Global suppression of mitogen-activated ovine peripheral blood mononuclear cells by surface protein activity from Mycoplasma ovipneumoniae
被引:13
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作者:
Shahzad, W.
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Iowa State Univ, Coll Vet Med, Dept Vet Microbiol & Prevent Med, Ames, IA 50011 USA
Univ Vet & Anim Sci, Dept Clin Med, Lahore, PakistanIowa State Univ, Coll Vet Med, Dept Vet Microbiol & Prevent Med, Ames, IA 50011 USA
Shahzad, W.
[1
,2
]
Ajuwape, Adebowale Titilayo Phillip
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Iowa State Univ, Coll Vet Med, Dept Vet Microbiol & Prevent Med, Ames, IA 50011 USA
Univ Ibadan, Dept Vet Microbiol & Parasitol, Ibadan, NigeriaIowa State Univ, Coll Vet Med, Dept Vet Microbiol & Prevent Med, Ames, IA 50011 USA
Ajuwape, Adebowale Titilayo Phillip
[1
,3
]
Rosenbusch, Ricardo Francisco
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Iowa State Univ, Coll Vet Med, Dept Vet Microbiol & Prevent Med, Ames, IA 50011 USAIowa State Univ, Coll Vet Med, Dept Vet Microbiol & Prevent Med, Ames, IA 50011 USA
Rosenbusch, Ricardo Francisco
[1
]
机构:
[1] Iowa State Univ, Coll Vet Med, Dept Vet Microbiol & Prevent Med, Ames, IA 50011 USA
Mycoplasma ovipneumoniae is associated with chronic non-progressive pneumonia of sheep and goats. As with many other mycoplasmas involved in animal diseases, protective immune responses have not been achieved with vaccines, even though antibody responses can be obtained. This study focuses on characterizing the interaction of M. ovipneumoniae with ovine PBMC using carboxy-fluorescein-succinimidyl-ester (CFSE) loading and flow cytometry to measure lymphoid cell division. M. ovipneumoniae induced a strong in vitro polyclonal suppression of CD4(+), CD8(+), and B blood lymphocyte subsets. The suppressive activity could be destroyed by heating to 60 degrees C. and partially impaired by formalin and binary ethyleneimine treatment that abolished its viability. The activity resided on the surface-exposed membrane protein fraction of the mycoplasma, since mild trypsin treatment: not affecting viability was shown to reduce suppressive activity. Trypsin-treated mycoplasma regained suppressive activity once the mycoplasma was allowed to re-synthesize its surface proteins. Implications for the design of vaccines against M. ovipneumoniae are discussed. (C) 2010 Elsevier B.V. All rights reserved.
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Tel Aviv Univ, Sackler Fac Med, Tel Aviv Sourasky Med Ctr, Dept Pathol, IL-64239 Tel Aviv, IsraelTel Aviv Univ, Sackler Fac Med, Tel Aviv Sourasky Med Ctr, Dept Pathol, IL-64239 Tel Aviv, Israel
Eisenthal, Avi
Eytan, Karin
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Tel Aviv Univ, Sackler Fac Med, Tel Aviv Sourasky Med Ctr, Dept Surg A, IL-64239 Tel Aviv, IsraelTel Aviv Univ, Sackler Fac Med, Tel Aviv Sourasky Med Ctr, Dept Pathol, IL-64239 Tel Aviv, Israel
Eytan, Karin
Brazowski, Eli
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Tel Aviv Univ, Sackler Fac Med, Tel Aviv Sourasky Med Ctr, Dept Pathol, IL-64239 Tel Aviv, IsraelTel Aviv Univ, Sackler Fac Med, Tel Aviv Sourasky Med Ctr, Dept Pathol, IL-64239 Tel Aviv, Israel
Brazowski, Eli
Katz, Ben-Zion
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Tel Aviv Univ, Sackler Fac Med, Tel Aviv Sourasky Med Ctr, Inst Hematol, IL-64239 Tel Aviv, IsraelTel Aviv Univ, Sackler Fac Med, Tel Aviv Sourasky Med Ctr, Dept Pathol, IL-64239 Tel Aviv, Israel
Katz, Ben-Zion
Shirazi, Idit
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Tel Aviv Univ, Sackler Fac Med, Tel Aviv Sourasky Med Ctr, Dept Dermatol, IL-64239 Tel Aviv, IsraelTel Aviv Univ, Sackler Fac Med, Tel Aviv Sourasky Med Ctr, Dept Pathol, IL-64239 Tel Aviv, Israel
Shirazi, Idit
Skornick, Yehuda
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Tel Aviv Univ, Sackler Fac Med, Tel Aviv Sourasky Med Ctr, Dept Surg A, IL-64239 Tel Aviv, IsraelTel Aviv Univ, Sackler Fac Med, Tel Aviv Sourasky Med Ctr, Dept Pathol, IL-64239 Tel Aviv, Israel