Skip to main content
  • Loading metrics

A Historic Report of Zika in Mozambique: Implications for Assessing Current Risk

  • Eduardo Samo Gudo ,

    Affiliation Virus Isolation Laboratory, National Institute of Health, Ministry of Health, Maputo, Mozambique

  • Kerstin I. Falk,

    Affiliations Department of Microbiology, The Public Health Agency of Sweden, Solna, Sweden, Department of Microbiology, Tumor and Cell Biology, Karolinska Institute, Solna, Sweden

  • Sadia Ali,

    Affiliation Virus Isolation Laboratory, National Institute of Health, Ministry of Health, Maputo, Mozambique

  • Argentina Felisbela Muianga,

    Affiliation Virus Isolation Laboratory, National Institute of Health, Ministry of Health, Maputo, Mozambique

  • Vanessa Monteiro,

    Affiliation Virus Isolation Laboratory, National Institute of Health, Ministry of Health, Maputo, Mozambique

  • Julie Cliff

    Affiliation Community Health Department, Faculty of Medicine, Eduardo Mondlane University, Maputo, Mozambique


Zika virus (ZIKV) is an arthropod-borne flavivirus transmitted to humans by the bite of the Aedes mosquito. The virus was first isolated in 1947 from a rhesus monkey in the Zika forest in Uganda [1].

For more than half a century, the virus was confined to Africa and Asia, and only 14 human cases of Zika had been documented [2]. This changed in 2007 when an outbreak was reported on Yap Island in Micronesia [3, 4], followed by a large epidemic in French Polynesia in 2013 [5, 6]. More recently, ZIKV has spread explosively in South and Central America and the Caribbean [2, 7]. Reports of associated microcephaly cases and other neurologic disorders in Brazil and a similar cluster in French Polynesia in 2014 led WHO to declare a Public Health Emergency of International Concern (PHEIC) on February 1st, 2016 [8].

To prevent globalization of ZIKV, WHO developed a Zika strategic response framework. They recommended that unaffected countries rapidly assess their risk of being hit by ZIKV [9] in order to develop preparedness plans. The fear of ZIKV is attributed to the fact that not only has Aedes, the main vector of ZIKV, spread exponentially over the world in the last decades but also because of the large number of susceptible populations worldwide and the absence of an effective vaccine [9, 10].

Zika in Sub-Saharan Africa

The sub-Saharan Africa region where the first cases of Zika in humans were initially reported is the least prepared but is at most risk. Since its discovery in 1947, sporadic cases of Zika have been reported in several countries in sub-Saharan Africa [2]. So far in sub-Saharan Africa, only Cape Verde has reported a recent outbreak, with more than 5,000 suspected cases [11].

However, for several decades the presence of ZIKV was only sporadically studied in Southern Africa, since Zika was considered a benign disease with a low public health importance. In addition, few countries have performed mapping of the distribution of Aedes, which represents an important gap in assessing the risk of spread of the virus to these countries. Most of the reported human cases of Zika are situated in Central, East, and West Africa [1, 1219].

With regard to the Southern Africa region, serosurveys have been conducted in Angola, Tanzania, Zambia, and Mozambique, which have found positive results for ZIKV; no other data are available [2]. However, most of these studies are quite old and most were conducted between the 1960s and 1990s [2].

Past History of Zika in Mozambique and Implication for Assessing Current Risk

Although Kokernot et al. found neutralizing antibodies against ZIKV in Mozambique in 1957 [20], the country has repeatedly been excluded from the list of countries with a past history of ZIKV. The current Centers for Disease Control and Prevention map, the recent World Health Organization Risk Assessment map on ZIKV in the Africa region, and most of the recent literature mapping countries with a current and past history of ZIKV have consistently excluded Mozambique [10, 21, 22] from the list of countries with past serological evidence of ZIKV. This might result in errors in the calculation and interpretation of the risk of Zika in Mozambique as well as in the region. In this regard, in this manuscript we revisit findings of the study conducted by Kokernot et al. in an attempt to discuss the current risk of Zika in the country. The survey, conducted in 1957, was published in Portuguese in 1960 [20].

This study was part of a larger study on arboviruses, in which blood samples were screened for antibodies against 13 arboviruses, including ZIKV, chikungunya, Rift Valley fever, Sindbis, Middleburg, and Wesselsbron. Samples were collected in 29 localities situated widely apart from each other throughout the country between July and August 1957. In each locality, they selected an average of 30 local residents who had been born in the area with no history of travel outside in their lifetime.

