Priming with tat-deleted caprine arthritis encephalitis virus (CAEV) proviral DNA or live virus protects goats from challenge with pathogenic CAEV

被引:20
作者
Harmache, A
Vitu, C
Guiguen, F
Russo, P
Bertoni, G
Pepin, M
Vigne, R
Suzan, M
机构
[1] INSERM U372, F-13276 Marseille 09, France
[2] CNEVA Sophia Antipolis, F-06902 Sophia Antipolis, France
[3] Ecole Vet Lyon, Lab Associe INRA ENV, F-69280 Marcy Etoile, France
[4] Univ Bern, Inst Vet Virol, CH-3012 Bern, Switzerland
关键词
D O I
10.1128/JVI.72.8.6796-6804.1998
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
We previously reported that infection of goats with caprine arthritis encephalitis virus (CAEV) tat- proviral DNA or virus results in persistent infection, since the animals seroconverted and direct virus isolation from cultures of blood derived macrophages was positive. In this study we wanted to determine whether goats injected with CAEV tat- proviral DNA or virus were protected against challenge with the pathogenic homologous virus and to investigate whether CAEV tat- was still pathogenic. All animals injected with CAEV tat- became infected as indicated by seroconversion and virus isolation. Challenge at 8 or 9 months postinfection demonstrated protection in four of four animals injected with CAEV tat- but did not in three of three mock-inoculated challenged goats. Challenge virus was undetectable in the blood macrophages of protected animals during a period of 6 or 10 months postchallenge. In two of four protected animals, however, we were able to detect the challenge wild-type virus by reverse transcriptase PCR on RNA directly extracted from synovial membrane cells surrounding the inoculation site. This result suggests that protection was achieved without complete sterilizing immunity. Animals injected with CAEV tat- and mock challenged developed inflammatory lesions in the joints, although these lesions were not as severe as those in CAEV wild-type-injected goats. These results confirm the dispensable role of Tat in CAEV replication in vivo for the establishment of infection and pathogenesis and demonstrate in another lentivirus infection model the efficacy of live attenuated viruses to induce resistance to superinfection.
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页码:6796 / 6804
页数:9
相关论文
共 46 条
[1]   ANTIBODY REACTIVITY TO THE IMMUNODOMINANT EPITOPES OF THE CAPRINE ARTHRITIS-ENCEPHALITIS VIRUS GP38 TRANSMEMBRANE PROTEIN ASSOCIATES WITH THE DEVELOPMENT OF ARTHRITIS [J].
BERTONI, G ;
ZAHNO, ML ;
ZANONI, R ;
VOGT, HR ;
PETERHANS, E ;
RUFF, G ;
CHEEVERS, WP ;
SONIGO, P ;
PANCINO, G .
JOURNAL OF VIROLOGY, 1994, 68 (11) :7139-7147
[2]  
CHEEVERS WP, 1988, LAB INVEST, V58, P510
[3]   Type 1 and type 2 cytokine gene expression by viral gp135 surface protein-activated T lymphocytes in caprine arthritis-encephalitis lentivirus infection [J].
Cheevers, WP ;
Beyer, JC ;
Knowles, DP .
JOURNAL OF VIROLOGY, 1997, 71 (08) :6259-6263
[4]   CROSS-PROTECTIVE IMMUNE-RESPONSES INDUCED IN RHESUS MACAQUES BY IMMUNIZATION WITH ATTENUATED MACROPHAGE-TROPIC SIMIAN IMMUNODEFICIENCY VIRUS [J].
CLEMENTS, JE ;
MONTELARO, RC ;
ZINK, MC ;
AMEDEE, AM ;
MILLER, S ;
TRICHEL, AM ;
JAGERSKI, B ;
HAUER, D ;
MARTIN, LN ;
BOHM, RP ;
MURPHEYCORB, M .
JOURNAL OF VIROLOGY, 1995, 69 (05) :2737-2744
[5]   Evolution of envelope-specific antibody responses in monkeys experimentally infected or immunized with simian immunodeficiency virus and its association with the development of protective immunity [J].
Cole, KS ;
Rowles, JL ;
Jagerski, BA ;
MurpheyCorb, M ;
Unangst, T ;
Clements, JE ;
Robinson, J ;
Wyand, MS ;
Desrosiers, RC ;
Montelaro, RC .
JOURNAL OF VIROLOGY, 1997, 71 (07) :5069-5079
[6]   Macaques infected with live attenuated SIVmac are protected against superinfection via the rectal mucosa [J].
Cranage, MP ;
Whatmore, AM ;
Sharpe, SA ;
Cook, N ;
Polyanskaya, N ;
Leech, S ;
Smith, JD ;
Rud, EW ;
Dennis, MJ ;
Hall, GA .
VIROLOGY, 1997, 229 (01) :143-154
[7]   PROTECTIVE EFFECTS OF A LIVE ATTENUATED SIV VACCINE WITH A DELETION IN THE NEF GENE [J].
DANIEL, MD ;
KIRCHHOFF, F ;
CZAJAK, SC ;
SEHGAL, PK ;
DESROSIERS, RC .
SCIENCE, 1992, 258 (5090) :1938-1941
[8]   TROPISM OF SHEEP LENTIVIRUSES FOR MONOCYTES - SUSCEPTIBILITY TO INFECTION AND VIRUS GENE-EXPRESSION INCREASE DURING MATURATION OF MONOCYTES TO MACROPHAGES [J].
GENDELMAN, HE ;
NARAYAN, O ;
KENNEDYSTOSKOPF, S ;
KENNEDY, PGE ;
GHOTBI, Z ;
CLEMENTS, JE ;
STANLEY, J ;
PEZESHKPOUR, G .
JOURNAL OF VIROLOGY, 1986, 58 (01) :67-74
[9]   SLOW, PERSISTENT REPLICATION OF LENTIVIRUSES - ROLE OF TISSUE MACROPHAGES AND MACROPHAGE PRECURSORS IN BONE-MARROW [J].
GENDELMAN, HE ;
NARAYAN, O ;
MOLINEAUX, S ;
CLEMENTS, JE ;
GHOTBI, Z .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1985, 82 (20) :7086-7090
[10]   OVINE LENTIVIRUS IS MACROPHAGETROPIC AND DOES NOT REPLICATE PRODUCTIVELY IN LYMPHOCYTES-T [J].
GORRELL, MD ;
BRANDON, MR ;
SHEFFER, D ;
ADAMS, RJ ;
NARAYAN, O .
JOURNAL OF VIROLOGY, 1992, 66 (05) :2679-2688