The impact of residual infections on Anopheles-transmitted Wuchereria bancrofti after multiple rounds of mass drug administration
© de Souza et al. 2015
Received: 28 July 2015
Accepted: 11 September 2015
Published: 24 September 2015
Many countries have made significant progress in the implementation of World Health Organization recommended preventive chemotherapy strategy, to eliminate lymphatic filariasis (LF). However, pertinent challenges such as the existence of areas of residual infections in disease endemic districts pose potential threats to the achievements made. Thus, this study was undertaken to assess the importance of these areas in implementation units (districts) where microfilaria (MF) positive individuals could not be found during the mid-term assessment after three rounds of mass drug administration.
This study was undertaken in Bo and Pujehun, two LF endemic districts of Sierra Leone, with baseline MF prevalence of 2 % and 0 % respectively in sentinel sites for monitoring impact of the national programme. Study communities in the districts were purposefully selected and an assessment of LF infection prevalence was conducted together with entomological investigations undertaken to determine the existence of areas with residual MF that could enable transmission by local vectors. The transmission Assessment Survey (TAS) protocol described by WHO was applied in the two districts to determine infection of LF in 6–7 year old children who were born before MDA against LF started.
The results indicated the presence of MF infected children in Pujehun district. An. gambiae collected in the district were also positive for W. bancrofti, even though the prevalence of infection was below the threshold associated with active transmission.
Residual infection was detected after three rounds of MDA in Pujehun – a district of 0 % Mf prevalence at the sentinel site. Nevertheless, our results showed that the transmission was contained in a small area. With the scale up of vector control in Anopheles transmission zones, some areas of residual infection may not pose a serious threat for the resurgence of LF if the prevalence of infections observed during TAS are below the threshold required for active transmission of the parasite. However, robust surveillance strategies capable of detecting residual infections must be implemented, together with entomological assessments to determine if ongoing vector control activities, biting rates and infection rates of the vectors can support the transmission of the disease. Furthermore, in areas where mid-term assessments reveal MF prevalence below 1 % or 2 % antigen level, in Anopheles transmission areas with active and effective malaria vector control efforts, the minimum 5 rounds of MDA may not be required before implementing TAS. Thus, we propose a modification of the WHO recommendation for the timing of sentinel and spot-check site assessments in national programs.
The Global Program to Eliminate Lymphatic Filariasis (GPELF) targets the elimination of LF as a public health problem by the year 2020, through mass drug administration (MDA) in endemic implementation units (IU), with the aim of interrupting transmission and stopping the spread of infection in all endemic areas. . While many countries have made significant progress in reducing transmission intensity and incidence of infection through community-wide treatments, there remain significant programmatic challenges to interrupting parasite transmission. These include effective implementation of the preventive chemotherapy strategy in urban settings, [2, 3] and the existence of areas of residual infection [4–6] that may precipitate the spread of infection after the conditions for stopping MDA have been met [7, 8].
Implementing MDA is a critical challenge for the GPELF, especially in countries affected by conflict. Among the four LF endemic countries (Sierra Leone, Liberia, Guinea and Cote d’Ivoire) recently affected by conflict in West Africa, only Sierra Leone was implementing MDA (with Ivermectin and Albendazole) in 2011. All 14 districts in Sierra Leone were endemic for LF antigen before MDA started in 2008 [9, 10]. Nevertheless, after three rounds of treatment (2008–2010), a midterm progress evaluation following WHO guidelines revealed that the microfilaria prevalence in people five years and older was reduced to 0 % in five districts . The other nine districts had microfilaria (MF) prevalence below 1 % in sentinel sites with the exception of one district. The overall average MF prevalence, before and after the three MDAs, were 2.4 % and 0.3 % respectively .
