Literature DB >> 17303259

A flow cytometry-based method for detecting antibody responses to murine cytomegalovirus infection.

Alice A Bickerstaff1, Peter D Zimmerman, Bret A Wing, Frederick Taylor, Joanne Trgovcich, Charles H Cook.   

Abstract

An assay based on target cells infected with green fluorescent protein labeled murine cytomegalovirus (GFP-MCMV) and dual color flow cytometry for detecting antibody to MCMV is described. After optimizing conditions for this technique, kinetics of anti-MCMV IgG antibody response was tested in susceptible (BALB/c) and resistant (C57BL/6) mouse strains following primary MCMV infection. Previously published antibody kinssetics were confirmed in susceptible mice, with peak IgG response seen approximately 8 weeks after primary infection, decreasing by 20 weeks after infection. In contrast, MCMV resistant C57BL/6 mice showed significantly lower IgG antibody responses than susceptible mice. Although several techniques have been previously described to detect murine antibody responses to MCMV, including nuclear anti-complement immunofluorescence, viral immunoblotting, complement fixation, indirect immunofluorescence, indirect hemagglutination, and enzyme-liked immunosorbent assay techniques, these techniques are all time consuming and laborious. The technique presented is a simple time efficient alternative to detect previous MCMV antibody responses in experimentally infected mice.

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Year:  2007        PMID: 17303259      PMCID: PMC1899410          DOI: 10.1016/j.jviromet.2007.01.006

Source DB:  PubMed          Journal:  J Virol Methods        ISSN: 0166-0934            Impact factor:   2.014


  54 in total

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2.  Disseminated fatal human cytomegalovirus disease after severe trauma.

Authors:  A Heininger; U Vogel; C Aepinus; K Hamprecht
Journal:  Crit Care Med       Date:  2000-02       Impact factor: 7.598

3.  Patterns of allosensitization in allograft recipients: long-term cardiac allograft acceptance is associated with active alloantibody production in conjunction with active inhibition of alloreactive delayed-type hypersensitivity.

Authors:  A M VanBuskirk; M E Wakely; J H Sirak; C G Orosz
Journal:  Transplantation       Date:  1998-04-27       Impact factor: 4.939

4.  Enhanced green fluorescent protein as a marker for localizing murine cytomegalovirus in acute and latent infection.

Authors:  S C Henry; K Schmader; T T Brown; S E Miller; D N Howell; G G Daley; J D Hamilton
Journal:  J Virol Methods       Date:  2000-09       Impact factor: 2.014

5.  Focal transcriptional activity of murine cytomegalovirus during latency in the lungs.

Authors:  S K Kurz; M Rapp; H P Steffens; N K Grzimek; S Schmalz; M J Reddehase
Journal:  J Virol       Date:  1999-01       Impact factor: 5.103

6.  Cytomegalovirus infection in critically ill patients: associated factors and consequences.

Authors:  Samir Jaber; Gérald Chanques; Jean Borry; Bruno Souche; Régis Verdier; Pierre-François Perrigault; Jean-Jacques Eledjam
Journal:  Chest       Date:  2005-01       Impact factor: 9.410

7.  Human cytomegalovirus infections in nonimmunosuppressed critically ill patients.

Authors:  A Heininger; G Jahn; C Engel ; T Notheisen; K Unertl; K Hamprecht
Journal:  Crit Care Med       Date:  2001-03       Impact factor: 7.598

8.  Murine cytomegalovirus infection-induced polyclonal B cell activation is independent of CD4+ T cells and CD40.

Authors:  G Karupiah; T E Sacks; D M Klinman; T N Fredrickson; J W Hartley; J H Chen; H C Morse
Journal:  Virology       Date:  1998-01-05       Impact factor: 3.616

9.  Cmv1-independent antiviral role of NK cells revealed in murine cytomegalovirus-infected New Zealand White mice.

Authors:  Marisela Rodriguez; Pearl Sabastian; Patricia Clark; Michael G Brown
Journal:  J Immunol       Date:  2004-11-15       Impact factor: 5.422

10.  Occult herpes family viruses may increase mortality in critically ill surgical patients.

Authors:  C H Cook; J K Yenchar; T O Kraner; E A Davies; R M Ferguson
Journal:  Am J Surg       Date:  1998-10       Impact factor: 2.565

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  3 in total

1.  Increased morbidity and mortality in murine cytomegalovirus-infected mice following allogeneic bone marrow transplant is associated with reduced surface decay accelerating factor expression.

Authors:  I S El-Amouri; M Bani-Ahmad; Y Tang-Feldman; F Lin; C Ko; C Pomeroy; O R Oakley
Journal:  Clin Exp Immunol       Date:  2010-09-14       Impact factor: 4.330

2.  CD28/B7-mediated co-stimulation is critical for early control of murine cytomegalovirus infection.

Authors:  Charles H Cook; Li Chen; Jin Wen; Peter Zimmerman; Yingxue Zhang; Joanne Trgovcich; Yang Liu; Jian-Xin Gao
Journal:  Viral Immunol       Date:  2009-04       Impact factor: 2.257

3.  Allogeneic stimulation causes transcriptional reactivation of latent murine cytomegalovirus.

Authors:  M R Forster; A A Bickerstaff; J-J Wang; P D Zimmerman; C H Cook
Journal:  Transplant Proc       Date:  2009-06       Impact factor: 1.066

  3 in total

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