The samples were analyzed in South Africa, using confirmatory neutralization testing (NT). NT was performed using an in vivo system. For this purpose, previously titrated virus strains for each arbovirus being tested were incubated with each participant’s serum and inoculated into Swiss mice to assess the neutralization profile of each serum against each virus strain. For ZIKV, the prototype ZIKV strain was used [18], and both adult and newborn mice were used for inoculation. An amount of 0.03 mL of the preparation virus and serum was inoculated intracerebrally, as previously described [18], and each mouse was observed daily between 10–17 days to assess the viral effect.

The authors found neutralizing antibodies to all of the viruses and concluded that the whole length of Mozambique was a “tropical corridor” of arbovirus activity. The viruses with highest prevalence rates of neutralizing antibodies were chikungunya (21.0%), Wesselsbron (15.9%), Bunyamwera (24.1%), Pongola (23.2%) and Bwamba fever (24.7%).

ZIKV was tested for in a more limited number of samples from 22 localities (see Fig 1). Of a total of 249 samples (152 adults, 107 children) tested, the overall prevalence was 4.0% (10/249). Serological findings were analyzed by age, geographical distribution, and altitude. The highest prevalence rate—9.8% (6/61)—was found in adults living in areas below 200 m north of the Zambezi river. The ZIKV seroprevalence rate was lower in children: 1.0% (2/107) compared to 5.6% (8/152) in adults. Neutralizing antibodies against ZIKV were found in nine localities (see Fig 1). For adults, they were found in seven localities—namely, Guijá (1/1), Sena (1/13), Mualama (2/11), Nametil (1/9), Lumbo (1/15), and Quissanga (2/13). For children, antibodies were found in two localities—namely, Marromeu (1/5) and Belua (1/1). The prevalence rate was slightly higher south of the Zambezi river compared to north of the river (4.2%, 3/71 south versus 3.9%, 7/178 north). This study also showed that the prevalence of ZIKV was higher in places situated at an altitude between 0–200 m (5.2%, 9/173) compared with those situated between 200–1000m (1.3%, 1/73).

Fig 1.

Geographical distribution of districts where study was conducted and where neutralizing antibodies against Zika were found during the Kokernot et al. study in 1957 (panel A) and where recent outbreaks of Dengue were reported (panel B). Credit: Américo Feriano José.

These findings should be interpreted with caution, as cross-reaction between flaviviruses has been reported in NT assays. To help clarify this issue, we revisited carefully the original manuscript of ZIKV isolation published by Dick et al. in 1952 [18] and noted that dengue immune serum had no relevant neutralizing effect on ZIKV using an in vivo NT assay similar to that used by Kokernot et al. [18].

Our belief is that the manuscript published by Kokernot et al. has been consistently ignored in most of the international literature because although the title of the manuscript is available in English on PubMed, it is not found using keywords such as “arbovirus and Mozambique” or “Zika and Mozambique,” possibly because of deficient indexing of old articles.

Old literature is relevant, particularly at a time when countries are developing their national preparedness plan for Zika and microcephaly. In this regard, the exclusion of Mozambique from the list of countries with past history of serological evidence of ZIKV might hamper national and international efforts to prevent Zika and microcephaly in the country.

While the 1957 study in Mozambique suggests that ZIKV may have circulated in the past, we cannot assume that the virus is still present. No further studies have been conducted in Mozambique, which limits our discussion on whether the virus may have been eliminated during the efforts in the 1970s and 1980s to reduce the malaria burden through massive distribution of bed nets, community education, indoor and outdoor spraying campaigns, and appropriate malaria case management, among others [23, 24]. Whether efforts to reduce the burden of Anopheles mosquitoes in Mozambique resulted in any impact in the population of Aedes is unknown as, for several decades, most entomological investigation in Mozambique was restricted to Anopheles. During these decades, Aedes was never considered during vector surveillance activities until recently, when a dengue outbreak hit two provinces in northern Mozambique and Aedes was found to be abundant in northern Mozambique [25].

Whether the past evidence of antibodies against ZIKV in Mozambique suggests that the country is vulnerable to the current virus strain circulating in the Americas is not known. The ZIKV has evolved since it was first isolated in Uganda in 1947 [14, 26]. The African lineage is slightly different from those circulating in Asia and the Americas [2, 14]. Whether the African lineages of ZIKV have a lower ability to spread and cause outbreaks or epidemics in sub-Saharan Africa is still a matter of debate.