LF and onchocerciasis are co-endemic in 12 of the 14 districts in Sierra Leone. Prior to the initiation of MDA for LF in Sierra Leone in 2007, many people in the implementation units co-endemic for both diseases had received more than 5 rounds of treatment with Ivermectin through the community directed intervention (CDI) implemented by the African Programme for Onchocerciasis Control (APOC) . Treatment for onchocerciasis and, scaling up of bed net distribution in Sierra Leone [12, 13] may have impacted LF prevalence because Ivermectin alone is also effective against LF [14–16], and treated bed nets dramatically reduce exposure to mosquito bites . Furthermore, in Sierra Leone as in other countries in West Africa, LF is transmitted solely by the malaria carrying Anopheles mosquitoes . Anopheles-transmitted LF is highly focal [19–21] and synchronous with intense malaria transmission [21, 22]. Malaria control efforts targeting Anopheles mosquitoes therefore have the potential to significantly impact on LF transmission in West Africa, as was possibly the case in the interruption of LF transmission in Togo .
WHO recommends that a Transmission Assessment Survey (TAS) to determine when to stop MDA be carried out when an implementation unit (District) has completed five effective rounds of annual MDA and the prevalence of MF is less than 1 % in all sentinel and spot check sites in the districts . TAS is based on antigenemia prevalence (in children) that may persist after transmission has been interrupted. Interpretation of these endpoints is also confounded by the size of the evaluation unit, focality of the disease and movement of infected individuals from endemic areas to non-endemic areas. Despite the fact that Sierra Leone had only implemented three effective rounds of MDA for LF, this study was undertaken to investigate the significance of residual infections for the outcome of TAS in areas of Anopheles-transmitted LF previously treated with Ivermectin, and with active vector control activities.
Approval for the study was obtained from the ethics review committee of the Liverpool School of Tropical Medicine and the Ministry of Health – Sierra Leone. Prior to conducting the survey and obtaining informed consent, repeated community meetings were held in all of the villages to communicate the purposes of the study and answer questions at the individual and community level. Informed consent to participate in the study was obtained from all individuals 18 years or older. Consent was obtained from a parent or guardian of younger individuals. Informed consent was also received from mosquito collectors, 18 years and above, after which they were trained in safe and scientifically reliable mosquito collection. Consent was also sought from the head of the households where mosquito sampling was carried out.
For the Transmission Assessment Surveys (TAS), the communities where the schools were located were informed of the purpose of the study, in their local language. Due to low literacy rates, informed oral consent was obtained from the community leaders, as well as parents and guardians of each child participating in the study. The names of consenting parents and their children were recorded, and only the principal investigators of the study had access to this information. The data was analysed and reported, to exclude any directly identifiable information, in order to maintain the anonymity of the parents and children.
Surveillance for LF in study sites in Pujehun and Bo Districts. *Schools in these communities were part of the TAS survey
ICT Positive (%)
Assessment for LF prevalence was conducted in the study communities using the Binax Now ICT card. Altogether, 1542 individuals were surveyed in the Pujehun District while 1313 individuals were surveyed in the Bo District. Samples were collected from individuals aged between 6–65 years of age.
Entomological surveys were also undertaken to determine the existence of active transmission in study areas, and also study the importance of local transmission. Thus, mosquitoes were collected using the Pyrethrum Spray method, Exit Traps and Human Landing Collections, and processed as previously described . Briefly, DNA was extracted from pooled mosquitoes using the Qiagen DNeasy tissue kit (Qiagen CA) extraction method. This was followed by PCR to detect W. bancrofti DNA using the method of Ramzy and colleagues . A positive and negative control was included in all reactions and samples testing positive for W. bancrofti were confirmed using a second PCR. Positive samples were also confirmed using the slightly modified loop-mediated isothermal amplification (LAMP) method for detecting W. bancrofti DNA . In each household surveyed for mosquitoes, we collected information on the number of people living in the house and the number of people who used ITN the night before the collection. From this information ITN usage rates were determined for each community.
