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

被引:48
作者
Henry, SC
Schmader, K
Brown, TT
Miller, SE
Howell, DN
Daley, GG
Hamilton, JD
机构
[1] Dept Vet Affairs, Med Res Serv, Durham, NC 27705 USA
[2] Res Ctr AIDS & HIV Infect, Durham, NC 27705 USA
[3] N Carolina State Univ, Coll Vet Med, Raleigh, NC USA
[4] Duke Univ, Med Ctr, Dept Med, Durham, NC 27710 USA
[5] Duke Univ, Med Ctr, Dept Pathol, Durham, NC 27710 USA
关键词
recombinant cytomegalovirus; green fluorescent protein; cytomegalovirus infection;
D O I
10.1016/S0166-0934(00)00202-0
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
A recombinant murine cytomegalovirus (mCMV) that expresses enhanced green fluorescent protein (EGFP) under control of the native immediate-early 1/3 promoter was constructed to detect directly sites of viral activity in latent and reactivated infections. The recombinant virus had acute and latent infection characteristics similar to those of wild-type mCMV. Rare green-fluorescing foci were observed in paraffin sections from lungs and spleens infected latently. Positive immunoperoxidase staining for EGFP in sections of the same lung tissues suggests that these cells may be sites of restricted viral gene expression. EGFP was detected easily in tissue explants reactivating from latent infection in vitro. Morphology and adhesion characteristics of fluorescing cells suggest that viral reactivation occurs in tissue macrophages in explant cultures. The observations presented in this study demonstrate the usefulness of EGFP-expressing recombinants as tools for direct tracking of mCMV activity in vivo and in vitro. (C) 2000 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:61 / 73
页数:13
相关论文
共 40 条
[1]   LUNGS ARE A MAJOR ORGAN SITE OF CYTOMEGALOVIRUS LATENCY AND RECURRENCE [J].
BALTHESEN, M ;
MESSERLE, M ;
REDDEHASE, MJ .
JOURNAL OF VIROLOGY, 1993, 67 (09) :5360-5366
[2]  
BRITT WJ, 1996, FIELDS VIROLOGY, P2493
[3]   MURINE CYTOMEGALOVIRUS IE2, AN ACTIVATOR OF GENE-EXPRESSION, IS DISPENSABLE FOR GROWTH AND LATENCY IN MICE [J].
CARDIN, RD ;
ABENES, GB ;
STODDART, CA ;
MOCARSKI, ES .
VIROLOGY, 1995, 209 (01) :236-241
[4]   GREEN FLUORESCENT PROTEIN AS A MARKER FOR GENE-EXPRESSION [J].
CHALFIE, M ;
TU, Y ;
EUSKIRCHEN, G ;
WARD, WW ;
PRASHER, DC .
SCIENCE, 1994, 263 (5148) :802-805
[5]   SINGLE-STEP METHOD OF RNA ISOLATION BY ACID GUANIDINIUM THIOCYANATE PHENOL CHLOROFORM EXTRACTION [J].
CHOMCZYNSKI, P ;
SACCHI, N .
ANALYTICAL BIOCHEMISTRY, 1987, 162 (01) :156-159
[6]   DETECTION OF LATENT CYTOMEGALOVIRUS DNA IN DIVERSE ORGANS OF MICE [J].
COLLINS, T ;
POMEROY, C ;
JORDAN, MC .
JOURNAL OF INFECTIOUS DISEASES, 1993, 168 (03) :725-729
[7]   FACS-optimized mutants of the green fluorescent protein (GFP) [J].
Cormack, BP ;
Valdivia, RH ;
Falkow, S .
GENE, 1996, 173 (01) :33-38
[8]   MOLECULAR-CLONING AND PHYSICAL MAPPING OF MURINE CYTOMEGALOVIRUS DNA [J].
EBELING, A ;
KEIL, GM ;
KNUST, E ;
KOSZINOWSKI, UH .
JOURNAL OF VIROLOGY, 1983, 47 (03) :421-433
[9]   Cytomegalovirus remains latent in a common precursor of dendritic and myeloid cells [J].
Hahn, G ;
Jores, R ;
Mocarski, ES .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1998, 95 (07) :3937-3942
[10]   TRANSMISSION OF LATENT CYTOMEGALO-VIRUS IN A MURINE KIDNEY TISSUE-TRANSPLANTATION MODEL [J].
HAMILTON, JD ;
SEAWORTH, BJ .
TRANSPLANTATION, 1985, 39 (03) :290-296