Every two minutes a child dies from malaria. Imagine the devastating impact this has on families and their communities.
Malaria is an acute febrile illness caused by different species of parasite: Plasmodium falciparum, P. vivax, P. ovale, P. malariae and P. knowlesi. Falciparum causes the majority of malaria disease globally, but P. vivax is a second important cause of malaria and causes a high burden of disease in the Asia-Pacific region.
These parasites are transmitted to humans via the bites of infected mosquitoes, which cause malaria. They multiply in the liver, then infect the red blood cells, and if not promptly treated, may lead to death.
The World Health Organization (WHO) reported 229 million cases of malaria worldwide in 2019, which resulted in 403,000 deaths, mostly in sub-Saharan Africa. The incidence rate of malaria declined globally between 2010 and 2018, from 71 to 57 cases per 1000 population at risk. But between 2015 and 2019 it declined by less than 2%, indicating a slowing of the rate of decline.
The number of deaths has fallen from 736,000 in 2000 to 409,000 in 2019.
Pregnancy reduces a women’s immunity to malaria, and the disease can interfere with the growth of the fetus, increasing the risk of premature birth and low birth weight – a leading cause of child mortality.
Discover more about Burnet’s malaria work in Episode 8 of our How Science Matters podcast.
Burnet Institute is committed to making a major contribution in efforts to eliminate malaria as a public health threat, particularly in the Asia-Pacific region. We work with partners in Australia and internationally, especially in malaria-endemic regions in the
Pacific, Southeast Asia and East Africa (including Papua New Guinea, Myanmar, Vietnam, Lao PDR, Kenya, and Cambodia). We also collaborate with industry partners in development of vaccines, diagnostics and therapeutics.
Burnet’s latest discoveries and innovative approaches
Discovering new insights into how drug resistance may emerge in populations and how to better quantify and monitor its spread.
Identified new antimalarial compounds with potential for development into drugs.
Identified immune responses that protect against malaria and new approaches for vaccine development.
Developing new low-cost diagnostic tests to guide the treatment of malaria.
Developing novel tools to enhance surveillance and tracking of malaria in populations.
Established the real-world effectiveness of repellant distribution in large-scale disease prevention programs in Myanmar and demonstrated that it can prevent a third of new malaria infections.
In affected communities created strategies to address gaps in health services and coverage to improve diagnosis, treatment, and prevention.
Drug resistance
According to the WHO, antimalarial drug resistance is a major concern for the global effort to control malaria.
Resistance to Artemisinin - a group of drugs used to treat malaria caused by the P.falciparum parasite - has been confirmed in countries including Cambodia, Lao People’s Democratic Republic, and Vietnam. The presence of the molecular markers of Artemisinin resistance has been reported in Bangladesh, India, Myanmar and Thailand.
Burnet’s Eliminate Malaria program:
Burnet’s Key Strategies:
The landmark 1st Malaria World Congress 2018 (MWC2018) raised awareness internationally about the huge global challenges to eliminate this devastating disease. Find out more. Burnet’s malaria researchers and Congress Founder, Professor Brendan Crabb AC played a key role.
Antibody engineering to study responses mediating protective immunity
APPRISE - Centre for Research Excellence
Broadly neutralising anti-HIV antibodies and Fc Receptor function
Clinical studies on malaria
Decision science using Optima
Developing new antimalarial drugs that block protein trafficking
Developing vaccines against malaria
Discovering the mechanisms and targets of immunity against malaria
Evaluating a highly sensitive rapid malaria diagnostic in PNG
Evaluation of Malaria Case-Based Reporting using a mobile phone application in Myanmar
Evidence and action for malaria elimination in Myanmar
Healthy Mothers, Healthy Babies
HMHB - Health Services for Postnatal and Infancy Care
HMHB: The impact of nutrition, malaria and STIs on pregnant women and infants
Host and parasite factors that predict Artemisinin Resistance reservoirs
Host red blood cell modification sustains the virulence of malaria parasites
Immunity to malaria and infectious diseases during pregnancy
Immunity, drug efficacy and spread of antimalarial drug resistance
Impact of declining transmission on immunity and risk of malaria rebound
Iron deficiency anaemia and adverse birth outcomes in a malaria-endemic region of Papua New Guinea
Major advances in understanding malaria immunity and biology
Mechanism of antimalarial drug action
NATNAT: Newly Adapted Tools and Network Against Mosquito Borne Disease Transmission
Optima Malaria Modelling
Optimal community-delivered malaria elimination models for the Greater Mekong Sub-region
PAVE PNG - PArtnership for Vivax Elimination
Serological surveillance to identify mosquito exposure and malaria transmission
Stellabody® Technology in Infectious Disease – COVID-19 and beyond
STRIVE PNG: Stronger Surveillance and Systems Support for Rapid Identification and Containment of Resurgent or Resistant Vector-Borne Pathogens in Papua New Guinea
Vaccines against Plasmodium vivax and P. falciparum malaria
Past Projects
New treatments for malaria
Understanding the acquisition and maintenance of antibodies against malaria
This website was developed with the generous support of a donor.
Burnet Institute (Australia) is located on the traditional land of the Boon Wurrung people and we offer our respects to their Elders past and present. We recognise and respect the continuation of cultural, spiritual and educational practices of Aboriginal and Torres Strait Islander peoples of this land.
Oops!
It looks like something may have gone wrong, and some of the resources required to load the page may not have loaded correctly.