While this study was not meant to undertake Transmission Assessment Surveys (TAS) , the TAS protocol was applied in the two districts because it is a statistically strong method to determine infection prevalence of LF in children as an indicator of active transmission in the district. TAS for LF is undertaken to determine whether infection has been reduced to levels below which transmission cannot be sustained, allowing for a decision to stop MDA. As such, children aged 6–7 years were sampled from various schools selected using the TAS protocol, and tested for LF antigen and microfilaria. Some schools in the LF assessment sites formed part of the schools selected using the TAS protocol.
Infection in the vector population was calculated using the Poolscreen v2.0  to determine the maximum likelihood of infection together with the associated 95 % CIs. From the ICT and TAS survey, the prevalence (%) of antigenemia and microfilaremia was calculated as the number of positive people divided by the number of people examined.
The cross sectional surveys revealed that out of the six communities surveyed in Pujehun district, three were positive for W. bancrofti infection using ICT cards (Table 1). In Bo, two communities out of four were positive for antigen. The total antigen prevalence in the districts was 0.3 % (5/1542) and 0.7 % (9/1313) in the Pujehun and Bo districts respectively.
TAS summary results for school children in Pujehun and Bo Districts 
No. of Schools
No. of Children Surveyed
No. MF Positive
No. Ag. Positive (%)
Critical Cut-off Value for Ag positives
659 (43.8 %)
844 (56.2 %)
10 (0.67 %)
682 (43.6 %)
882 (56.4 %)
3 (0.16 %)
School clusters positive during the TAS survey
Names of schools
No. of Ag. Positives (%)
No. of MF Positives (%)
Roman Catholic school
United Muslim Association
3 (7.1 %)
SLC Primary School
SLC Primary School
SLC Primary School
Roman Catholic school
UMC Primary School
Xenomonitoring results from Pujehun and Bo Districts
ITN Usage (%)
No. of mosquitoes
No. of pools
Pools positive (MLI %)
95 % CI
0.044 - 7.1
0.064 - 10.1
0.094 - 2.76
The results of the antigen prevalence survey revealed that levels were below the thresholds that signify sustainable transmission . However, it is worth mentioning that even though the antigen levels were below the recommended levels for the entire districts, antigen levels were ≥ 2 % in some of the school clusters used in the TAS protocol, with similar observations made in Sri Lanka and Zanzibar [5, 29]. During the mapping surveys in 2008, Pujehun was one of the districts with low endemicity of antigenemia (4 %), with no microfilaria detected . Nonetheless, our study revealed the existence of areas with residual transmission in Pujehun district with evidence of active but highly focal transmission of LF through the detection of MF in children and uptake of MF by LF vectors. While areas of residual transmission may be termed as hotspots, it is important to clearly establish what can be considered a hotspot in LF transmission. We considered a hotspot to be: 1. an area where MF carriers persisted after 3 or more rounds of MDA when the sentinel site prevalence is less than 1 %; 2. school clusters with antigen prevalence of > 2 % in 6–7 year olds, following TAS. The existence of areas of residual transmission in Pujehun District (Fig. 1) illustrates the focality of Anopheles-transmitted LF and challenges faced in selecting high risk areas for sentinel site and spot check surveys, and the need for adopting more statistically robust sampling strategies and reviewing the size of the evaluation unit for TAS .
The low numbers of mosquitoes collected in the study areas is probably the result of the high ITN usage in the study areas (66.1 % and 49.3 % in Pujehun and Bo respectively). There has been an increased use of insecticide treated nets through mass ITN distribution campaigns in Sierra Leone and in the Pujehun and Bo Districts [12, 13]. By 2010, 67.2 % LLIN usage was reported in the study areas . Prior to this, the use of ITN has never been tried in forest zones, and the introduction of ITN in Bo district followed earlier studies to evaluate the Anopheline ecology and behaviour, to understand the role of the vectors in malaria epidemiology and formulate appropriate strategies for the area [30–33].
