Prions: The Protein That Acts Like a Virus

 

Prions:Protein That Acts a Virus

Prion diseases, also known as transmissible spongiform encephalopathies (TSEs), represent a rare and devastating group of brain disorders that can affect both humans and animals. What makes these diseases particularly unique in the medical world is their cause: they are triggered by prions, which are normal proteins found in the brain that, for reasons not fully understood, suddenly twist and fold into an abnormal shape. This misfolded prion then acts as a template, prompting other healthy proteins to misfold in the same way, leading to a self-propagating and destructive cascade throughout the brain.

 As these abnormal prions accumulate, they cause progressive damage by creating tiny holes in the brain tissue. When examined under a microscope, the brain tissue resembles a sponge full of small holes, which is where the term “spongiform” comes from. The onset of these diseases is typically rapid and, tragically, mostly seen in older adults—the median age at diagnosis is around 67 years. Once symptoms appear, the progression is merciless: affected individuals often deteriorate quickly, with the time from the first signs of illness to death usually measured in a few months, sometimes extending up to a year at most. The decline is not gradual; instead, it is a steep and unrelenting descent.

                                                      A : Normal brain              B: Prions affected Brain

Prions themselves are extraordinarily resilient. Ordinary methods of sterilization—such as boiling, exposure to radiation, or even most commonly used disinfectants—are ineffective at destroying them. This remarkable resistance makes prions a significant concern in hospital and laboratory settings, where contamination can be extremely difficult to control and poses a risk for accidental transmission.

 

Types of prion diseases with its own characteristics and modes of transmission:

 

1. Creutzfeldt-Jakob Disease (CJD) is the most common form seen in humans. In the majority of cases, it arises sporadically, with no identifiable cause or risk factor; the prion misfolding seems to occur spontaneously.

2.Variant Creutzfeldt-Jakob Disease (vCJD) is different in origin. It has been linked to the consumption of beef products contaminated with prions from cattle suffering from bovine spongiform encephalopathy, more widely known as “Mad Cow Disease.”

3.Fatal Familial Insomnia is an inherited prion disease. It specifically targets the thalamus, a deep brain structure crucial for regulating sleep, leading to intractable insomnia and eventually widespread neurological deterioration.

4.Kuru is a historically significant prion disease that was identified among the Fore people of Papua New Guinea. It was transmitted through the practice of ritual cannibalism, particularly the consumption of brain tissue from deceased relatives.

5.Chronic Wasting Disease affects wildlife, primarily deer, elk, and moose. While it has caused significant concern among hunters and wildlife officials, to date there have been no confirmed cases of transmission to humans.

 Symptoms

 The early symptoms of prion diseases are often subtle and easily mistaken for other neurological or psychiatric conditions. These may include rapidly progressing dementia, dramatic changes in personality, and memory impairment. As the disease advances, more pronounced neurological symptoms emerge, such as sudden and involuntary muscle jerks known as myoclonus, problems with balance and coordination (ataxia), visual disturbances, and in some cases, hallucinations.

                                                          Fig:Symptoms of Prions Disease

 Diagnosis

Diagnosing prion diseases is complex and relies on assembling multiple pieces of evidence. Physicians may use MRI scans to detect characteristic patterns such as “cortical ribboning,” while EEGs can reveal abnormal electrical activity. A specialized laboratory test called RT-QuIC, performed on spinal fluid, can provide strong supportive evidence. However, the only definitive way to confirm a diagnosis is by examining brain tissue after death, which reveals the hallmark spongiform changes.

 Prevention and Cure

Currently, there is no cure for prion diseases, nor are there any treatments that can slow or halt their progression. Medical care is focused on providing comfort, managing symptoms, and supporting patients and their families through the course of the illness.