Mosquitos are the most lethal animal species to humans. Annually, diseases transmitted by mosquitoes kill more than one million people and infect up to 700 million. These diseases include malaria, dengue, Zika and Japanese encephalitis. Malaria causes over half of these deaths. Now, climate change is driving mosquitos into areas previously unaffected. In Europe, over the past decade, locally transmitted dengue outbreaks have increased. Burnet collaborates with teams worldwide to reduce the burden of mosquito-borne diseases and protect people at risk.
Malaria is the deadliest mosquito-borne disease. In 2023, there were an estimated 263 million malaria cases and 597,000 deaths in 83 countries. That amounts to approximately 68 deaths per hour. Ninety-five per cent of malaria-related deaths were in Africa. Seventy-six of these deaths were children under 5.
Malaria is caused when female Anopheles mosquitoes spread the Plasmodium parasite between humans.
The most significant Plasmodium species are:
After decades of public health effort, malaria was officially eliminated from Australia in 1981. However, reintroduction remains a risk.
Malaria is endemic in approximately 85 countries, including the Americas, Africa, Southeast Asia, Western Pacific and the Eastern Mediterranean region.
Malaria challenges include:
There's also a lack of sensitive tools for:
Australia’s generation X face the highest risk of death from methamphetamine-related causes among all age groups, according to a new Burnet Institute study.
We research other diseases carried by mosquitoes, including:
Climate change enables mosquitoes and the diseases they carry to spread into new regions. If health systems in such regions have limited resources, mosquito-borne diseases could become established there.
We combine laboratory discovery with public health implementation and expertise in international development.
We also work in close partnership with communities and health systems across Africa, South-East Asia and the Pacific.
Our work aligns with the World Health Organization’s Global Technical Strategy for Malaria 2016–2030, including:
We develop and evaluate new diagnostic technologies to support earlier, more accurate detection of malaria, dengue, Zika and Japanese encephalitis. This includes tools for improved case management, genomic surveillance and resistance monitoring. For example, we’re investigating the integration of more sensitive malaria detection techniques into national surveillance systems.
We focus on understanding immune responses to Plasmodium falciparum and P. vivax to inform effective vaccine design.
Our laboratory research advances the development and evaluation of leading malaria vaccine candidates. For example, we’re researching immune responses generated by malaria vaccination in young children across Africa.
We are developing new antimalarial drugs and tracking and preventing the spread of drug resistance, especially in the Asia-Pacific region.
We aim to accelerate deployment of new treatments. For example, we are researching new antimalarial drugs to overcome Plasmodium drug resistance.
Burnet conducts implementation research to improve healthcare services and malaria prevention.
We support modelling and evaluation of interventions for malaria across endemic regions. For example, in the Indo-Pacific region, our ADVANCE project aims to improve access to new malaria diagnostic tools.
To achieve malaria elimination goals, we research mosquito behaviour and integrated control strategies.
To control the spread of viruses such as dengue, Zika and chikungunya, we study and evaluate use of the Wolbachia bacterium.
Burnet is at the forefront of research into mosquito-borne diseases. Our work influences global health policies, clinical guidelines and vaccine development.
In Papua New Guinea and the Greater Mekong region, we demonstrated how community-led molecular and serological surveillance can be integrated into national systems.
In the Greater Mekong region and Papua New Guinea, we developed mobile app-based advanced malaria surveillance tools to improve case detection, surveillance and use of data for informed decision-making.
We study targets from malaria parasites around the world. By knowing how much they differ, we can create a ‘guide’ to develop vaccines that work in multiple regions and against different strains.
We also delivered critical insights into the performance of the RTS,S malaria vaccine among young children in a malaria-endemic area.
We identified protective antibody targets and predicted antigen combinations for highly effective vaccines. This work directly informed international vaccine development.
In Papua New Guinea, we discovered a local emergence of artemisinin resistance mutations. This led to the World Health Organization (WHO) changing its definition of artemisinin resistance, increasing the accuracy of resistance surveillance.
Burnet led the first trial demonstrating how personal mosquito repellent can prevent malaria. The WHO used this evidence to inform their regional policy. Together with partners in PNG, we are evaluating new vector control tools to target outdoor transmission.
We provided the first evidence that artemisinin drugs are safe to use in early pregnancy. As a result, the WHO revised its treatment guidelines. Our research linked malaria to 200,000 global stillbirths per year and showed how preventive treatment reduces the risk. Informed by our work, the WHO updated its policy in Asia.
Burnet, WEHI and the Australian Government have teamed up to work on malaria elimination with countries across the Pacific and South-East Asia.
PLoS Biology
Zahra Razook, Madeline G. Dans, Somya Mehra, Molly Parkyn Schneider, Thorey K. Jonsdottir, Mikha Gabriela, Alyssa E. Barry, Brendan S. Crabb, Paul R. Gilson, Madeline G. Dans
Nature Communications
Zahra Razook, Madeline G. Dans, Coralie Boulet, Somya Mehra, Dawson B. Ling, Thorey K. Jonsdottir, Coralie Boulet, Madeline G. Dans, Somya Mehra, Zahra Razook
We seek to quantify the impact of malaria control measures including the potential elimination on malaria immunity within communities.
We aim to determine how malaria immunity impacts on the transmission of malaria and how immunity influences malaria control interventions.