The detection of positive mosquitoes in areas positive for antigen in humans indicates possible on-going transmission, and similar results have been obtained in the American Samoa . These results support the evidence that molecular xenomonitoring can be an effective tool in post-MDA surveillance [5, 34]. While there is currently no existing target threshold for monitoring parasite DNA prevalence in Anopheline vectors [5, 35], 0.25 % has been suggested as the maximum infection prevalence expected to sustain transmission by Culex species . Studies are required to determine cut-off threshold for Anopheles mosquitoes. Further, given that Culex mosquitoes are more efficient LF vectors than Anopheles, we advocate the establishment for different cut-offs for these species by TAS, as the current algorithm for choosing TAS design is similar in areas where LF is transmitted by Anopheles and Culex species .
In Sierra Leone, as in the other countries in West Africa, lymphatic filariasis is transmitted by the malaria carrying Anopheles mosquitoes and Culex species play little or no role in the transmission of the disease . Very early studies elsewhere have shown that where LF transmission by Anopheles mosquitoes was interrupted through vector control alone, transmission never resumed. The control of vectors through house-spraying with residual insecticides resulted in the sustained interruption of LF by the Anopheles punctulatus group in Solomon Islands  and parts of Papua New Guinea , and cases of LF resurgence only detected in countries where Culex mosquitoes were the vectors, including Zanzibar in United Republic of Tanzania [7, 8, 29]. As suggested by Webber, vector biting rates of Anopheline mosquitoes less than 0.66 bites/man/h are unlikely to sustain the transmission of LF , and malaria control efforts targeting the Anopheles mosquito therefore have the potential to impact LF transmission in Africa [23, 38], except in areas where some species of Anopheline mosquitoes have the potential to exhibit the phenomenon of limitation [39, 40]. As such, what is the significance of areas of residual transmission on the elimination of LF? Studies elsewhere, including Mali in West Africa, have shown that the existence of areas of possible transmission did not result in resurgence of the disease [36, 37, 41]. Before China was certified free of LF in 2007, studies had shown that despite the presence of residual MF prevalence in the population, transmission was considered to have been interrupted [42, 43]. This does lead us to operate on the hypothesis that the threshold for active transmission of LF in areas where Anopheles mosquitoes exhibit facilitation is higher compared to areas where Culex mosquitoes are principal vectors. As such, these observations bring into question the importance of areas with residual infections on the elimination of LF.
This study was supported by the Filarial Programs Support Unit, through funds from DFID. We are also grateful to the study communities and participants, for accepting to take part in this study. A special thank-you to all field and laboratory workers for their participation in this study.
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- WHO. Lymphatic Filariasis: a handbook for national elimination programmes. Geneva, Switzerland: World Health Organization; 2013.Google Scholar
