The efficacy of attractive targeted sugar baits in reducing malaria vector abundance in low-endemicity settings of northwest Mali.
Anopheles gambiae
ATSB
Bait station
Entomological inoculation rate (EIR)
Malaria
Mali
Journal
Malaria journal
ISSN: 1475-2875
Titre abrégé: Malar J
Pays: England
ID NLM: 101139802
Informations de publication
Date de publication:
23 Oct 2024
23 Oct 2024
Historique:
received:
05
01
2024
accepted:
28
08
2024
medline:
24
10
2024
pubmed:
24
10
2024
entrez:
24
10
2024
Statut:
epublish
Résumé
Attractive targeted sugar baits (ATSBs) have the potential to significantly reduce infective female Anopheles mosquitoes in arid areas, such as in Northern Mali. Malaria is epidemic in the north due to the limited viability of Anopheles species in the desert climate. The goal of this study was to determine of the effect of ATSB on the number of older female An. gambiae and on the number of sporozoite-positive females in villages in northern Mali. Villages were located in the north of Mali. In this study, 5677 ATSB stations were deployed, two on each home, in ten villages during late July and early August 2019. Ten villages served as controls. After a pre-treatment monitoring period in July, An. gambiae populations were monitored again from August to December using CDC-UV light traps, pyrethrum spray catches (PSC), and human landing catches (HLC). Mosquitoes were dissected to estimate their age, while ELISA detected sporozoite positivity. The monthly entomological inoculation rates (EIRs) were calculated for HLC indoors and outdoors. Data from villages were compared using t-tests, while bait station weighted density versus amount of collected females was checked with a Pearson's correlation. A total of 2703 female An. gambiae were caught from treated villages, 4582 from control villages, a 41.0% difference. Dissection of 1759 females showed that ATSB significantly reduced the number of older females. The proportion of older females in treated villages was 0.93% compared to 9.4% in control villages. ELISA analysis of 7285 females showed that bait stations reduced the number of sporozoite-positive females. The infective females in treated villages was 0.30% compared to 2.73% in the controls. The greater the density of bait stations deployed, the fewer the older, infective females (P < 0.05). EIRs were low in control villages except in months when An. gambiae populations were high. EIRs in ATSB placement villages remained zero. Significant reductions (P < 0.0001) in An. gambiae males were observed. Bait stations reduced all measures of vector populations in this study. In a low-transmission setting, ATSB has the potential to greatly reduce malaria.
Sections du résumé
BACKGROUND
BACKGROUND
Attractive targeted sugar baits (ATSBs) have the potential to significantly reduce infective female Anopheles mosquitoes in arid areas, such as in Northern Mali. Malaria is epidemic in the north due to the limited viability of Anopheles species in the desert climate. The goal of this study was to determine of the effect of ATSB on the number of older female An. gambiae and on the number of sporozoite-positive females in villages in northern Mali.
METHODS
METHODS
Villages were located in the north of Mali. In this study, 5677 ATSB stations were deployed, two on each home, in ten villages during late July and early August 2019. Ten villages served as controls. After a pre-treatment monitoring period in July, An. gambiae populations were monitored again from August to December using CDC-UV light traps, pyrethrum spray catches (PSC), and human landing catches (HLC). Mosquitoes were dissected to estimate their age, while ELISA detected sporozoite positivity. The monthly entomological inoculation rates (EIRs) were calculated for HLC indoors and outdoors. Data from villages were compared using t-tests, while bait station weighted density versus amount of collected females was checked with a Pearson's correlation.
RESULTS
RESULTS
A total of 2703 female An. gambiae were caught from treated villages, 4582 from control villages, a 41.0% difference. Dissection of 1759 females showed that ATSB significantly reduced the number of older females. The proportion of older females in treated villages was 0.93% compared to 9.4% in control villages. ELISA analysis of 7285 females showed that bait stations reduced the number of sporozoite-positive females. The infective females in treated villages was 0.30% compared to 2.73% in the controls. The greater the density of bait stations deployed, the fewer the older, infective females (P < 0.05). EIRs were low in control villages except in months when An. gambiae populations were high. EIRs in ATSB placement villages remained zero. Significant reductions (P < 0.0001) in An. gambiae males were observed.
CONCLUSIONS
CONCLUSIONS
Bait stations reduced all measures of vector populations in this study. In a low-transmission setting, ATSB has the potential to greatly reduce malaria.
Identifiants
pubmed: 39443969
doi: 10.1186/s12936-024-05098-4
pii: 10.1186/s12936-024-05098-4
doi:
Substances chimiques
Sugars
0
Types de publication
Journal Article
Langues
eng
Sous-ensembles de citation
IM
Pagination
319Informations de copyright
© 2024. The Author(s).
Références
WHO. World Malaria report 2020: 20 years of global progress and challenges. Geneva: World Health Organization; 2020. p. 2020.
