Polymerase chain reaction and partial sequencing of a British isolate (T637) of feline immunodeficiency virus

We have used the polymerase chain reaction (PCR) and direct sequencing of the amplified products to obtain information of the molecular nature of an FIV isolate, T637. Cats experimentally infected with T637 have progressed to clinical immunodeficiency disease. The 5′ long terminal repeat (LTR), most...

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Published inVeterinary microbiology Vol. 36; no. 3; pp. 369 - 377
Main Authors Grail, A., Harbour, D.A., Stokes, C.R., Gruffydd-Jones, T.J.
Format Journal Article
LanguageEnglish
Published Amsterdam Elsevier B.V 01.09.1993
Elsevier Science
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Abstract We have used the polymerase chain reaction (PCR) and direct sequencing of the amplified products to obtain information of the molecular nature of an FIV isolate, T637. Cats experimentally infected with T637 have progressed to clinical immunodeficiency disease. The 5′ long terminal repeat (LTR), most of the genes coding for internal proteins (GAG) and surface proteins (ENV), and part of the polymerase (POL) gene have been sequenced. The LTR of T637 has 92% nucleic acid identity with the prototype strain, FIV-Petaluma and the Glasgow isolate, FIV-14, 89% with a Swiss isolate, FIVZ2, and 95% with the PPR isolate. Both GAG and POL genes of T637 share extensive homology with Petaluma and PPR. In the ENV gene, T637 has 91% nucleic acid homology with Petaluma and 86% with PPR, and an overall amino acid homology of between 81–87%. For the surface (SU) region of the ENV gene product, T637 has 89% amino acid homology with Petaluma and FIVZ2 and 86% with PPR.
AbstractList We have used the polymerase chain reaction (PCR) and direct sequencing of the amplified products to obtain information of the molecular nature of an FIV isolate, T637. Cats experimentally infected with T637 have progressed to clinical immunodeficiency disease. The 5′ long terminal repeat (LTR), most of the genes coding for internal proteins (GAG) and surface proteins (ENV), and part of the polymerase (POL) gene have been sequenced. The LTR of T637 has 92% nucleic acid identity with the prototype strain, FIV-Petaluma and the Glasgow isolate, FIV-14, 89% with a Swiss isolate, FIVZ2, and 95% with the PPR isolate. Both GAG and POL genes of T637 share extensive homology with Petaluma and PPR. In the ENV gene, T637 has 91% nucleic acid homology with Petaluma and 86% with PPR, and an overall amino acid homology of between 81–87%. For the surface (SU) region of the ENV gene product, T637 has 89% amino acid homology with Petaluma and FIVZ2 and 86% with PPR.
Author Stokes, C.R.
Gruffydd-Jones, T.J.
Grail, A.
Harbour, D.A.
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Issue 3
Keywords Fissipedia
Immunopathology
Carnivora
Molecular structure
Nucleotide sequence
Retroviridae
Feline immunodeficiency virus
Veterinary medicine
Immune deficiency
Infection
Virus
Proteins
Polymerase chain reaction
Vertebrata
Experimental disease
Mammalia
Viral disease
DNA
Cat
Lentivirinae
Clinical isolate
Aminoacid sequence
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Snippet We have used the polymerase chain reaction (PCR) and direct sequencing of the amplified products to obtain information of the molecular nature of an FIV...
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StartPage 369
SubjectTerms AIDS/HIV
Amino Acid Sequence
ANIMAL VIRUSES
Animals
Base Sequence
Biological and medical sciences
CATS
CHAT
Cloning, Molecular
DEFICIENCE IMMUNOLOGIQUE
DEFICIENCIA INMUNOLOGICA
DNA, Viral - chemistry
feline immunodeficiency virus
Fundamental and applied biological sciences. Psychology
GATO
Gene Products, env - chemistry
Gene Products, gag - chemistry
Gene Products, pol - chemistry
Genes, env
Genes, gag
Genes, pol
Genetics
Immunodeficiency Virus, Feline - chemistry
Immunodeficiency Virus, Feline - genetics
IMMUNOLOGICAL DEFICIENCY
Microbiology
Molecular Sequence Data
Polymerase Chain Reaction
Repetitive Sequences, Nucleic Acid
Sequence Alignment
Viral Proteins - chemistry
Viral Proteins - genetics
Virology
VIRUS DE LOS ANIMALES
VIRUS DES ANIMAUX
Title Polymerase chain reaction and partial sequencing of a British isolate (T637) of feline immunodeficiency virus
URI https://dx.doi.org/10.1016/0378-1135(93)90103-E
https://www.ncbi.nlm.nih.gov/pubmed/8273281
https://search.proquest.com/docview/16895550
https://search.proquest.com/docview/76137091
Volume 36
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