The novel human polyomaviruses HPyV6, 7, 9 and beyond

Bernhard Ehlers1, Ulrike Wieland

  • 1Division 12 Measles, Mumps, Rubella, and Viruses Affecting Immunocompromised Patients, Robert Koch-Institute, Berlin, Germany. ehlersb@rki.de

Insights

Six new human polyomaviruses (HPyVs) lack disease associations, though they are shed by healthy individuals and patients. Further research is needed to understand their reservoirs and potential links to cancer.

Area of Science:

  • Virology
  • Oncology
  • Epidemiology

Background:

  • Merkel cell polyomavirus (MCC) is linked to Merkel cell carcinoma (MCC).
  • Six novel human polyomaviruses (HPyVs) have been identified: HPyV6, HPyV7, HPyV9, HPyV10, HPyV12, and Saint Louis polyomavirus (STLPyV).
  • These HPyVs are not yet associated with any specific diseases.

Purpose of the Study:

  • To investigate the shedding and detection of novel HPyVs in various human populations.
  • To explore potential associations between these HPyVs and human cancers or other diseases.
  • To understand the prevalence and circulation of HPyVs in the human population.

Main Methods:

  • Polymerase chain reaction (PCR) was used to detect HPyV shedding in skin, body fluids, and excretions.
  • HPyV presence was analyzed in stool samples from children and in organs from patients with malignant diseases.
  • Serological studies using enzyme-linked immunosorbent assays (ELISA) with capsomer-based or virus-like particles (VLPs) were performed to assess HPyV circulation.

Main Results:

  • HPyV6 and HPyV7 are shed from the skin of healthy individuals and patients with skin tumors.
  • HPyV6, HPyV7, and HPyV9 were sporadically detected in body fluids of immunocompromised and healthy individuals.
  • HPyV10 variants and STLPyV were found in stool samples, while HPyV12 was detected in digestive tract organs. Serological data indicate HPyV6, HPyV7, HPyV9, and HPyV12 circulate in the human population.

Conclusions:

  • Novel HPyVs are widespread in the human population, with HPyV6 and HPyV7 commonly shed from the skin.
  • Despite encoding potentially oncogenic T antigens, current evidence does not strongly associate HPyV6, HPyV7, and HPyV9 with human tumors.
  • Future research should focus on identifying the reservoirs of these novel HPyVs and investigating their roles in both malignant and non-malignant diseases.

Related Concept Videos

Human Virome01:26

Human Virome

The human body harbors a vast and diverse viral community known as the human virome. The virome includes bacteriophages that infect bacteria, and eukaryotic viruses that infect human cells. Transient dietary and environmental viruses also contribute to this dynamic ecosystem. Estimates suggest the human body may contain on the order of 10¹³ viral particles, though abundance varies widely by body site and detection method.Comprehensive characterization of the virome has become possible only with...
Retroviruses02:33

Retroviruses

Retroviruses and retrotransposons both insert copies of their genetic elements into the genome of the host cell. Thus, the viral genes are passed on when the host genome is replicated or translated. A typical retroviral DNA sequence contains 3-4 genes that encode the different proteins required for its structural assembly and function as a molecular parasite. This DNA is transcribed into a single mRNA, which is very similar in structure to conventional mRNAs, i.e., it is capped at the 5’...
Subviral Agents01:29

Subviral Agents

Subviral agents are infectious entities that resemble viruses but lack one or more viral components, such as a capsid or essential replication machinery. These agents include viroids, prions, and satellites, each possessing distinct structural and functional characteristics that influence their mode of infection and replication.Viroids are the simplest subviral agents, consisting of circular, single-stranded RNA molecules without a protein coat. They exclusively infect plants, relying entirely...
Viruses with RNA Genomes01:29

Viruses with RNA Genomes

RNA viruses are categorized into positive-strand, negative-strand, or double-stranded groups based on their genomic structure and replication mechanisms. This classification dictates how they exploit host cellular machinery for protein synthesis and replication. Some RNA viruses also utilize reverse transcription as part of their life cycle, further diversifying their replication strategies.Positive-Strand RNA VirusesPositive-strand RNA viruses have genomes that function directly as messenger...
Retrovirus Life Cycles01:10

Retrovirus Life Cycles

Retroviruses have a single-stranded RNA genome that undergoes a special form of replication. Once the retrovirus has entered the host cell, an enzyme called reverse transcriptase synthesizes double-stranded DNA from the retroviral RNA genome. This DNA copy of the genome is then integrated into the host’s genome inside the nucleus via an enzyme called integrase. Consequently, the retroviral genome is transcribed into RNA whenever the host’s genome is transcribed, allowing the retrovirus to...
Viral Hepatitis I: Introduction01:28

Viral Hepatitis I: Introduction

Viral hepatitis is an inflammatory condition of the liver caused by infection with hepatotropic viruses, most commonly hepatitis A, B, C, D, and E. Despite variations in structure and transmission, all viruses mentioned infect hepatocytes and provoke immune responses that can hinder liver function. Additionally, some non-hepatotropic viruses can also lead to hepatic inflammation.Hepatitis A VirusHepatitis A virus (HAV) is transmitted through the fecal–oral route, typically by ingestion of food...