Full-length DNAs of the Coleman and S7801 strains (pSKY3.0, pSKY5.0) of infectious feline foamy viruses (FFVs) were cloned and sequenced. Parental viruses, designated SKY3.0 and SKY5.0, were secreted following transfection of Crandell feline kidney (CRFK) cells. Production of the rescued parental viruses was enhanced in the presence of trichostatin A. Amino acid sequence similarities between FFV and human foamy virus (HFV) are extremely low for the envelope protein and capsid antigen, as predicted from the two clones. However, a chimeric FFV clone was constructed with the HFV Env substituted for the FFV Env. The chimeric virus (HFFV, SKY4.0) was able to infect and replicate in CRFK cells as well as in peripheral blood mononuclear cells of cats in vivo. Consequently, the chimeric HFFV may be useful for the creation of FV vectors for gene transfer strategies.

Download full-text PDF

Source
http://dx.doi.org/10.1099/0022-1317-82-12-2999DOI Listing

Publication Analysis

Top Keywords

foamy virus
12
feline foamy
8
parental viruses
8
crfk cells
8
isolation sequencing
4
sequencing infectious
4
infectious clones
4
clones feline
4
foamy
4
virus
4

Similar Publications

We obtained the near-complete simian foamy virus (SFV) genome from an infected human bitten by an African green monkey ( SFVcae_hu501). The genome is 13,062 nucleotides long with the classical SFV genome structure. Phylogenetically, SFVcae_hu501 clustered closely with SFV from (SFVagm_LK3).

View Article and Find Full Text PDF

Discovery of two novel foamy viruses in sea lions and dolphins provides insight into their evolutionary history.

Infect Genet Evol

December 2024

Hainan Medical University-The University of Hong Kong Joint Laboratory of Tropical Infectious Diseases, Key Laboratory of Tropical Translational Medicine of Ministry of Education, School of Basic Medicine and Life Sciences, NHC Key Laboratory of Tropical Disease Control, Hainan Medical University, Haikou 571199, China. Electronic address:

The prevalence and evolution of foamy viruses (FVs) have become the focus of research because of the risk of new zoonotic diseases. FVs have been isolated from various mammals and exhibit long-term co-speciation with their hosts. They also appear to be mild and nonpathogenic to their hosts.

View Article and Find Full Text PDF

Advances in foamy virus vector systems: Development and applications.

Virology

January 2025

Department of Systems Biotechnology, Chung-Ang University, Anseong, 17456, Republic of Korea. Electronic address:

Foamy virus (FV) is a retrovirus with a safer integration profile than other retroviruses, rendering it appealing for gene therapy. Prototype FV (PFV) vector systems have been devised to yield high-titer vectors carrying large transgenes. Subsequent iterations of PFV vectors have been engineered to be replication-incompetent, enhancing their safety.

View Article and Find Full Text PDF

Hepatitis C-Induced Immunoglobulin A (IgA) Nephropathy: An Uncommon Cause of Hematuria.

Cureus

September 2024

General Medicine, Saveetha Medical College and Hospital, Saveetha Institute of Medical and Technical Sciences, Saveetha University, Chennai, IND.

Article Synopsis
  • IgA nephropathy, or Berger's disease, is marked by IgA deposits in the kidney and can lead to serious conditions like rapidly progressive glomerulonephritis.
  • Hepatitis C virus (HCV) is mainly known for liver issues but can also cause renal problems; however, IgA nephropathy linked to HCV is rare.
  • A case study of a 24-year-old man with untreated HCV showed serious kidney issues leading to a diagnosis of IgA nephropathy, but treatment improved his condition, highlighting the need for awareness and early intervention in HCV-related kidney complications.
View Article and Find Full Text PDF

Background: Cytokine storm syndromes (CSSs), including hemophagocytic lymphohistiocytosis (HLH), are increasingly recognized as hyperinflammatory states leading to multiorgan failure and death. Familial HLH in infancy results from homozygous genetic defects in perforin-mediated cytolysis by CD8 T lymphocytes and natural killer (NK) cells. Later-onset CSSs are often associated with heterozygous defects in familial HLH genes, but genetic etiologies for most are unknown.

View Article and Find Full Text PDF

Want AI Summaries of new PubMed Abstracts delivered to your In-box?

Enter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!