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Immunoprotective response induced by recombinant glycoprotein D in the BALB/c respiratory mouse model of Equid alphaherpesvirus 1 infection
被引:2
作者:
Fuentealba, Nadia A.
[1
,4
]
Sguazza, Guillermo H.
[1
]
Zanuzzi, Carolina N.
[2
,4
]
Bravi, Maria E.
[1
,4
]
Scrochi, Mariela R.
[1
,2
,4
]
Valera, Alejandro R.
[1
]
Corva, Santiago G.
[3
]
Gimeno, Eduardo J.
[4
]
Pecoraro, Marcelo R.
[1
]
Galosi, Cecilia M.
[1
,5
]
机构:
[1] Natl Univ La Plata, Dept Virol, Fac Vet Sci, 60 & 118,POB 296, RA-1900 La Plata, Buenos Aires, Argentina
[2] Natl Univ La Plata, Histol & Embryol, Fac Vet Sci, 60 & 118,POB 296, RA-1900 La Plata, Buenos Aires, Argentina
[3] Natl Univ La Plata, Epidemiol, Fac Vet Sci, 60 & 118,POB 296, RA-1900 La Plata, Buenos Aires, Argentina
[4] Natl Res Council CCT CONICET La Plata, Buenos Aires, DF, Argentina
[5] Sci Res Commiss Buenos Aires Prov CIC PBA, Buenos Aires, DF, Argentina
来源:
REVISTA ARGENTINA DE MICROBIOLOGIA
|
2019年
/
51卷
/
02期
关键词:
Equid alphaherpesvirus 1;
Glycoprotein D;
Mouse respiratory model;
EQUINE HERPESVIRUS-1;
IMMUNE-RESPONSES;
TYPE-1;
EHV-1;
VIRUS;
MICE;
VACCINATION;
CHALLENGE;
ANTIBODY;
STRAINS;
MARES;
D O I:
10.1016/j.ram.2018.05.004
中图分类号:
Q93 [微生物学];
学科分类号:
071005 ;
100705 ;
摘要:
Equid alphaherpesvirus 1 (EHV-1) infection causes abortion, respiratory disease, perinatal deaths and neurological disorders in horses. The natural infection and available vaccines provide only partial and short-lived protection against reinfections. In the present study, we analyzed the ability of purified baculovirus-expressed glycoprotein D (gD) administered by different routes to induce protective immunity in BALB/c mice after challenge with the EHV-1 AR8 strain. Clinical signs varied among the different groups of mice immunized by parenteral routes, and, although gD induced a specific serum IgG response, it did not prevent the virus from reaching the lungs. Intranasally immunized mice showed no clinical signs, and virus isolation from lungs, histological lesions and antigen detection by immunohistochemistry were negative. In addition, by this route, gD did not stimulate the production of serum IgG and IgA. However, a specific IgA response in the respiratory tract was confirmed in intranasally immunized mice. Thus, we conclude that the mucosal immune response could reduce the initial viral attachment and prevent the virus from reaching the lungs. Our findings provide additional data to further study new immunization strategies in the natural host. (C) 2018 Asociacion Argentina de Microbiologia. Published by Elsevier Espana, S.L.U.
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页码:119 / 129
页数:11
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