On the other hand, the initial descriptions of ZIKV in mosquitoes were linked to other species of Aedes, such as Aedes africanus, A. furcifer, A. taylori, and A. luteocephalus [27]. The occurrence of sporadic human cases of Zika reported in West and Central Africa, and the absence of cases further south, may suggest lower virus competence. Notably, a recent study on Aedes competence to assess its ability for transmitting ZIKV found that Aedes had a lower to null competence to transmit the virus [28]. Chouin-Carneiro et al. had a recent publication in which they found a lower competence of both A. aegypti and A. albopticus from the Americas in transmitting ZIKV [29]. A recent editorial in the South African Medical Journal on the risk of Zika in South Africa observed that prediction models using the distribution of A. aegypti do not place that country at high risk [30].

Kokernot et al.’s serosurvey was accompanied by a survey for culicine mosquitoes [31]. The results, published with a review of other information, showed that Aedes was present in many locations in Mozambique. They included a published study conducted in 1959 and 1960 in Lumbo, situated in northern Mozambique, which found Aedes [32]. Our recent study conducted in April 2014 in four large cities in Mozambique and aiming to investigate the presence and abundance of the Aedes mosquito found that Aedes occurred in all four cities. The cities were Pemba, Nampula, and Nacala in northern Mozambique and the capital of Maputo Province in southern Mozambique [33]. The proportions of sampled tires containing Aedes aegypti were 72.0% in Pemba, 59.0% in Nampula, and 64.5% in Nacala, compared to 19.3% in Maputo Province. Thus, Aedes aegypti was more abundant in the three northern cities compared to the southern [33]. The greater abundance of Aedes aegypti together with a higher proportion of Aedes in the northern cities suggests that arboviral transmission may be greater in northern Mozambique. To date, outbreaks of dengue have only been reported from northern Mozambique [25, 34]. This suggests that the risk of Zika may be higher in northern compared to southern Mozambique.

Taken together, the historical data on Zika, a recent outbreak of dengue [25], and the recent detection of chikungunya antibodies in febrile patients in southern Mozambique [35] highlight an urgent need to implement vector surveillance and control of Aedes mosquitoes as part of arbovirus control in Mozambique. Aedes surveillance and control activities have been heavily neglected in Mozambique in recent decades, with entomological interventions entirely focused on malaria. Since vector surveillance and control activities for malaria are well established in Mozambique, we recommend that Aedes control activities should be integrated into the existing activities for malaria control in order to maximize the scarce resources. Our findings also suggest that particular attention should be given to provinces situated in northern Mozambique, where arboviral transmission is probably higher.

The recent confirmation of sexual transmission of ZIKV [3638] poses a serious concern for countries with a high incidence of sexually transmitted diseases such as Mozambique, which occupies the eighth position among the countries with the highest HIV-1/2 prevalence in the world [39, 40]. In addition to spread through an abundance of Aedes, the risk of spread through unprotected sexual intercourse should be taken into account.

In regard to Mozambique, no study on vector competence has been conducted so far, which limits our discussion related to vector competence of A. aegypti circulating in Mozambique. In this regard, although our recent publication showed that Aedes mosquitoes were abundant in northern Mozambique [25] and another recent publication also by our group showed that A. albopictus circulates in southern Mozambique [41], studies of vector competence of Aedes mosquitoes are urgently needed to assess the ability of the Aedes strains in Mozambique to transmit the current virus strain circulating in the Americas. Moreover, genetic variations of Aedes mosquitoes have been shown to lead to variations in the ability of Aedes to transmit arbovirus [42, 43]. The literature shows that Aedes is highly prevalent in most sub-Saharan African countries, including those that share borders with Mozambique [4448].

