient clinic tested positive for DENV. The results were confirmed by RT-PCR, partial sequencing, and non-structural protein 1 (NS1) antigen capture by ELISA (Biorad, France). Phylogenetic analysis of the derived DENV-1 sequences clustered them with sequences of DENV-1 isolated from Guangzhou, China, in 2014. In conclusion, this mobile setup proved reliable for the rapid identification of the causative agent of NMFI, with results consistent with those obtained in the reference laboratory's settings.With the growing success of controlling malaria in Sub-Saharan Africa, the incidence of fever due to malaria is in decline, whereas the proportion of patients with non-malaria febrile illness (NMFI) is increasing. Clinical diagnosis of NMFI is hampered by unspecific symptoms, but early diagnosis is a key factor for both better patient care and disease control. The aim of this study was to determine the arboviral aetiologies of NMFI in low resource settings, using a mobile laboratory based on recombinase polymerase amplification (RPA) assays. The panel of tests for this study was expanded to five arboviruses: dengue virus (DENV), zika virus (ZIKV), yellow fever virus (YFV), chikungunya virus (CHIKV), and rift valley fever virus (RVFV). One hundred and four children aged between one month and 115 months were enrolled and screened. Three of the 104 blood samples of children <10 years presented at an outpatient clinic tested positive for DENV. The results were confirmed by RT-PCR, partial sequencing, and non-structural protein 1 (NS1) antigen capture by ELISA (Biorad, France). Phylogenetic analysis of the derived DENV-1 sequences clustered them with sequences of DENV-1 isolated from Guangzhou, China, in 2014. In conclusion, this mobile setup proved reliable for the rapid identification of the causative agent of NMFI, with results consistent with those obtained in the reference laboratory's settings. |
| Author | El Wahed, Ahmed Abd Diagne, Cheikh Tidiane Faye, Ousmane Faye, Oumar Weidmann, Manfred Diagne, Moussa Moïse Dieng, Idrissa Richard, Vicent Vray, Muriel Hedible, Boris Gildas Fall, Cheikh Sall, Amadou Alpha |
| AuthorAffiliation | 2 Epidemiology Unit, Institut Pasteur de Dakar, BP220 Dakar, Senegal; ghedible@pasteur.sn (B.G.H.); vrichard@pasteur.nc (V.R.); muriel.vray@pasteur.sn (M.V.) 4 Institute of Aquaculture, University of Stirling, Scotland FK9 4LA, UK; m.w.weidmann@stir.ac.uk 1 Arboviruses and Hemorrhagic Fever Viruses Unit, Virology Department, Institut Pasteur de Dakar, BP220 Dakar, Senegal; idrissa.dieng@pasteur.sn (I.D.); MoussaMoise.Diagne@pasteur.sn (M.M.D.); ct.Diagne@pasteur.sn (C.T.D.); Cheikh.Fall@pasteur.sn (C.F.); Amadou.SALL@pasteur.sn (A.A.S.) 3 Microbiology and Animal Hygiene, University of Goettingen, D-33077 Goettingen, Germany; abdelwahed@dpz.eu |
| AuthorAffiliation_xml | – name: 2 Epidemiology Unit, Institut Pasteur de Dakar, BP220 Dakar, Senegal; ghedible@pasteur.sn (B.G.H.); vrichard@pasteur.nc (V.R.); muriel.vray@pasteur.sn (M.V.) – name: 1 Arboviruses and Hemorrhagic Fever Viruses Unit, Virology Department, Institut Pasteur de Dakar, BP220 Dakar, Senegal; idrissa.dieng@pasteur.sn (I.D.); MoussaMoise.Diagne@pasteur.sn (M.M.D.); ct.Diagne@pasteur.sn (C.T.D.); Cheikh.Fall@pasteur.sn (C.F.); Amadou.SALL@pasteur.sn (A.A.S.) – name: 3 Microbiology and Animal Hygiene, University of Goettingen, D-33077 Goettingen, Germany; abdelwahed@dpz.eu – name: 4 Institute of Aquaculture, University of Stirling, Scotland FK9 4LA, UK; m.w.weidmann@stir.ac.uk |
| Author_xml | – sequence: 1 givenname: Idrissa orcidid: 0000-0002-8584-5592 surname: Dieng fullname: Dieng, Idrissa – sequence: 2 givenname: Boris Gildas surname: Hedible fullname: Hedible, Boris Gildas – sequence: 3 givenname: Moussa Moïse orcidid: 0000-0001-5461-5623 surname: Diagne fullname: Diagne, Moussa Moïse – sequence: 4 givenname: Ahmed Abd surname: El Wahed fullname: El Wahed, Ahmed Abd – sequence: 5 givenname: Cheikh Tidiane orcidid: 0000-0003-2119-9349 surname: Diagne fullname: Diagne, Cheikh Tidiane – sequence: 6 givenname: Cheikh orcidid: 0000-0001-5405-2824 surname: Fall fullname: Fall, Cheikh – sequence: 7 givenname: Vicent surname: Richard fullname: Richard, Vicent – sequence: 8 givenname: Muriel surname: Vray fullname: Vray, Muriel – sequence: 9 givenname: Manfred orcidid: 0000-0002-7063-7491 surname: Weidmann fullname: Weidmann, Manfred – sequence: 10 givenname: Ousmane surname: Faye fullname: Faye, Ousmane – sequence: 11 givenname: Amadou Alpha surname: Sall fullname: Sall, Amadou Alpha – sequence: 12 givenname: Oumar surname: Faye fullname: Faye, Oumar |
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| SubjectTerms | Antibodies Antigens Brief Report Dengue fever DENV Diagnostic tests fever Laboratories Malaria mobile laboratory Mortality NMFI RPA Tropical diseases Viruses |
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| Title | Mobile Laboratory Reveals the Circulation of Dengue Virus Serotype I of Asian Origin in Medina Gounass (Guediawaye), Senegal |
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