Characterization of the Interferon-α Response of Pigs to the Weaning Stress

被引:14
作者
Razzuoli, Elisabetta [1 ]
Villa, Riccardo [1 ]
Sossi, Enrico [1 ]
Amadori, Massimo [1 ]
机构
[1] IZSLER, Cellular Immunol Lab, I-25124 Brescia, Italy
关键词
MURINE PERITONEAL-MACROPHAGES; INFLAMMATORY RESPONSE; MESSENGER-RNA; IFN-ALPHA; VIRUS; EXPRESSION; CELLS; TRANSCRIPTION; LEUKOCYTES; BACTERIAL;
D O I
10.1089/jir.2010.0041
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The interferon (IFN)-alpha response of pigs to the stressing event of early weaning was investigated in a field trial. All the animals under study remained healthy and tested negative for common viral infections. However, a low-titered IFN-alpha response was detected in many sera by a bioassay on Madin-Darby bovine kidney (MDBK) cells on day +6 after weaning. Porcine IFN-alpha was unambiguously identified by a neutralization assay on a pool of IFN-alpha-positive sera. By gel filtration chromatography, the antiviral activity of sera on MDBK cells could be traced back to 3 components of apparent molecular mass 27/18/ < 14 kDa. Additional components of apparent molecular mass 58 and 41 kDa were revealed by ELISA in Nonidet P-40 lysates of peripheral blood mononuclear cells (PBMC). Also, many pigs tested positive in flow cytometry assays on PBMC for intracellular IFN-alpha. The expression of porcine IFN-alpha genes was investigated by reverse transcriptase (RT) real-time polymerase chain reaction at days -1, +6, and +12 with regard to weaning in PBMC of 9 piglets. On days -1 and +12, IFN A5, A6, A12, as well as (in fewer pigs) A1, A7, A11, and A2 genes were shown to be expressed. On the contrary, none of the above genes was expressed on day +6, when plenty of pig sera were IFN-alpha-positive. Our results indicate that weaning causes the release of IFN-alpha and the transient shut-off of the corresponding gene transcriptions in PBMC. Interestingly, only IFN A9 gene transcription was shown in vitro to be virus induction-dependent.
引用
收藏
页码:237 / 247
页数:11
相关论文
共 50 条
[21]   INDUCTION OF HCV-SPECIFIC CELL RESPONSE IN VITRO BY DENDRITIC CELLS GENERATED WITH INTERFERON-α [J].
Chernykh, E. R. ;
Oleynik, E. A. ;
Leplina, O. Yu ;
Tikhonova, M. A. ;
Tyrinova, T., V ;
Starostina, N. M. ;
Ostanin, A. A. .
INFEKTSIYA I IMMUNITET, 2019, 9 (01) :76-86
[22]   Effects of interferon-α, interferon-γ and cAMP on the transcriptional regulation of the serotonin transporter [J].
Morikawa, O ;
Sakai, N ;
Obara, H ;
Saito, N .
EUROPEAN JOURNAL OF PHARMACOLOGY, 1998, 349 (2-3) :317-324
[23]   Polymorphisms of interferon-λ4 and IL28B - effects on treatment response to interferon/ribavirin in patients with chronic hepatitis C [J].
Staettermayer, A. F. ;
Strassl, R. ;
Maieron, A. ;
Rutter, K. ;
Stauber, R. ;
Strasser, M. ;
Beinhardt, S. ;
Datz, C. ;
Scherzer, T. -M. ;
Steindl-Munda, P. ;
Gschwantler, M. ;
Trauner, M. ;
Hofer, H. ;
Ferenci, P. .
ALIMENTARY PHARMACOLOGY & THERAPEUTICS, 2014, 39 (01) :104-111
[24]   Interferon-β Signaling Contributes to Ras Transformation [J].
Tsai, Yu-Chen ;
Pestka, Sidney ;
Wang, Lu-Hai ;
Runnels, Loren W. ;
Wan, Shan ;
Lyu, Yi Lisa ;
Liu, Leroy F. .
PLOS ONE, 2011, 6 (08)
[25]   Association of the Response to Tumor Necrosis Factor Antagonists With Plasma Type I Interferon Activity and Interferon-β/α Ratios in Rheumatoid Arthritis Patients [J].
Mavragani, Clio P. ;
La, Dan T. ;
Stohl, William ;
Crow, Mary K. .
ARTHRITIS AND RHEUMATISM, 2010, 62 (02) :392-401
[26]   Dihydropyrimidine dehydrogenase predicts survival and response to interferon-α in hepatocellular carcinoma [J].
Zhu, Wei-Ping ;
Liu, Ze-Yang ;
Zhao, Yi-Ming ;
He, Xi-Gan ;
Pan, Qi ;
Zhang, Ning ;
Zhou, Jia-Min ;
Wang, Long-Rong ;
Wang, Miao ;
Zhan, Di-Hua ;
Ma, De-Ning ;
Wang, Lu .
CELL DEATH & DISEASE, 2018, 9
[27]   Human interferon-λ3 is a potent member of the type III interferon family [J].
Dellgren, C. ;
Gad, H. H. ;
Hamming, O. J. ;
Melchjorsen, J. ;
Hartmann, R. .
GENES AND IMMUNITY, 2009, 10 (02) :125-131
[28]   Attenuated expression of interferon-β and interferon-λl by human alternatively activated macrophages [J].
El Fiky, Ashraf ;
Perreault, Roger ;
McGinnis, Gwendolyn J. ;
Rabin, Ronald L. .
HUMAN IMMUNOLOGY, 2013, 74 (12) :1524-1530
[29]   Intrahepatic Transcriptional Signature Associated with Response to Interferon-α Treatment in the Woodchuck Model of Chronic Hepatitis B [J].
Fletcher, Simon P. ;
Chin, Daniel J. ;
Gruenbaum, Lore ;
Bitter, Hans ;
Rasmussen, Erik ;
Ravindran, Palanikumar ;
Swinney, David C. ;
Birzele, Fabian ;
Schmucki, Roland ;
Lorenz, Stefan H. ;
Kopetzki, Erhard ;
Carter, Jade ;
Triyatni, Miriam ;
Thampi, Linta M. ;
Yang, Junming ;
AlDeghaither, Dalal ;
Murredu, Marta G. ;
Cote, Paul ;
Menne, Stephan .
PLOS PATHOGENS, 2015, 11 (09) :1-30
[30]   Expression of type I interferon receptor as a predictor of clinical response to interferon-α therapy of gastrointestinal cancers [J].
Ota, Hideo ;
Nagano, Hiroaki ;
Doki, Yuichiro ;
Sekimoto, Mitsugu ;
Kondo, Motoi ;
Wada, Hiroshi ;
Nakamura, Masato ;
Noda, Takehiro ;
Damdinsuren, Bazarragchaa ;
Marubashi, Shigeru ;
Miyamoto, Atsushi ;
Takeda, Yutaka ;
Dono, Keizo ;
Umeshita, Koji ;
Nakamori, Shoji ;
Wakasa, Kenichi ;
Sakon, Masato ;
Monden, Morito .
ONCOLOGY REPORTS, 2006, 16 (02) :249-255