- Njomo DW, Mukoko DA, Nyamongo NK, Karanja J. Increasing Coverage in Mass Drug Administration for Lymphatic Filariasis Elimination in an Urban Setting: a Study of Malindi Town, Kenya. PLoS ONE. 2014;9(1), e83413.PubMed CentralView ArticlePubMedGoogle Scholar
- Weerasooriya M, Yahathugoda C, Wickramasinghe D, Gunawardena K, Dharmadasa R, Vidanapathirana K, et al. Social mobilisation, drug coverage and compliance and adverse reactions in a Mass Drug Administration (MDA) Programme for the Elimination of Lymphatic Filariasis in Sri Lanka. Filaria J. 2007;6(1):11.PubMed CentralView ArticlePubMedGoogle Scholar
- Swaminathan S, Perumal V, Adinarayanan S, Kaliannagounder K, Rengachari R, Purushothaman J. Epidemiological Assessment of Eight Rounds of Mass Drug Administration for Lymphatic Filariasis in India: Implications for Monitoring and Evaluation. PLoS Negl Trop Dis. 2012;6(11), e1926.PubMed CentralView ArticlePubMedGoogle Scholar
- Rao RU, Nagodavithana KC, Samarasekera SD, Wijegunawardana AD, Premakumara WDY, Perera SN, et al. A Comprehensive Assessment of Lymphatic Filariasis in Sri Lanka Six Years after Cessation of Mass Drug Administration. PLoS Negl Trop Dis. 2014;8(11), e3281.PubMed CentralView ArticlePubMedGoogle Scholar
- Brady M, GAELF. Seventh meeting of the Global Alliance to Eliminate Lymphatic Filariasis: reaching the vision by scaling up, scaling down, and reaching out. Parasit Vectors. 2014;7(1):46.PubMed CentralView ArticlePubMedGoogle Scholar
- Harb M, Faris R, Gad AM, Hafez ON, Ramzy RM. The resurgence of lymphatic filariasis in the Nile delta. Bull World Health Organ. 1993;71:49–54.PubMed CentralPubMedGoogle Scholar
- Sunish IP, Rajendran R, Mani TR, Munirathinam A, Tewari SC, Hiriyan J, et al. Resurgence in filarial transmission after withdrawal of mass drug administration and the relation between antigenaemia and microfilaraemia- a longitudinal study. Trop Med Int Health. 2002;7:59–69.View ArticlePubMedGoogle Scholar
- Koroma JB, Sesay S, Sonnie M, Hodges MH, Sahr F, Zhang Y, et al. Impact of Three Rounds of Mass Drug Administration on Lymphatic Filariasis in Areas Previously Treated for Onchocerciasis in Sierra Leone. PLoS Negl Trop Dis. 2013;7(6), e2273.PubMed CentralView ArticlePubMedGoogle Scholar
- Koroma J, Bangura M, Hodges M, Bah M, Zhang Y, Bockarie M. Lymphatic filariasis mapping by Immunochromatographic Test cards and baseline microfilaria survey prior to mass drug administration in Sierra Leone. Parasit Vectors. 2012;5(1):10.PubMed CentralView ArticlePubMedGoogle Scholar
- Hodges ME, Koroma JB, Sonnie M, Kennedy N, Cotter E, MacArthur C. Neglected tropical disease control in post-war Sierra Leone using the Onchocerciasis Control Programme as a platform. International Health. 2011;3(2):69–74.View ArticlePubMedGoogle Scholar
- Bennett A, Smith SJ, Yambasu S, Jambai A, Alemu W, Kabano A, et al. Household Possession and Use of Insecticide-Treated Mosquito Nets in Sierra Leone 6 Months after a National Mass-Distribution Campaign. PLoS One. 2012;7(5), e37927.PubMed CentralView ArticlePubMedGoogle Scholar
- Gerstl S, Dunkley S, Mukhtar A, Maes P, De Smet M, Baker S, et al. Long-lasting insecticide–treated net usage in eastern Sierra Leone – the success of free distribution. Trop Med Int Health. 2010;15(4):480–8.PubMedGoogle Scholar
- Dunyo SK, Nkrumah FK, Simonsen PE. Single-dose treatment of Wuchereria bancrofti infections with ivermectin and albendazole alone or in combination: evaluation of the potential for control at 12 months after treatment. Trans R Soc Trop Med Hyg. 2000;94(4):437–43.View ArticlePubMedGoogle Scholar