In conclusion, this manuscript combines historic data with recent findings to suggest that arboviral activity may be intense in Mozambique, particularly in the northern part of the country where Aedes is abundant and past and recent outbreaks of dengue have been reported. The historic findings reported by Kokernot et al. provide sufficient evidence to include Mozambique in the list of countries at risk of Zika and in need of immediate interventions to generate the missing evidence needed for the design of effective prevention strategies. In view of these findings and taking into consideration the scarcity of funds for arboviral related interventions, we propose (i) incorporation of entomological surveillance for Aedes within the framework of existing entomological surveillance for malaria vectors, (ii) incorporation of surveillance for arboviruses within the existing surveillance system for endemic diseases, and (iii) integration of Aedes control interventions within the existing framework for controlling the malaria vector. Integration of interventions for surveillance and control of malaria and arboviruses should take into consideration the specificities and difference of the ecology of Anopheles and Aedes mosquitoes.


We thank Prof Janus Paweska and Jacqueline Weyer from the National Institute of Communicable Disease, South Africa, for sharing their recent manuscript addressing assessment of risk of Zika in South Africa.


  1. 1. Simpson DI. Zika Virus Infection in Man. Trans R Soc Trop Med Hyg. 1964;58:335–8. pmid:14175744
  2. 2. Musso D, Gubler DJ. Zika Virus. Clin Microbiol Rev. 2016;29(3):487–524. pmid:27029595
  3. 3. Duffy MR, Chen TH, Hancock WT, Powers AM, Kool JL, Lanciotti RS, et al. Zika virus outbreak on Yap Island, Federated States of Micronesia. N Engl J Med. 2009;360(24):2536–43. pmid:19516034
  4. 4. Lanciotti RS, Kosoy OL, Laven JJ, Velez JO, Lambert AJ, Johnson AJ, et al. Genetic and serologic properties of Zika virus associated with an epidemic, Yap State, Micronesia, 2007. Emerg Infect Dis. 2008;14(8):1232–9. PubMed Central PMCID: PMC2600394. pmid:18680646
  5. 5. Cao-Lormeau VM, Roche C, Teissier A, Robin E, Berry AL, Mallet HP, et al. Zika virus, French polynesia, South pacific, 2013. Emerg Infect Dis. 2014;20(6):1085–6. PubMed Central PMCID: PMCPMC4036769. pmid:24856001
  6. 6. Ioos S, Mallet HP, Leparc Goffart I, Gauthier V, Cardoso T, Herida M. Current Zika virus epidemiology and recent epidemics. Med Mal Infect. 2014;44(7):302–7. pmid:25001879
  7. 7. Chang C, Ortiz K, Ansari A, Gershwin ME. The Zika outbreak of the 21st century. J Autoimmun. 2016;68:1–13. pmid:26925496
  8. 8. World Health Organization. WHO Director-General summarizes the outcome of the Emergency Committee regarding clusters of microcephaly and Guillain-Barré syndrome. 2016 [cited April 14, 2016].
  10. 10. Gyawali N, Bradbury RS, Taylor-Robinson AW. The global spread of Zika virus: is public and media concern justified in regions currently unaffected? Infect Dis Poverty. 2016;5(1):37. PubMed Central PMCID: PMCPMC4837632.
  11. 11. World Health Organization. Zika virus infection–Cape Verde. 2015.
  12. 12. Diallo D, Sall AA, Diagne CT, Faye O, Faye O, Ba Y, et al. Zika virus emergence in mosquitoes in southeastern Senegal, 2011. PLoS ONE. 2014;9(10):e109442. PubMed Central PMCID: PMC4195678. pmid:25310102
  13. 13. Fagbami AH. Zika virus infections in Nigeria: virological and seroepidemiological investigations in Oyo State. The Journal of hygiene. 1979;83(2):213–9. PubMed Central PMCID: PMC2129900. pmid:489960
