Molecular Mechanisms and Clinical Manifestations of Persistent Viral Infections (2nd Edition)
A special issue of Viruses (ISSN 1999-4915). This special issue belongs to the section "Human Virology and Viral Diseases".
Deadline for manuscript submissions: 1 February 2027 | Viewed by 25
Special Issue Editors
Interests: HPV; HIV; viral hepatitis; virus molecular evolution; host–pathogen interaction; zoonoses
Special Issues, Collections and Topics in MDPI journals
Interests: antiviral drugs; respiratory viruses; virus morphogenesis; viral glycoproteins
Special Issues, Collections and Topics in MDPI journals
Special Issue Information
Dear Colleagues,
Persistent viral infections are recognized as an important cause of morbidity and mortality in humans and are also responsible for silent pandemics (e.g., HIV, HBV, and HCV) that cause several million deaths each year worldwide.
Many viruses can remain in the host for a long time, even a lifetime, after acute infection, by establishing persistence in different cell types, which represent an important reservoir for the dissemination of the virus in the environment, and spreading to other hosts in an asymptomatic manner, as well as symptomatic or paucisymptomatic clinical manifestations.
Several factors contribute to the establishment and maintained persistence of a virus in a host, such as the absence of cytopathic effects or the restriction of viral replication; the maintenance of the viral genome in host cells in extrachromosomal form (episome) or integrated into the cellular genome; or, most importantly, the ability to escape the eradication of the virus by the immune system, whether or not this is associated with the activation of the inflammatory response, which may be a significant part of pathogenesis. There are three types of persistent virus–host infections: (1) chronic infection, characterized by the presence of the virus at a low viral load that can cause minimal continuous damage over time, leading to organ impairment and clinical manifestation of the disease (e.g., HBV, HCV); (2) latent infection in which the viral genome is maintained in the absence of the production of infectious viral particles and only after successive reactivations from the latent state (recurrent infections), which may occur later in the host’s life, can the function of the target organ be compromised (e.g., keratoconjunctivitis from HSV); and (3) slow infection, which is characterized by a more extended incubation period followed by ongoing disease. Some viruses use this strategy to persist in the central nervous system (CNS), an immune-privileged site, and, over time, virus reactivation causes degenerative CNS disease (e.g., SSPE, Subacute Sclerosing Panencephalitis, from measles). Other viruses show immune escape by infecting cells of the immune system, as in the case of HIV, in which the proviral DNA integrates into the cellular genome of lymphocytes and macrophages and the virus establishes a slow infection that leads to AIDS many years later. For many RNA viruses capable of establishing persistent infections, the molecular mechanism by which the genome remains within host cells is still being studied (e.g., long COVID-19 from SARS-CoV-2). In some cases of persistent infection, injury is not associated with the death of infected cells but rather with immune-mediated cellular damage (e.g., hepatitis from HBV, HCV). Oncogenic viruses establish persistent infections, most of which do not lead to direct carcinogenesis, and tumor-directed progression depends on other pro-cancerogenic factors (Burkitt lymphoma from EBV); in other cases, however, tumors are strictly dependent on the viral expression of oncoproteins (e.g., cervical cancer from HPV or Rous sarcoma from Rous sarcoma virus). The process of endogenization of the human genome consists of acquisition via the integration of viral sequences into the DNA of the germ line cells of our ancestors during the evolutionary process, resulting from persistent infections with ancestral retroviruses. More recently, this has also been observed for non-retroviral viruses, such as Bornavirus. Antiviral drugs are the most commonly used therapeutic modality to counteract persistent infections, although eradicating the virus is very challenging. Among examples of pharmacological success are current anti-HCV drugs, which allow for the elimination of the virus in about 95% of infected individuals (e.g., Sofosbuvir for HCV cure). This Special Issue will present the most recent research on understanding molecular mechanisms, clinical manifestations, and therapeutic strategies during persistent viral infections.
You can read more publications in this series of Special Issues:
https://www.mdpi.com/journal/viruses/special_issues/Persistent_Viral_Infections.
Dr. Anna Rosa Garbuglia
Dr. Simone La Frazia
Guest Editors
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Keywords
- mammalian viruses
- chronic infection
- latent infection
- HIV
- HPV
- HBV
- HCV
- HSV
- pathogenetic mechanisms
- molecular pathways
- oncogenic processes
- immunity
- antiviral drugs
- endogenous viral element
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