- Dunyo SK, Nkrumah FK, Simonsen PE. A randomized double-blind placebo-controlled field trial of ivermectin and albendazole alone and in combination for the treatment of lymphatic filariasis in Ghana. Trans R Soc Trop Med Hyg. 2000;94(2):205–11.View ArticlePubMedGoogle Scholar
- Simonsen PE, Magesa SM, Dunyo SK, Malecela-Lazaro MN, Michael E. The effect of single dose ivermectin alone or in combination with albendazole on Wuchereria bancrofti infection in primary school children in Tanzania. Trans R Soc Trop Med Hyg. 2004;98(8):462–72.Google Scholar
- Mutuku FM, King CH, Mungai P, Mbogo C, Mwangangi J, Muchiri EM, et al. Impact of insecticide-treated bed nets on malaria transmission indices on the south coast of Kenya. Malar J. 2011;10:356–6.Google Scholar
- de Souza DK, Koudou B, Kelly-Hope L, Wilson MD, Bockarie MJ, Boakye DA. Lymphatic filariasis vectors and the implications for accelerated elimination of Anopheles-transmitted filariasis in West Africa. Parasit Vectors. 2012;5:259.PubMed CentralView ArticlePubMedGoogle Scholar
- Chesnais CB, Missamou F, Pion SD, Bopda J, Louya F, Majewski AC, et al. A case study of risk factors for lymphatic filariasis in the Republic of Congo. Parasit Vectors. 2014;7:300–0.Google Scholar
- Cano J, Rebollo M, Golding N, Pullan R, Crellen T, Soler A, et al. The global distribution and transmission limits of lymphatic filariasis: past and present. Parasit Vectors. 2014;7(1):466.PubMed CentralView ArticlePubMedGoogle Scholar
- Kazura JW, Bockarie MJ. Lymphatic filariasis in Papua New Guinea: interdisciplinary research on a national health problem. Trend Parasitol. 2003;19(6):260–3.View ArticleGoogle Scholar
- Slater HC, Gambhir M, Parham PE, Michael E. Modelling Co-Infection with Malaria and Lymphatic Filariasis. PLoS Comput Biol. 2013;9(6), e1003096.PubMed CentralView ArticlePubMedGoogle Scholar
- Sodahlon YK, Dorkenoo AM, Morgah K, Nabiliou K, Agbo K, Miller R, et al. A Success Story: Togo Is Moving toward Becoming the First Sub-Saharan African Nation to Eliminate Lymphatic Filariasis through Mass Drug Administration and Countrywide Morbidity Alleviation. PLoS Negl Trop Dis. 2013;7(4), e2080.PubMed CentralView ArticlePubMedGoogle Scholar
- WHO. Monitoring and epidemiological assessment of mass drug administration in the global programme to eliminate lymphatic filariasis: a manual for national elimination programmes. In: WHO, editor. In: WHO/HTM/NTD/PCT/2011. 4th ed. Geneva: WHO; 2011. p. 1–79.Google Scholar
- de Souza DK, Sesay S, Moore MG, Ansumana R, Narh CA, Kollie K, et al. No Evidence for Lymphatic Filariasis Transmission in Big Cities Affected by Conflict Related Rural–urban Migration in Sierra Leone and Liberia. PLoS Negl Trop Dis. 2014;8(2), e2700.PubMed CentralView ArticlePubMedGoogle Scholar
- Ramzy RMR, Farid HA, Kamal IH, Ibrahim GH, Morsy ZS, et al. A polymerase chain reaction-based assay for detection of Wuchereria bancrofti in human blood and Culex pipiens. Trans R Soc Trop Med Hyg. 1997;91:156–60.View ArticlePubMedGoogle Scholar
- Takagi H, Itoh M, Kasai S, Yahathugoda TC, Weerasooriya MV, et al. Development of loop-mediated isothermal amplification method for detecting Wuchereria bancrofti DNA in human blood and vector mosquitoes. Parasitol Int. 2011;60:493–7.View ArticlePubMedGoogle Scholar