Traore MM, Junnila A, Traore SF, Doumbia S, Revay EE, Kravchenko VD, et al. Large-scale field trial of attractive toxic sugar baits (ATSB) for the control of malaria vector mosquitoes in Mali, West Africa. Malar J. 2020;19:72.
doi: 10.1186/s12936-020-3132-0
pubmed: 32059671
pmcid: 7023716
Müller GC, Junnila A, Schlein Y. Effective control of adult Culex pipiens by spraying an attractive toxic sugar bait solution in the vegetation near larval habitats. J Med Entomol. 2010;47:63–6.
doi: 10.1093/jmedent/47.1.63
pubmed: 20180309
Müller GC, Schlein Y. Efficacy of toxic sugar baits against adult cistern-dwelling Anopheles claviger. Trans R Soc Trop Med Hyg. 2008;102:480–4.
doi: 10.1016/j.trstmh.2008.01.008
pubmed: 18387642
Müller GC, Kravchenko VD, Schlein Y. Decline of Anopheles sergentii and Aedes caspius populations following presentation of attractive toxic (Spinosad) sugar bait stations in an oasis. J Am Mosq Control Assoc. 2008;24:147–9.
doi: 10.2987/8756-971X(2008)24[147:DOASAA]2.0.CO;2
pubmed: 18437830
Diarra RA, Traore MM, Junnila A, Traore SF, Doumbia S, Revay EE, et al. Testing configurations of attractive toxic sugar bait (ATSB) stations in Mali, West Africa, for improving the control of malaria parasite transmission by vector mosquitoes and minimizing their effect on non-target insects. Malar J. 2021;20:184.
doi: 10.1186/s12936-021-03704-3
pubmed: 33853632
pmcid: 8048058
Lehmann T, Dao A, Yaro AS, Diallo M, Timbiné S, Huestis DL, et al. Seasonal variation in spatial distributions of Anopheles gambiae in a Sahelian village: evidence for aestivation. J Med Entomol. 2014;51:27–38.
doi: 10.1603/ME13094
pubmed: 24605449
United States Environmental Protection Agency (EPA). Product performance test guidelines OPPTS 810.3700: insect repellents to be applied to human skin. 2010; 712-C-10-00.
Tambwe MM, Kibondo UA, Odufuwa OG, Moore J, Mpelepele A, Mashauri R, Saddler A, Moore SJ. Human landing catches provide a useful measure of protective efficacy for the evaluation of volatile pyrethroid spatial repellents. Parasit Vectors. 2023;16:90.
doi: 10.1186/s13071-023-05685-5
pubmed: 36882842
pmcid: 9993701
WHO. Manual on practical entomology. Parts 1 and 2. Methods and techniques No. 13. Geneva: World Health Organization; 1975.
Detinova TS, Bertram DS, WHO. Age-grouping methods in Diptera of medical importance, with special reference to some vectors of malaria. Monograph Series 47. Geneva: World Health Organization; 1962.
doi: 10.2307/3275215
Beier MS, Schwartz IK, Beier JC, Perkins PV, Onyango F, Koros JK, et al. Identification of malaria species by ELISA in sporozoite and oocyst infected Anopheles from western Kenya. Am J Trop Med Hyg. 1988;39:323–7.
doi: 10.4269/ajtmh.1988.39.323
pubmed: 3056055
Beier JC. Vector incrimination and entomological inoculation rates. In: Doolan DL, editor. Malaria methods and protocols. Totowa: Humana Press; 2002.
Schlein Y, Müller GC. An approach to mosquito control: using the dominant attraction of flowering Tamarix jordanis trees against Culex pipiens. J Med Entomol. 2014;29(45):384–90.
Beier JC, Müller GC, Gu W, Arheart KL, Schlein Y. Attractive toxic sugar bait (ATSB) methods decimate populations of Anopheles malaria vectors in arid environments regardless of the local availability of favoured sugar-source blossoms. Malar J. 2012;11:31.
doi: 10.1186/1475-2875-11-31
pubmed: 22297155
pmcid: 3293779
Müller GC, Beier JC, Traore SF, Toure MB, Traore MM, Bah S, Doumbia S, Schlein Y. Field experiments of Anopheles gambiae attraction to local fruits/seedpods and flowering plants in Mali to optimize strategies for malaria vector control in Africa using attractive toxic sugar bait methods. Malar J. 2010;9:262.
doi: 10.1186/1475-2875-9-262
pubmed: 20854666
pmcid: 2949744
Gillies MT. The duration of the gonotrophic cycle in Anopheles gambiae and Anopheles funestus, with a note on the efficiency of hand catching. East Afr Med J. 1953;30:129–35.
pubmed: 13060242
malERA Consultative Group on Vector Control. A research agenda for malaria eradication: vector control. PLoS Med. 2011;8: e1000401.
doi: 10.1371/journal.pmed.1000401
Hemingway J, Shretta R, Wells TN, Bell D, Djimdé AA, Achee N, et al. Tools and strategies for malaria control and elimination: what do we need to achieve a grand convergence in malaria? PLoS Biol. 2016;14: e1002380.
doi: 10.1371/journal.pbio.1002380
pubmed: 26934361
pmcid: 4774904
Greenwood B. New tools for malaria control—using them wisely. J Infect. 2017;74(Suppl 1):S23–6.
doi: 10.1016/S0163-4453(17)30187-1
pubmed: 28646958