Literature DB >> 18612634

MAIDS resistance-associated gene expression patterns in secondary lymphoid organs.

Suprawee Tepsuporn1, Jedediah N Horwitt, George W Cobb, Sharon A Stranford.   

Abstract

Murine acquired immunodeficiency syndrome (MAIDS) is caused by exposure to murine leukemia virus and serves as a model to study human AIDS. In MAIDS-susceptible C57BL/6 mice, virus exposure leads to progressive immune deficiency, while resistant strains such as BALB/c recover from infection and develop protective immunity. The goal of this study was to identify early gene expression patterns that may be important in establishing this strain-specific differential response. Total RNA was isolated from spleens and pooled lymph nodes of both mouse strains at 3 and 7 days post virus infection. The complementary DNA generated from this RNA was hybridized to mouse oligonucleotide DNA microarrays using a strategy that controlled for inherent variability and highlighted only virus-induced changes. Fluorescent intensities were normalized and analyzed for statistically significant differential expression between strains across both time points and lymphoid organs. The majority of the resistance-associated genes was identified at day 3 post-infection and demonstrated the highest fold differences between strains, while more susceptibility-associated sequences were seen at 7 days post-infection. Among the most highly differentially expressed sequences seen at the earlier time point were genes related to protein metabolism, especially serine proteases. Differential patterns of chemokine-related genes were observed at the later time point. The overall pattern of expression suggests strain-specific differences in proteases and chemokines within secondary lymphoid organs shortly after infection influence the likelihood of disease progression.

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Year:  2008        PMID: 18612634     DOI: 10.1007/s00251-008-0312-4

Source DB:  PubMed          Journal:  Immunogenetics        ISSN: 0093-7711            Impact factor:   2.846


  43 in total

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Review 2.  Neutrophil serine proteases: specific regulators of inflammation.

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Review 3.  Natural post-translational modifications of chemokines.

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4.  The CD154/CD40 interaction required for retrovirus-induced murine immunodeficiency syndrome is not mediated by upregulation of the CD80/CD86 costimulatory molecules.

Authors:  Kathy A Green; W James Cook; Arlene H Sharpe; William R Green
Journal:  J Virol       Date:  2002-12       Impact factor: 5.103

5.  Retrovirus-induced murine acquired immunodeficiency syndrome: natural history of infection and differing susceptibility of inbred mouse strains.

Authors:  J W Hartley; T N Fredrickson; R A Yetter; M Makino; H C Morse
Journal:  J Virol       Date:  1989-03       Impact factor: 5.103

Review 6.  The spreading of HIV-1 infection in the human organism is caused by fractalkine trafficking of the infected lymphocytes--a review, hypothesis and implications for treatment.

Authors:  Yechiel Becker
Journal:  Virus Genes       Date:  2007-04       Impact factor: 2.332

7.  Resistance to murine AIDS in offspring of mice infected with LP-BM5. Role of CD8 T cells.

Authors:  J H Pavlovitch; E Hulier; M Rizk-Rabin; M Marussig; D Mazier; M L Joffret; S Hoos; M Papiernik
Journal:  J Immunol       Date:  1996-06-15       Impact factor: 5.422

8.  Opportunistic infections and retrovirus-induced immunodeficiency: studies of acute and chronic infections with Toxoplasma gondii in mice infected with LP-BM5 murine leukemia viruses.

Authors:  R T Gazzinelli; J W Hartley; T N Fredrickson; S K Chattopadhyay; A Sher; H C Morse
Journal:  Infect Immun       Date:  1992-10       Impact factor: 3.441

9.  Impact of MHC class I gene on resistance to murine AIDS.

Authors:  M Makino; D B Murphy; R W Melvold; J W Hartley; H C Morse
Journal:  Scand J Immunol       Date:  1995-09       Impact factor: 3.487

10.  Quantitative analysis of LP-BM5 murine leukemia retrovirus RNA using real-time RT-PCR.

Authors:  W James Cook; Kathy A Green; Joshua J Obar; William R Green
Journal:  J Virol Methods       Date:  2003-03       Impact factor: 2.014

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