- Katholi C, Toé L, Merriweather A, Unnasch T. Determining the prevalence of Onchocerca volvulus infection in vector populations by PCR screening of pools of black flies. J Infect Dis. 1995;172:1414–7.View ArticlePubMedGoogle Scholar
- Rebollo MP, Mohammed KA, Thomas B, Ame S, Ali SM, Cano J, et al. Cessation of Mass Drug Administration for Lymphatic Filariasis in Zanzibar in 2006: Was Transmission Interrupted? PLoS Negl Trop Dis. 2015;9(3), e0003669.PubMed CentralView ArticlePubMedGoogle Scholar
- Bockarie MJ, Service MW, Barnish G, Maude GH, Greenwood BM. Malaria in a rural area of Sierra Leone. III. Vector ecology and disease transmission. Ann Trop Med Parasitol. 1994;88(3):251–62.PubMedGoogle Scholar
- Bockarie MJ, Service MW, Toure YT, Traore S, Barnish G, Greenwood BM. The ecology and behavior of the forest form of Anopheles gambiae s.s. Parassitologia. 1993;35:5–8.PubMedGoogle Scholar
- Bockarie MJ. Vector ecology and malaria transmission in southern Sierra Leone. Liverpool: UK: University of Liverpool; 1992.Google Scholar
- Bockarie MJ, Service MW, Barnish G, Toure YT. Vectorial capacity and entomologica; inoculation rates of Anopheles gambiae in a high rainfall forested area of southern Sierra Leone. Trop Med Parasitol. 1995;46:164–71.PubMedGoogle Scholar
- Schmaedick MA, Koppel AL, Pilotte N, Torres M, Williams SA, Dobson SL, et al. Molecular Xenomonitoring Using Mosquitoes to Map Lymphatic Filariasis after Mass Drug Administration in American Samoa. PLoS Negl Trop Dis. 2014;8(8), e3087.PubMed CentralView ArticlePubMedGoogle Scholar
- Farid HA, Morsy ZS, Helmy H, Ramzy RM, El Setouhy M, Weil GJ. A critical appraisal of molecular xenomonitoring as a tool for assessing progress toward elimination of Lymphatic Filariasis. Am J Trop Med Hyg. 2007;77(4):593–600.PubMed CentralPubMedGoogle Scholar
- Webber RH, Southgate BA. The maximum density of anopheline mosquitoes that can be permitted in the absence of continuing transmission of filariasis. Trans R Soc Trop Med Hyg. 1981;75:499–506.View ArticlePubMedGoogle Scholar
- Bockarie M. Can lymphatic filariasis be eradicated in Papua New Guinea? Papua New Guinea Med J. 1994;37:61–4.Google Scholar
- Kelly-Hope LA, Molyneux DH, Bockarie MJ. Can malaria vector control accelerate the interruption of lymphatic filariasis transmission in Africa; capturing a window of opportunity? Parasit Vectors. 2013;6:39.PubMed CentralView ArticlePubMedGoogle Scholar
- Amuzu H, Wilson M, Boakye D. Studies of Anopheles gambiae s.l (Diptera: Culicidae) exhibiting different vectorial capacities in lymphatic filariasis transmission in the Gomoa district, Ghana. Parasit Vectors. 2010;3(1):85.PubMed CentralView ArticlePubMedGoogle Scholar
- Boakye D, Wilson M, Appawu M, Gyapong J. Vector competence, for Wuchereria bancrofti, of the Anopheles populations in the Bongo district of Ghana. Ann Trop Med Parasitol. 2004;98(5):501–8.View ArticlePubMedGoogle Scholar
- Coulibaly YI, Dembele B, Diallo AA, Konate’ S, Dolo H, Coulibaly SY, et al. The impact of six annual rounds of mass drug administration on Wuchereria bancrofti infections in humans and in mosquitoes in Mali. Am J Trop Med Hyg. 2015. doi:10.4269/ajtmh.14-0516.Google Scholar
- De-jian S, Xu-li D, Ji-hui D. The history of the elimination of lymphatic filariasis in China. Infectious Diseases of Poverty. 2013;2(1):30.PubMed CentralView ArticlePubMedGoogle Scholar
- Shi ZJ. Study on the transmission threshold of filariasis. Chin J Parasitol Parasit Dis. 1994;12(1):1–6.Google Scholar