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At Eddy's suggestion, the virus was dubbed polyoma, which means many tumors. The virus was named the Stewart-Eddy or SE polyoma virus, after their respective surnames. [1] The results of their collaboration earned them recognition by Time magazine in 1959, featuring a cover story on newly discovered viral agents that cause cancer. [1]
The primary alphapolyomavirus that is of clinical significance to humans is Merkel cell polyomavirus (Human polyomavirus 5, MCV, or MCPyV). The apparent oncogenicity of MCPyV [6] similar to other cancer-causing viruses such as HPV, Epstein-Barr virus, and Hepatitis C virus [7] is a main area of research for the scientific community.
At Eddy's suggestion, the virus was dubbed "polyoma," meaning many tumors. The virus was named the Stewart-Eddy or SE polyoma virus, after their respective surnames. [13] The results of their collaboration earned them recognition by Time magazine in 1959, featuring a cover story on newly discovered viral agents that cause cancer.
Polyomaviridae is a family of viruses whose natural hosts are primarily mammals and birds. [1] [2] As of 2024, there are eight recognized genera. [3]Fourteen species are known to infect humans, while others, such as Simian Virus 40, have been identified in humans to a lesser extent.
The virus is very common in the general population, infecting 70% to 90% of humans; most people acquire Human polyomavirus 2 in childhood or adolescence. [ 22 ] [ 23 ] [ 24 ] It is found in high concentrations in urban sewage worldwide, leading some researchers to suspect contaminated water as a typical route of infection.
All known human polyomaviruses are fairly common in healthy adult populations and are usually asymptomatic. In studies that profile polyomavirus seroprevalence, or prevalence of detectable antibodies against viral proteins indicating either past or present exposure in immunocompetent adults, estimates of HPyV6 prevalence have ranged from approximately 60–85%, with evidence of low prevalence ...
Merkel cell polyomavirus (MCV or MCPyV) was first described in January 2008 in Pittsburgh, Pennsylvania. [1] It was the first example of a human viral pathogen discovered using unbiased metagenomic next-generation sequencing with a technique called digital transcriptome subtraction. [2]
All known human polyomaviruses are fairly common in healthy adult populations and are usually asymptomatic. In studies that profile polyomavirus seroprevalence, or prevalence of detectable antibodies against viral proteins indicating either past or present exposure in immunocompetent adults, HPyV9 tends to have a relatively lower prevalence compared to other human polyomaviruses.