Kuhl: Genetic Mutations Could Provide Protection Against Brain Diseases Linked to Cannibalism

Genetic research in a very remote community in Papua New Guinea has revealed new insights into a brain disease that is spread when people eat dead relatives and has killed thousands of people over two decades.

Dotted with mountains, gorges, and fast-flowing rivers, Papua New Guinea’s Eastern Highlands province is extremely isolated from the rest of the world, and it wasn’t until the beginning of the 20th century that outsiders realized that about 1 million people lived there.

Some tribes known as the Fore practiced a form of cannibalism called “funeral feasts,” in which they consumed the bodies of their deceased relatives as part of their funeral rites. This could mean they ingested an abnormally folded protein called a prion, which can cause a fatal neurodegenerative condition called kuru associated with Creutzfeldt-Jakob disease (CJD). However, the local people believed that the Kuru phenomenon was caused by witchcraft. At least 2,700 Kuru deaths have been recorded in the eastern highlands.

Simon Mead Researchers at University College London examined the genomes of 943 people representing 68 villages and 21 language groups in the region. Although this region of Papua New Guinea covers just over 11,000 square kilometers, smaller than Jamaica, researchers say the different groups are as genetically different as the peoples of Finland and Spain, some 3,000 kilometers apart.

The study found that not everyone who attended the funeral died from the disease. Mead and his colleagues say it appears communities were beginning to develop a resistance to kuru, which led to tremors, loss of coordination, and, ultimately, death.

The study found that some of the elderly women who survived the feast had mutations in the gene encoding the prion protein, which likely conferred resistance to kuru disease.

By the 1950s, funeral feasts had become illegal, and the kuru epidemic began to subside, but visitors say that the number of women in some villages had dwindled because so many women had died from kuru. It pointed out. Mead said women and children are most susceptible to the disease, likely because they ate the brains of deceased relatives.

However, genetic evidence shows that despite fears of the disease, there was a large influx of women into Fora tribal areas, particularly in areas where the highest levels of kuru were present.

“We believe it is likely that the sexual prejudice caused by Kuru caused single men in Kuru-affected communities to look further afield for wives than usual because they were unable to find potential wives locally. “We will,” Meade said.

He said the team wants to understand what factors confer resistance to prion diseases such as CJD, which caused a severe epidemic in the UK in the 1990s.

“[Our work sets] “This is a site to detect genetic factors that may have helped the Fore people resist kuru,” Mead said. “Such resistance genes may suggest therapeutic targets.”

Ira Debson Researchers from the Garvan Institute of Medical Research in Sydney, Australia, say the study provides new insight into the “rich and unique cultural, linguistic and genomic diversity” of the Eastern Highlands region.

“This is a demonstration of how genomics can be used to look almost back in time, reading the genetic signature of past epidemics and understanding how they have shaped today’s populations. It helps.”