Multiple, Independent T Cell Lymphomas Arising in an Experimentally FIV-Infected Cat during the Terminal Stage of Infection

被引:11
作者
Murphy, Brian G. [1 ]
Eckstrand, Christina [2 ]
Castillo, Diego [1 ]
Poon, Andre [1 ]
Liepnieks, Molly [1 ]
Harmon, Kristy [1 ]
Moore, Peter [1 ]
机构
[1] Univ Calif Davis, Sch Vet Med, Dept Pathol Microbiol & Immunol, Davis, CA 95616 USA
[2] Washington State Univ, Coll Vet Med, Dept Vet Microbiol & Pathol, Pullman, WA 99163 USA
来源
VIRUSES-BASEL | 2018年 / 10卷 / 06期
关键词
FIV (feline immunodeficiency virus); lymphoma; FAIDS (feline AIDS); cat; immunopathology; FELINE IMMUNODEFICIENCY VIRUS; (FIV)-ASSOCIATED LYMPHOMA; CLINICAL-ASPECTS; GENE-EXPRESSION; ACTIVATION; REPEAT; AP-1; IMMUNOPHENOTYPE; MACROPHAGES; PROMOTER;
D O I
10.3390/v10060280
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Our laboratory has serially reported on the virologic and immunopathologic features of a cohort of experimental feline immunodeficiency virus (FIV)-infected cats for more than eight years. At 8.09 years post infection (PI), one of these animals entered the terminal stage of infection, characterized by undulating hyperthermia, progressive anorexia, weight loss, and pancytopenia; the animal was not responsive to therapeutic interventions, necessitating euthanasia six weeks later (8.20 years PI). Subsequent analyses indicated that neoplastic lymphocytes infiltrated multiple cervical lymph nodes and a band-like region of the mucosal lamina propria within a segment of the intestine. Immunohistochemistry and T cell clonality testing determined that the nodal and intestinal lesions were independently arising from CD3 T cell lymphomas. In-situ RNA hybridization studies indicated that diffuse neoplastic lymphocytes from the cervical lymph node contained abundant viral nucleic acid, while viral nucleic acid was not detectable in lymphocytes from the intestinal lymphoma lesion. The proviral long terminal repeat (LTR) was amplified and sequenced from multiple anatomic sites, and a common clone containing a single nucleotide polymorphism was determined to be defective in response to phorbol myristate acetate (PMA)-mediated promoter activation in a reporter gene assay. This assay revealed a previously unidentified PMA response element within the FIV U3 region 3' to the TATA box. The possible implications of these results on FIV-lymphoma pathogenesis are discussed.
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页数:16
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