Local ileal cytokine responses in cattle during a primary infection with Cryptosporidium parvum

被引:14
作者
Canals, A [1 ]
Pasquali, P [1 ]
Zarlenga, DS [1 ]
Fayer, R [1 ]
Almeria, S [1 ]
Gasbarre, LC [1 ]
机构
[1] USDA ARS, Immunol & Dis Resistance Lab, BARC E, LPSI, Beltsville, MD 20705 USA
关键词
D O I
10.2307/3284541
中图分类号
R38 [医学寄生虫学]; Q [生物科学];
学科分类号
07 ; 0710 ; 09 ; 100103 ;
摘要
In the present study, localized changes in cytokine transcription profiles were examined in neonatal calves following a primary infection with Cryptosporidium parvum, using competitive reverse transcriptase polymerase chain reaction (RT-PCR). Total RNA was prepared from ileocecal lymph nodes (LN), lamina propria lymphocytes (LPL), and intraepithelial lymphocytes (IEL) isolated from neonatal calves 7 days after C. parvum infection. Competitive RT-PCR performed on cDNA samples containing internal cytokine gene competitor molecules showed increases in the levels of interferon-gamma and interleukin-12 (IL-12) (P40) mRNA in both LPL and IEL populations but not in the draining LN. In addition, the levels of mRNA of the newly identified growth factor IL-15 decreased in the IEL of the infected animals. No consistent differences were seen in any of the cell populations when the samples were analyzed for IL-10 and levels of mRNA for IL-2 and IL-4 were low and highly variable in both infected and control groups in all 3 lymphocyte populations.
引用
收藏
页码:125 / 130
页数:6
相关论文
共 32 条
[1]   Localization of alpha/beta and gamma/delta T lymphocytes in Cryptosporidium parvum-infected tissues in naive and immune calves [J].
Abrahamsen, MS ;
Lancto, CA ;
Walcheck, B ;
Layton, W ;
Jutila, MA .
INFECTION AND IMMUNITY, 1997, 65 (06) :2428-2433
[2]   Isolation and phenotypic characterization of abomasal mucosal lymphocytes in the course of a primary Ostertagia ostertagi infection an calves [J].
Almeria, S ;
Canals, A ;
Zarlenga, DS ;
Gasbarre, LC .
VETERINARY IMMUNOLOGY AND IMMUNOPATHOLOGY, 1997, 57 (1-2) :87-98
[3]   Cytokine profile induced by a primary infection with Ostertagia ostertagi in cattle [J].
Canals, A ;
Zarlenga, DS ;
Almeria, S ;
Gasbarre, LC .
VETERINARY IMMUNOLOGY AND IMMUNOPATHOLOGY, 1997, 58 (01) :63-75
[4]   Cloning and expression of bovine interleukin-15: Analysis and modulation of transcription by exogenous stimulation [J].
Canals, A ;
Gasbarre, LC ;
Boyd, PC ;
Almeria, S ;
Zarlenga, DS .
JOURNAL OF INTERFERON AND CYTOKINE RESEARCH, 1997, 17 (08) :473-480
[5]   REQUIREMENTS FOR CD4+ CELLS AND GAMMA-INTERFERON IN RESOLUTION OF ESTABLISHED CRYPTOSPORIDIUM-PARVUM INFECTION IN MICE [J].
CHEN, WX ;
HARP, JA ;
HARMSEN, AG .
INFECTION AND IMMUNITY, 1993, 61 (09) :3928-3932
[6]   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
[7]   The pathogenesis of cryptosporidiosis [J].
Clark, DP ;
Sears, CL .
PARASITOLOGY TODAY, 1996, 12 (06) :221-225
[8]   Specific interferon-gamma, IgA and IgM responses after experimental infection of neonatal calves with Cryptosporidium parvum [J].
De Graaf, DC ;
Peeters, JE .
INTERNATIONAL JOURNAL FOR PARASITOLOGY, 1997, 27 (01) :131-134
[9]  
ENRIQUEZ FJ, 1993, FOLIA PARASIT, V40, P307
[10]   CRYPTOSPORIDIUM SPP AND CRYPTOSPORIDIOSIS [J].
FAYER, R ;
UNGAR, BLP .
MICROBIOLOGICAL REVIEWS, 1986, 50 (04) :458-483