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  • How is poliovirus transmitted?
  • Compare the pros and cons of each of the two polio vaccines.

Transmissible spongiform encephalopathies

Acellular infectious agents called prions are responsible for a group of related diseases known as transmissible spongiform encephalopathies (TSEs) that occurs in humans and other animals (see Viroids, Virusoids, and Prions ). All TSEs are degenerative, fatal neurological diseases that occur when brain tissue becomes infected by prions. These diseases have a slow onset; symptoms may not become apparent until after an incubation period of years and perhaps decades, but death usually occurs within months to a few years after the first symptoms appear.

TSEs in animals include scrapie , a disease in sheep that has been known since the 1700s, and chronic wasting disease , a disease of deer and elk in the United States and Canada. Mad cow disease is seen in cattle and can be transmitted to humans through the consumption of infected nerve tissues. Human prion diseases include Creutzfeldt-Jakob disease and kuru , a rare disease endemic to Papua New Guinea.

Prions are infectious proteinaceous particles that are not viruses and do not contain nucleic acid. They are typically transmitted by exposure to and ingestion of infected nervous system tissues, tissue transplants, blood transfusions, or contaminated fomites. Prion proteins are normally found in a healthy brain tissue in a form called PrP C . However, if this protein is misfolded into a denatured form (PrP Sc ), it can cause disease. Although the exact function of PrP C is not currently understood, the protein folds into mostly alpha helices and binds copper. The rogue protein, on the other hand, folds predominantly into beta-pleated sheets and is resistant to proteolysis. In addition, PrP Sc can induce PrP C to become misfolded and produce more rogue protein ( [link] ).

As PrP Sc accumulates, it aggregates and forms fibrils within nerve cells. These protein complexes ultimately cause the cells to die. As a consequence, brain tissues of infected individuals form masses of neurofibrillary tangles and amyloid plaques that give the brain a spongy appearance, which is why these diseases are called spongiform encephalopathy ( [link] ). Damage to brain tissue results in a variety of neurological symptoms. Most commonly, affected individuals suffer from memory loss, personality changes, blurred vision, uncoordinated movements, and insomnia. These symptoms gradually worsen over time and culminate in coma and death.

The gold standard for diagnosing TSE is the histological examination of brain biopsies for the presence of characteristic amyloid plaques, vacuoles, and prion proteins. Great care must be taken by clinicians when handling suspected prion-infected materials to avoid becoming infected themselves. Other tissue assays search for the presence of the 14-3-3 protein, a marker for prion diseases like Creutzfeldt-Jakob disease. New assays, like RT-QuIC (real-time quaking-induced conversion), offer new hope to effectively detect the abnormal prion proteins in tissues earlier in the course of infection. Prion diseases cannot be cured. However, some medications may help slow their progress. Medical support is focused on keeping patients as comfortable as possible despite progressive and debilitating symptoms.

Endogenous PrPC interacts with mutant version PrPSC. This converts PrPC inot PrPSC. This leads to an accumulation of PRPSC. Each PRPSC can convert more PRPC. The options are: spontaneous generation of PRPSC, conversation of mutant PRP into PRPSC, and inoculation of PRPSC.
The replicative cycle of misfolded prion proteins.
  • Do prions reproduce in the conventional sense?
  • What is the connection between prions and the removal of animal byproducts from the food of farm animals?

Acellular infections of the nervous system

Serious consequences are the common thread among these neurological diseases. Several cause debilitating paralysis, and some, such as Creutzfeldt-Jakob disease and rabies, are always or nearly always fatal. Since few drugs are available to combat these infections, vector control and vaccination are critical for prevention and containment. [link] summarizes some important viral and prion infections of the nervous system.

Table titled: Acellular Infections of the Nervous System. Columns: Disease; Pathogen; Signs and Symptoms; Transmission; Diagnostic Tests; Antimicrobial Drugs; Vaccine. Disease: Arboviral encephalitis (eastern equine, western equine, St. Louis, West Nile, Japanese); EEEV, WEEV, SLEV, WNV, JEV; In mild cases, fever, chills, headaches, and restlessness; in serious cases, encephalitis leading to convulsions, coma, and death; From bird reservoirs to humans (and horses) by mosquito vectors of various species; Serologic testing of serum or CSF; None; Human vaccine available for JEV only; no vaccines available for other arboviruses. Disease: Creutzfeldt-Jacob Disease and other TSEs; Prions; Memory loss, confusion, blurred vision, uncoordinated movement, insomnia, coma, death; Exposure to infected nerve tissue via consumption or transplant, inherited; Tissue biopsy; no drug or vaccine. Disease: Poliomyelitis; Poliovirus; Asymptomatic or mild nausea, fever, headache in most cases; in neurological infections, flaccid paralysis and potentially fatal respiratory paralysis; Fecal-oral route or contact with droplets or aerosols ; Culture of poliovirus, PCR; None; Attenuated vaccine (Sabin), killed vaccine (Salk). Disease: Rabies; Rabies virus (RV); Fever, headaches, hyperactivity, hydrophobia, excessive salivation, terrors, confusion, spreading paralysis, coma, always fatal if not promptly treated; From bite of infected mammal; Viral antigen in tissue, antibodies to virus; Attenuated vaccine, rabies immunoglobulin; Attenuated vaccine. Disease: Viral meningitis; HSV-1, HSV-2, varicella zoster virus, mumps virus, influenza virus, measles virus; Nausea, vomiting, photophobia, stiff neck, confusion, symptoms generally resolve within 7–10 days; Sequela of primary viral infection; Testing of oral, fecal, blood, or CSF samples; Varies depending on cause; Varies depending on cause. Disease: Zika virus infection; Zika virus Fever, rash, conjunctivitis; in pregnant women, can cause fetal brain damage and microcephaly; Between humans by Aedes spp. mosquito vectors, also may be transmitted sexually or via blood transfusion; Zika virus RNA assay, Trioplex RT-PCR, Zika MAC-ELISA test; No drug or vaccine.

Key concepts and summary

  • Viral meningitis is more common and generally less severe than bacterial menigitis. It can result from secondary sequelae of many viruses or be caused by infections of arboviruses.
  • Various types of arboviral encephalitis are concentrated in particular geographic locations throughout the world. These mosquito-borne viral infections of the nervous system are typically mild, but they can be life-threatening in some cases.
  • Zika virus is an emerging arboviral infection with generally mild symptoms in most individuals, but infections of pregnant women can cause the birth defect microcephaly.
  • Polio is typically a mild intestinal infection but can be damaging or fatal if it progresses to a neurological disease.
  • Rabies is nearly always fatal when untreated and remains a significant problem worldwide.
  • Transmissible spongiform encephalopathies such as Creutzfeldt-Jakob disease and kuru are caused by prions. These diseases are untreatable and ultimately fatal. Similar prion diseases are found in animals.

Fill in the blank

The rogue form of the prion protein is called ________.

PrP Sc

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________ are the most common reservoir for the rabies virus worldwide.

Dogs

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________ was the scientist who developed the inactivated polio vaccine.

Jonas Salk

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________ is a prion disease of deer and elk.

Chronic wasting disease

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The rogue form of prion protein exists primarily in the ________ conformation.

beta sheet

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Short answer

Explain how a person could contract variant Creutzfeldt-Jakob disease by consuming products from a cow with bovine spongiform encephalopathy (mad cow disease).

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Source:  OpenStax, Microbiology. OpenStax CNX. Nov 01, 2016 Download for free at http://cnx.org/content/col12087/1.4
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