The Mosquitos-Men Foe: the story of Malaria
Mayleen Lee
To many humans,
Mosquitos seem harmless in any possible way: tiny, soft, and squishable.
The reality,
however, is unfortunately very ironic.
Mosquitoes have
caused more human suffering than any other organism in the human history – more
than one million people die from mosquito-transmitted
diseases worldwide every year since ancient time.
Malaria perfect
demonstrates this formidable foe between mosquitos and men. Malaria, caused by infection from Plasmodium parasites, is transmitted to
people through the bites of infected mosquitoes. The stings, particularly from Anopheles mosquitoes, would normally lead
to seemly mild symptoms such as fever and headache, making them difficult to be
recognized as Malaria. According to the World Health Organization (WHO),
untreated Malaria can progress in 24 hours and lead to death. This makes Malaria the deadliest infectious
disease in history, taking 1.2 million lives per year.
The medical
world has put lots of efforts into creating effective vaccine for Malaria. It turns out that, despite our advanced
scientific knowledge and technology, we failed at outfoxing evolution - when we
attack Malaria germs with drugs, the germs fight back. Scientists have discovered that the Plasmodium parasites
have repeatedly evolved to resist the front-line treatments. The mosquitoes that carry the parasites have rapidly
evolved to resist the insecticides we poison them with. And now, scientist has found that some
malaria parasite can cause disease severe enough to cause evolutionary
selection pressures in human populations!
Dr. Anna Rosana-Urgell and her collegues from PNG Institute
In Medical Research found that Plasmodium
vivax malaria is the reason behind the abnormally high rates of Southeast
Asian Ovalovytosis (SAO), a hereditary erythrocytes (red blood cell) disorder,
in the Asian and Oceanic region.
In SAO, the red blood
cells are a different shape (elliptical) from the usual biconcave disc shape. This genetic defect is carried by up to 35%
of people living on the coasts of Papua New Guinea, an area happened to have
high malaria endemic. The researchers
performed genetic tests in 1,975 children and found that nearly 50% of children
in Papua New Guinea aged 0-14 years are SAO-positive and immune to P. vivax. This means that SAO genetic defect may have
protective effect against malaria caused by P.vivax
by altering the ability of the parasite to develop within the red blood cell. These findings indicated that P.vivax have caused enough evolutionary pressure that it has influence genetic adaption of
the human population.
As Professor
Andrew Read, a biologies and entomologist from Penn State University, presented
at TEDMED: disease superbugs have the ability to mutate faster than treatments
are developed, and understanding natural selection can help scientists fight
back and control antibiotic resistance.
Word count: 444
Phyo, A.P. et al. Emergence of artemisinin-resistant malaria on the western border of Thailand: a longitudinal study, The Lancet, Volume 379, Issue 9830, 26 May–1 June 2012, Pages 1960-1966,(http://www.sciencedirect.com/science/article/pii/S014067361260484X)
Rosanas-Urgell A, Lin
E, Manning L, Rarau P, Laman M, et al. (2012) Reduced Risk of Plasmodium
vivax Malaria in Papua New Guinean Children with Southeast Asian
Ovalocytosis in Two Cohorts and a Case-Control Study. PLoS Med 9(9): e1001305.
doi:10.1371/journal.pmed.1001305
How similar is SAO to sickle cell disease? They sound remarkably similar, both causing a change in erythrocyte shape and conferring resistance to malaria.
ReplyDeleteSAO is similar to sickle cell disease in the way they manipulate human population through evolution. SAO causes the red blood cells to diform to a different shape (elliptical).
DeleteHave you looked into artemisinin-combination therapy? While it's not exactly a vaccine, it is very useful in treating malaria today. It uses two different antimalarials and combines them to deliver treatment. The assumption is that even if the parasite develops resistance to one drug, it is unlikely for it to evolve resistance to the other. Pretty cool.
ReplyDelete-Tom Xia
Awesome! I will look into that.
DeleteHow possible would it be then for humans to evolve resistant to other pathogens such as HIV by developing different cells that can perform the same function (and self-propagate)? I suppose that would be a little far-fetched though considering we would be attempting to CREATE life, although we could simply modify already-existing cells?
ReplyDeleteIt is definitely possible, at least theoretically. However HIV is fundamentally different from SAO and Malaria so I will need more research to answer that question.
DeleteMosquitoes are carriers for malaria, not the agents. I am not sure the beginning description of mosquitoes is accurate. But it is interesting how other genetic diseases causing irregular RBC shape (like sickle cells) enhances the survival change against malaria.
ReplyDeleteDoes SAO have a similar impact on human health as sickle-cell? I am curious as to whether an elliptical shape would cause as many issues as a sickle shape. Very interesting how malaria has caused so much evolutionary pressure to cause such similar mutations in different parts of the world.
ReplyDelete-Jesse Passman
Yes, definitely, at least on the mechanism ground.
DeleteThis is my first time to hear about SAO. It interesting because I feel like SAO has similar effect with sickle cell trait especially on Malaria immunity .
ReplyDeleteAlso the idea behind artemisinin-combination therapy mentioned by Tom sounds very similar to that of Antiviral therapy against HIV. I found it intriguing!
Yup! They are both fascinating topics
DeleteI think it is very interesting that malaria has precipitated the spread of both sickle cell anemia and South Asian Ovalovytosis in the African and Asian populations, respectively. It’s fascinating how the human body can provide a defense against a disease which modern medicine is not yet able to. You mentioned that malaria evolves rapidly – Are there any similarities between the mechanisms malaria and HIV use to do this? And do you think modern medicine is selecting for diseases which evolve rapidly, or does it just seem this way due to their prevalence in mass media?
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