Large-scale intermittent larviciding intervention and associations with key malaria epidemiological parameters in Tanga Region, Tanzania
(2025) 24:350
Kailembo et al. Malaria Journal
https://doi.org/10.1186/s12936-025-05548-7
Malaria Journal
Open Access
RESEARCH
Large‑scale intermittent larviciding
intervention and associations with key malaria
epidemiological parameters in Tanga Region,
Tanzania
Denis Kailembo1,2*, Tegemeo Gavana1,2,3, Elizabeth Kasagama1,2, Jubilate Bernard4, Fabrizio Molteni1,2,
Noela Kisoka1,2, Best Yoram5, Stella Kajange5, Samwel Lazaro4, Charles Dismas4, Amanda Ross1,2,
Prosper Chaki3 and Christian Lengeler1,2
Abstract
Background Malaria remains one of the major public health problems both globally and in Tanzania. In addition
to existing malaria control interventions, the country plans to introduce larviciding in its efforts towards malaria
control and elimination. To guide a possible national upscaling of the intervention, a pilot larviciding study using
biolarvicides produced in-country was implemented and evaluated to generate a body of evidence on operations
and the impact of the intervention. The current manuscript reports on the association between larviciding and three
major malaria epidemiological parameters.
Methods Larviciding was conducted in three councils in Tanga Region in the North-East of the country and covered a population of over 1.1 million. The councils represented different malaria risk strata: high, moderate, and low.
Larviciding was conducted between June 2022 and April 2024 through a community-based approach using existing
local government structures. Larviciding was applied intermittently in the intervention councils to all identified breeding habitats for three rounds per year, based on the local rainfall seasons. Both Bacillus thuringiensis var. israelensis
and Bacillus sphaericus were used and each round comprised of 8 consecutive weeks of biolarvicide application. Epidemiological data, including malaria incidence, laboratory malaria test positivity rate and antenatal malaria test positivity rate, were collected from routine health facility data. Each intervention council was paired with multiple control
councils based on malaria risk and rainfall patterns, allowing a controlled before-after study design. The association
between larviciding and malaria incidence was assessed using negative binomial regression while logistic regression
was used for the other epidemiological outcomes.
Results The intervention did not have a significant association with the incidence of reported clinical malaria
among all age-groups. The estimated incidence rate ratio (IRR) was 1.16 (95% CI 0.98; 1.37) in the high, 0.86 (95% CI
0.72; 1.02) in the moderate, and 0.96 (95% CI 0.76; 1.22) in the low stratum. Similar results were observed across other
epidemiological parameters. There was a slight tendency for estimates in the moderate and low strata to be
in the direction of a reduction.
*Correspondence:
Denis Kailembo
Full list of author information is available at the end of the article
© The Author(s) 2025. Open Access This article is licensed under a Creative Commons Attribution-NonCommercial-NoDerivatives 4.0
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Kailembo et al. Malaria Journal
(2025) 24:350
Page 2 of 13
Conclusion Under the current design of intermittent larviciding application, there was no strong evidence
of an association between larviciding and malaria epidemiological indicators. More studies considering continuous
year-round implementation and randomizing a large number of clusters could generate further evidence on the contribution of larviciding to malaria control in similar transmission settings.
Keywords Malaria, Larviciding, Bacillus thuringiensis var. israelensis, Bacillus sphaericus, Malaria control, Tanzania
Mainland
Background
Malaria remains one of the major global public health
problems. The World Health Organization (WHO) estimated that there were 263 million malaria cases worldwide in 2023 [1], of which around 246 million (94%) were
from the WHO African Region. In Tanzania, malaria is a
major cause of morbidity and mortality, with over three
million clinical cases reported through routine health
facilities in 2024 [2].
Insecticide-treated mosquito nets (ITNs), and indoor
residual spraying (IRS) have been shown to have a major
impact in reducing the burden of malaria [3, 4]. Following large advances achieved by scaling up interventions
between 2000 and 2015, reductions in the malaria burden
have stagnated over the past decade [1]. In Tanzania, the
malaria prevalence among children under 5 years of age
remained relatively unchanged between 2017 and 2022 at
7.3% [5] and 8.1% [6], respectively. Emerging resistance to
insecticides used in ITNs and IRS has been documented
[7–14], as well as concerns about the durability of standard ITNs [15–18]. Moreover, changes in vector behavior from indoor to outdoor biting and resting have also
been reported [19–22]. These challenges underscore the
urgent need for additional preventive measures.
Larval Source Management (LSM) is one of the supplementary malaria control measures recommended by
the WHO. It is defined as the management of potential
mosquito breeding habitats to prevent the maturation
of mosquito larvae to the adult stage [23]. LSM can be
implemented through environmental management (i.e.
habitat modification and habitat manipulation), biological control, and larviciding. To date, LSM implementation in sub-Saharan Africa (SSA) has been primarily
through larviciding. The WHO does not currently recommend the implementation of larviciding in all areas,
but only where breeding habitats are few, fixed and findable [23].
The impact of LSM on malaria control through environmental management and larviciding, conducted
either alone or in combination, was assessed in a 2013
Cochrane Systematic Review, whereby the findings
showed mixed results [24]. A more recent Cochrane
Systematic Review, in 2019 which included four studies
assessed only the impact of larviciding on malaria control
and also found mixed results [25]. While one study in SriLanka used insect growth regulators, the studies in Tanzania, Kenya and The Gambia used microbial larv (...truncated)