  14. 14. Grard G, Caron M, Mombo IM, Nkoghe D, Mboui Ondo S, Jiolle D, et al. Zika virus in Gabon (Central Africa)—2007: a new threat from Aedes albopictus? PLoS Negl Trop Dis. 2014;8(2):e2681. PubMed Central PMCID: PMC3916288. pmid:24516683
  15. 15. Monlun E, Zeller H, Le Guenno B, Traore-Lamizana M, Hervy JP, Adam F, et al. [Surveillance of the circulation of arbovirus of medical interest in the region of eastern Senegal]. Bull Soc Pathol Exot. 1993;86(1):21–8. pmid:8099299
  16. 16. Moore DL, Causey OR, Carey DE, Reddy S, Cooke AR, Akinkugbe FM, et al. Arthropod-borne viral infections of man in Nigeria, 1964–1970. Ann Trop Med Parasitol. 1975;69(1):49–64. pmid:1124969
  17. 17. Akoua-Koffi C, Diarrassouba S, Benie VB, Ngbichi JM, Bozoua T, Bosson A, et al. [Investigation surrounding a fatal case of yellow fever in Cote d'Ivoire in 1999]. Bull Soc Pathol Exot. 2001;94(3):227–30. pmid:11681215
  18. 18. Dick GW, Kitchen SF, Haddow AJ. Zika virus. I. Isolations and serological specificity. Trans R Soc Trop Med Hyg. 1952;46(5):509–20. pmid:12995440
  19. 19. Haddow AJ, Williams MC, Woodall JP, Simpson DI, Goma LK. Twelve Isolations of Zika Virus from Aedes (Stegomyia) Africanus (Theobald) Taken in and above a Uganda Forest. Bull World Health Organ. 1964;31:57–69. PubMed Central PMCID: PMC2555143. pmid:14230895
  20. 20. Kokernot RH, Smithburn KC, Gandara AF, McIntosh BM, Heymann CS. [Neutralization tests with sera from individuals residing in Mozambique against specific viruses isolated in Africa, transmitted by arthropods]. An Inst Med Trop (Lisb) 1960 Jan-Jun; 17:201–30. and
  21. 21. Centers for Disease Control and Prevention. Countries that have past or current evidence of Zika virus transmission (as of January 2016). April 14, 2016.
  22. 22. World Health Organization ROfA. Zika Virus Risk Assessment in the WHO African region: A Technical Report. World Health Organization, Regional Office for Africa, 2016.
  23. 23. Mabaso ML, Sharp B, Lengeler C. Historical review of malarial control in southern African with emphasis on the use of indoor residual house-spraying. Trop Med Int Health. 2004;9(8):846–56. pmid:15303988
  24. 24. Sharp BL, Kleinschmidt I, Streat E, Maharaj R, Barnes KI, Durrheim DN, et al. Seven years of regional malaria control collaboration—Mozambique, South Africa, and Swaziland. Am J Trop Med Hyg. 2007;76(1):42–7. PubMed Central PMCID: PMC3749812. pmid:17255227
  25. 25. Massangaie M, Pinto G, Padama F, Chambe G, da Silva M, Mate I, et al. Clinical and Epidemiological Characterization of the First Recognized Outbreak of Dengue Virus-Type 2 in Mozambique, 2014. Am J Trop Med Hyg. 2016:94(2):413–6. pmid:26643534
  26. 26. Haddow AD, Schuh AJ, Yasuda CY, Kasper MR, Heang V, Huy R, et al. Genetic characterization of Zika virus strains: geographic expansion of the Asian lineage. PLoS Negl Trop Dis. 2012;6(2):e1477. PubMed Central PMCID: PMC3289602. pmid:22389730
  27. 27. Hayes EB. Zika virus outside Africa. Emerg Infect Dis. 2009;15(9):1347–50. PubMed Central PMCID: PMC2819875. pmid:19788800
  28. 28. Diagne CT, Diallo D, Faye O, Ba Y, Faye O, Gaye A, et al. Potential of selected Senegalese Aedes spp. mosquitoes (Diptera: Culicidae) to transmit Zika virus. BMC Infect Dis. 2015;15:492. PubMed Central PMCID: PMCPMC4629289. pmid:26527535
  29. 29. Chouin-Carneiro T, Vega-Rua A, Vazeille M, Yebakima A, Girod R, Goindin D, et al. Differential Susceptibilities of Aedes aegypti and Aedes albopictus from the Americas to Zika Virus. PLoS Negl Trop Dis. 2016;10(3):e0004543. PubMed Central PMCID: PMCPMC4777396. pmid:26938868
  30. 30. Jansen van Vuren P, Weyer J, Kemp A, Dermaux-Msimang V, McCarthy K, Blumberg L, et al. Is South Africa at risk for Zika virus disease? S Afr Med J. 2016;106(3):232–3. pmid:26915933
