BBC News 9 Sep 09;
An emerging new form of malaria poses a deadly threat to humans, research has shown.
It had been thought the parasite Plasmodium knowlesi infected only monkeys.
But it has recently been found to be widespread in humans in Malaysia, and the latest study confirms that it can kill if not treated quickly.
The work, by an international team, appears in the journal Clinical Infectious Diseases.
Although the new form of the disease has so far been concentrated in South East Asia, the researchers warn that tourism to the region could soon see cases appearing in Western countries too.
Malaria kills more than a million people each year.
It is caused by malaria parasites, which are injected into the bloodstream by infected mosquitoes.
Of the four species of malaria parasite that often cause disease in humans, P. falciparum, found most commonly in Africa, is the most deadly.
Another parasite, P. malariae, found in tropical and sub-tropical regions across the globe, has symptoms that are usually less serious.
P. knowlesi had been thought only to infect monkeys, in particular long-tailed and pig-tailed macaques found in the rainforests of South East Asia.
But following work by a team at the University Malaysia Sarawak it has now been recognised as a significant cause of disease in humans.
The latest study shows that P. knowlesi can easily be confused with P. malariae under the microscope.
Speedy reproduction
However, unlike its cousin, P. knowlesi has the ability to reproduce every 24 hours in the blood - meaning infection is potentially deadly.
Researcher Professor Balbir Singh said this meant early diagnosis and treatment were crucial.
The researchers carried out tests on over 150 patients admitted to hospital in Sarawak, Malaysian Borneo, between July 2006 and January 2008 with malaria infection.
They found that P. knowlesi accounted for more than two-thirds of the infections, resulting in a wide spectrum of disease.
Most cases of infection were uncomplicated and easily treated with drugs, including chloroquine and primaquine.
However, around one in ten patients had developed complications, such as breathing difficulties and kidney problems, and two died.
Although the fatality rate was just under 2%, that made P. knowlesi as deadly as P. falciparum malaria.
And the researchers stress it is hard to determine an accurate fatality rate given the small number of cases so far studied.
Low platelet count
All of the P. knowlesi patients had a low blood platelet count, significantly lower than that usually found for other types of malaria.
However, even though blood platelets are essential for blood clotting, no cases of excessive bleeding or problems with clotting were identified.
The researchers believe the low blood platelet count could be used as a potential way to diagnose P. knowlesi infections.
Professor Singh said: "The increase in tourism in South East Asia may mean that more cases are detected in the future, including in Western countries.
"Clinicians assessing a patient who has visited an area with known or possible P. knowlesi transmission should be aware of the diagnosis, clinical manifestations, and rapid and potentially serious course of P. knowlesi malaria."
Monkey malaria kills humans
ScienceAlert 15 Sep 09;
Researchers in Malaysia have identified key laboratory and clinical features of an emerging new form of malaria infection. The research, funded by the Wellcome Trust, confirms the potentially deadly nature of the disease.
Malaria kills more than a million people each year. It is caused by malaria parasites, which are injected into the bloodstream by infected mosquitoes. Of the four species of malaria that commonly cause disease in humans, Plasmodium falciparum, found most commonly in Africa, is the most deadly. P. malariae, found in tropical and sub-tropical regions across the globe, has symptoms that are usually less serious.
Recently, researchers at the University Malaysia Sarawak, led by Professors Balbir Singh and Janet Cox-Singh, showed that P. knowlesi, a malaria parasite previously thought to mainly infect only monkeys – in particular long-tailed and pig-tailed macaques found in the rainforests of Southeast Asia – was widespread amongst humans in Malaysia. Subsequent reports in neighbouring Southeast Asian countries have led to the recognition of P. knowlesi as the fifth cause of malaria in humans.
Now, in a study published in the journal Clinical Infectious Diseases, Professors Singh and Cox-Singh, together with colleagues from University Malaysia Sarawak, Kapit Hospital and the University of Western Australia, have published the first detailed prospective study of the clinical and laboratory features of human P. knowlesi infections.
"P. knowlesi malaria can easily be confused with P. malariae since these two parasites look similar by microscopy, but the latter causes a benign form of malaria," says Professor Singh. "In fact, because the P. knowlesi parasites reproduce every twenty four hours in the blood, the disease can be potentially fatal, so early diagnosis and appropriate treatment is essential. Understanding the most common features of the disease will be important in helping make this diagnosis and in planning appropriate clinical management."
The researchers initially recruited over 150 patients admitted to Kapit Hospital in Sarawak, Malaysian Borneo, between July 2006 and January 2008 who had tested positive with a blood film slide for Plasmodium species. Using molecular detection methods, P. knowlesi was found to be by far the most common infection amongst these patients, accounting for over two-thirds of all cases.
As with other types of malaria in humans, P. knowlesi infections resulted in a wide spectrum of disease. Most cases of infection were uncomplicated and easily treated with chloroquine and primaquine, two commonly used anti-malarial drugs. However, around one in ten patients had developed complications and two died. Complications included breathing difficulties and kidney problems (including kidney failure in a small number of cases), which are also common in severe P. falciparum cases. Although the researchers saw a case fatality rate of just under 2 per cent, which makes P. knowlesi malaria as deadly as P. falciparum malaria, they stress that an accurate fatality rate is hard to determine given the relatively small number of cases studied so far.
All of the P. knowlesi patients – including those with uncomplicated malaria – had a low blood platelet count. In other human forms of malaria, this would only be expected in less than eight out of ten cases. In addition, the P. knowlesi platelet counts tended to be significantly lower than for other malarias. However, even though blood platelets are essential for blood clotting, no cases of excessive bleeding or problems with clotting were identified. The researchers believe the low blood platelet count could be used as a potential feature for diagnosis of P. knowlesi infections.
Recently, there have been cases of European travellers to Malaysia and an American traveller to the Philippines being admitted into hospital with knowlesi malaria following their return home.
"The increase in tourism in Southeast Asia may mean that more cases are detected in the future, including in Western countries," says Professor Singh. "Clinicians assessing a patient who has visited an area with known or possible P. knowlesi transmission should be aware of the diagnosis, clinical manifestations, and rapid and potentially serious course of P. knowlesi malaria."
