Malaria Journal

, 15:24 | Cite as

Mind the gap: residual malaria transmission, veterinary endectocides and livestock as targets for malaria vector control

Open Access
Commentary

Keywords

Ivermectin Endectocides Vector control Residual transmission Livestock Zoophilic vectors Malaria elimination 

Abbreviations

LLINs

long-lasting insecticide-treated nets

IRS

indoor residual spraying

The work of Pooda et al. published in Malaria Journal [1] provides encouraging evidence of the potential use of systemic insecticides in cattle as a complementary means to further reduce residual malaria transmission that persists despite high coverage of current front-line vector measures, namely long-lasting insecticidal nets (LLINs) and indoor residual sprays (IRS).

LLINs and IRS interventions are responsible for most of the remarkable reductions in malaria burden achieved in this century [2], but even more ambitious new vector control measures will be required to achieve elimination of transmission from most endemic areas in the years ahead [3, 4, 5]. This is because LLINs and IRS leave two obvious spatial and temporal gaps wherever vector mosquitoes attack people outdoors, especially in the evenings and mornings, or rest outdoors before and after feeding [3, 4, 5]. There is, however, a third gap that does not usually receive as much attention, specifically their failure to kill mosquitoes that feed on animals rather than humans.

Zoophagic vectors that feed predominantly on animals can sustain malaria transmission even if they only bite humans infrequently [6]. Even with near-complete coverage of human sleeping spaces and houses, LLINs and IRS cannot be reasonably expected to have any meaningful impact upon the density or longevity of zoophagic vector populations, because they achieve no insecticidal coverage of the animals that constitute their main source of protein [4, 6].

Fortunately, by far the most common source of blood for most zoophagic malaria vectors are domesticated livestock, cattle in particular [7], so it is also possible to control the malaria transmission they mediate through veterinary applications of insecticides [8], the most exciting of which may be the systemic insecticides which the mosquito actually ingests along with its blood meal. Fritz et al. first described increased mortality of Anopheles gambiae feeding on ivermectin-treated cattle and suggested a potential role of this strategy for integrated vector management [9]. These findings have since been extended to Anopheles culicifacies and Anopheles stephensi, the main malaria vectors of Pakistan [10], and more recently to an important African vector of residual transmission, Anopheles arabiensis [11].

This latest report by Pooda et al. [1] now demonstrates similar increased mortality and reduced fertility of Anopheles coluzzii, a widely distributed vector species which maintains robust malaria transmission all across west and central Africa [12]. Interestingly, the lethal effect of ivermectin was seen even when the colony used had high prevalence of the kdr mutation which contributes to pyrethroid resistance in many parts of Africa.

Although the evidence base is growing fast, the full potential of ivermectin for malaria vector and transmission control remains to be established, but most discourse thus far has focused on medical delivery to human beings [13]. However, the alternative strategy of veterinary delivery to livestock has several advantages:
  • Long-lasting injectable veterinary formulations of ivermectin already exist that can dramatically increase the effectiveness of this approach, by not only targeting a more important blood source for vector populations than humans, but also by achieving far longer duration of efficacy than is possible with the oral formulations available for human pharmaceutical delivery.

  • A much greater diversity of different endectocides are available for cattle and other livestock, which offers an opportunity to combine drugs with different mechanisms of action, especially if ivermectin is to be used for mass drug administration to humans.

  • Integrating an endectocide into traditional zooprophylaxis strategies [14] removes potential risks of accidentally increasing malaria transmission by increasing vector survival and reproduction [15], because mosquitoes attracted to feeding on animals could be killed rather than merely diverted away from humans.

  • Endectocides can contribute to an overall One Health strategy by simultaneously improving livestock and human health. Nonzoonotic livestock parasites pose an important burden on human health by reducing economic output and nutrient availability. In addition to preventing malaria transmission, broadening the use of veterinary endectocides also offers an excellent opportunity to alleviate poverty and malnutrition by reducing the burden of livestock parasites on the health and economic resilience of their human owners [16].

Plasmodium falciparum and Plasmodium vivax are both strict anthroponoses, so it is understandable that ivermectin mass drug administration for malaria control and elimination is usually viewed primarily as an intervention for human populations. However, the use of veterinary antiparasitic drugs with insecticidal proprieties in domesticated livestock could perhaps achieve greater impact in many settings where persisting transmission is mediated by zoophagic vectors, and contribute to human health in previously unforeseen ways.

Notes

Competing interests

Both authors declare that they have no competing interests.

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Copyright information

© Chaccour and Killeen. 2016

Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.

Authors and Affiliations

  1. 1.Department of Internal MedicineClinica Universidad de NavarraPamplonaSpain
  2. 2.ISGlobal, Barcelona Ctr. Int. Health Res. (CRESIB), Hospital ClínicUniversitat de BarcelonaBarcelonaSpain
  3. 3.Instituto de Salud TropicalUniversidad de NavarraPamplonaSpain
  4. 4.Ifakara Health InstituteEnvironmental Health and Ecological Sciences Thematic GroupMorogoroUnited Republic of Tanzania
  5. 5.Department of Vector BiologyLiverpool School of Tropical MedicineLiverpoolUK

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