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Mechanism of antigenic variation in Mycoplasma pulmonis: interwoven, site-specific DNA inversions.肺炎支原体抗原变异机制:交织的位点特异性DNA倒位
Mol Microbiol. 1995 Nov;18(4):703-14. doi: 10.1111/j.1365-2958.1995.mmi_18040703.x.
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Size and genomic location of the pMGA multigene family of Mycoplasma gallisepticum.鸡毒支原体pMGA多基因家族的大小及基因组定位
Microbiology (Reading). 1996 Jun;142 ( Pt 6):1429-1435. doi: 10.1099/13500872-142-6-1429.
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Expression studies on four members of the pMGA multigene family in Mycoplasma gallisepticum S6.鸡毒支原体S6株中pMGA多基因家族四个成员的表达研究
Microbiology (Reading). 1995 Nov;141 ( Pt 11):3005-14. doi: 10.1099/13500872-141-11-3005.
4
Molecular cloning of a member of the gene family that encodes pMGA, a hemagglutinin of Mycoplasma gallisepticum.编码鸡毒支原体血凝素pMGA的基因家族成员的分子克隆。
Infect Immun. 1993 Mar;61(3):903-9. doi: 10.1128/iai.61.3.903-909.1993.
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Regulation of a restriction and modification system via DNA inversion in Mycoplasma pulmonis.通过肺炎支原体中的DNA倒位对限制与修饰系统进行调控。
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The organisation of the multigene family which encodes the major cell surface protein, pMGA, of Mycoplasma gallisepticum.编码鸡毒支原体主要细胞表面蛋白pMGA的多基因家族的组织方式。
FEBS Lett. 1994 Oct 3;352(3):347-52. doi: 10.1016/0014-5793(94)00991-0.
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鸡毒支原体pMGA基因家族的两个成员的表达呈振荡变化,且受pMGA特异性抗体的影响。

Expression of two members of the pMGA gene family of Mycoplasma gallisepticum oscillates and is influenced by pMGA-specific antibodies.

作者信息

Markham P F, Glew M D, Browning G F, Whithear K G, Walker I D

机构信息

Department of Veterinary Science, The University of Melbourne, Parkville, Victoria, Australia 3052.

出版信息

Infect Immun. 1998 Jun;66(6):2845-53. doi: 10.1128/IAI.66.6.2845-2853.1998.

DOI:10.1128/IAI.66.6.2845-2853.1998
PMID:9596758
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC108280/
Abstract

Certain monoclonal antibodies and polyclonal antisera directed to pMGA, the major protein of Mycoplasma gallisepticum, were tested for the ability to influence the surface phenotype of the cell population which resulted from their inclusion in growth medium. The polyclonal antiserum and one monoclonal antibody (MAb 66) resulted in an alteration of surface phenotype; specifically, populations of cells grown either on plates or in broth cultures which contained these reagents ceased the expression of pMGA and instead expressed an antigenically unrelated new polypeptide (p82). Upon the removal of antibody, the progeny of these cells regained pMGA expression and produced antigenically sectored colonies. The basis of this switch between pMGA+ and pMGA- states was shown to be transcriptional. The p82 polypeptide, the expression of which resulted from growth of cells in antibodies, was another member of the pMGA gene family and was located just downstream from the pMGA gene normally expressed by the M. gallisepticum cells used. Collectively the results of this work suggest that this organism has evolved an unusual means of altering the antigenic composition of its surface in response to antibodies or to other environmental cues.

摘要

针对鸡毒支原体主要蛋白pMGA的某些单克隆抗体和多克隆抗血清,被检测其加入生长培养基后影响细胞群体表面表型的能力。多克隆抗血清和一种单克隆抗体(单克隆抗体66)导致了表面表型的改变;具体而言,在含有这些试剂的平板或肉汤培养物中生长的细胞群体停止表达pMGA,转而表达一种抗原性无关的新多肽(p82)。去除抗体后,这些细胞的后代恢复了pMGA表达,并产生了抗原性扇形菌落。pMGA+和pMGA-状态之间这种转换的基础被证明是转录性的。p82多肽是pMGA基因家族的另一个成员,其表达是细胞在抗体中生长的结果,位于所用鸡毒支原体细胞正常表达的pMGA基因下游。这项工作的结果共同表明,这种生物体进化出了一种不同寻常的方式,以响应抗体或其他环境信号来改变其表面的抗原组成。