Malaria caused by Plasmodium parasites is a life- threatening infectious disease that kills at least half a million people annually while causing over 200 million new infections.
In some cases, complications can quickly develop such as cerebral malaria, respiratory distress and severe anaemia, often leading to death.
The majority of patients recover from disease, however, there is increasing evidence to suggest that survivors experience long-term 'hidden' pathologies due to infection that are as yet poorly defined.
Now, researchers at the Osaka University in Japan have used mouse malaria models to show that robust immune activation and invasion of parasite by-products into the bone marrow during and after infection leads to an adverse balance in bone homeostasis by bone forming osteoblasts and bone resorbing osteoclasts.
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"We found that Plasmodium products continuously accumulate in the bone marrow niche which turns the bone noticeably black in colour, and results in it being "eaten-up" by bone resorbing cells known as osteoclasts, eventually disrupting bone homeostasis," said Michelle Lee, the first author of the study.
These products induce MyD88-dependent inflammatory responses in osteoclast and osteoblast precursors, leading to increased RANKL expression - a key molecule inducing osteoclast differentiation - and over-stimulation of osteoclastogenesis favouring bone resorption.
"Although chronic inflammatory conditions are known to facilitate bone disorders, our study - for the first time - shows that malaria can do the same thing, with hallmark 'signatures' left in the bone tissue, a very unique feature of malaria infection," said Coban.
"One may think that the infection has been completely cured by anti-malarial treatment, and be feeling fully recovered, however, sustained long-term accumulation of parasite by-products leave the bone in a state of chronic inflammation, leading to long term bone loss," Coban said.
The study shows that there is a simple way to reverse the side effects of malaria infection on bone.
Oral supplementation with alfacalcidol, a vitamin D3 analogue, could completely prevent bone loss.
Anti-malarials coupled with bone therapy may be beneficial in improving bone health in malaria-infected individuals.