  31. 31. Worth CB, de Meillon B. Culicine mosquitoes (Diptera: Culicidae) recorded from the province of Mozambique (Portuguese East Africa) and their relationship to arthropod-borne viruses. An Inst Med Trop (Lisb). 1960;17:231–56.
  32. 32. Kokernot RH, McIntosh B, Worth CB, De Morais T, Weinbren MP. Isolation of viruses from mosquitoes collected at Lumbo, Mozambique. I. Lumbo virus, a new virus isolated from Aedes (Skusea) pembaensis Theobald. Am J Trop Med Hyg. 1962;11:678–82. pmid:14034311
  33. 33. Higa Y, Abilio AP, Futami K, Lazaro MA, Minakawa N, Gudo ES. Abundant Aedes (Stegomyia) aegypti aegypti mosquitoes in the 2014 dengue outbreak area of Mozambique. Tropical medicine and health. 2015;43(2):107–9. PubMed Central PMCID: PMC4458510. pmid:26060423
  34. 34. Gubler DJ, Sather GE, Kuno G, Cabral JR. Dengue 3 virus transmission in Africa. Am J Trop Med Hyg. 1986;35(6):1280–4. pmid:3789276
  35. 35. Gudo ES, Pinto G, Vene S, Mandlaze A, Muianga AF, Cliff J, et al. Serological evidence of chikungunya virus among acute febrile patients in Southern Mozambique. PLoS Negl Trop Dis. 2015;9(10):e0004146. pmid:26473605
  36. 36. Frank C, Cadar D, Schlaphof A, Neddersen N, Gunther S, Schmidt-Chanasit J, et al. Sexual transmission of Zika virus in Germany, April 2016. Euro Surveill. 2016;21(23).
  37. 37. Harrower J, Kiedrzynski T, Baker S, Upton A, Rahnama F, Sherwood J, et al. Sexual Transmission of Zika Virus and Persistence in Semen, New Zealand, 2016. Emerg Infect Dis. 2016;22(10)1855–7. pmid:27454745
  38. 38. Moreira J, Lamas CC, Siqueira A. Sexual transmission of Zika virus: implications for clinical care and public health policy. Clin Infect Dis. 2016;63(1):141–2 pmid:27048746
  39. 39. Saúde INd, Estatística INd, Macro I. Inquérito Nacional de Prevalência, Riscos Comportamentais e Informação sobre o HIV e SIDA em Moçambique—INSIDA 2009. Maputo, Mozambique: 2010.
  40. 40. UNAIDS. UNAIDS report on the global AIDS epidemic 2013. 2013.
  41. 41. Kampango A, Abilio AP. The Asian tiger hunts in Maputo city-the first confirmed report of Aedes (Stegomyia) albopictus (Skuse, 1895) in Mozambique. Parasit Vectors. 2016;9(1):76. PubMed Central PMCID: PMCPMC4746916.
  42. 42. Failloux AB, Vazeille M, Rodhain F. Geographic genetic variation in populations of the dengue virus vector Aedes aegypti. J Mol Evol. 2002;55(6):653–63. pmid:12486524
  43. 43. Tesh RB, Gubler DJ, Rosen L. Variation among goegraphic strains of Aedes albopictus in susceptibility to infection with chikungunya virus. Am J Trop Med Hyg. 1976;25(2):326–35. pmid:1259092
  44. 44. Jupp PG, Kemp A. The potential for dengue in South Africa: vector competence tests with dengue 1 and 2 viruses and 6 mosquito species. Trans R Soc Trop Med Hyg. 1993;87(6):639–43. pmid:7905212
  45. 45. Mboera LE, Mweya CN, Rumisha SF, Tungu PK, Stanley G, Makange MR, et al. The Risk of Dengue Virus Transmission in Dar es Salaam, Tanzania during an Epidemic Period of 2014. PLoS Negl Trop Dis. 2016;10(1):e0004313. PubMed Central PMCID: PMCPMC4728062. pmid:26812489
  46. 46. Mweya CN, Kimera SI, Mellau LS, Mboera LE. Inter-epidemic abundance and distribution of potential mosquito vectors for Rift Valley fever virus in Ngorongoro district, Tanzania. Global health action. 2015;8:25929. PubMed Central PMCID: PMCPMC4303619. pmid:25613346
  47. 47. Masaninga F, Muleba M, Masendu H, Songolo P, Mweene-Ndumba I, Mazaba-Liwewe ML, et al. Distribution of yellow fever vectors in Northwestern and Western Provinces, Zambia. Asian Pac J Trop Med. 2014;7S1:S88–92. pmid:25312199
  48. 48. Meda N, Sara Salinas, Kagoné T, Simonin Y, Perre PVd. Zika virus epidemic: Africa should not be neglected. The Lancet. 2016;388(10042):337–8.