Crother Timothy R, Champion Cheryl I, Whitelegge Julian P, Aguilera Rodrigo, Wu Xiao-Yang, Blanco David R, Miller James N, Lovett Michael A
Department of Medicine, Division of Infectious Diseases, University of California, Los Angeles, 37-121 Center for Health Sciences, 10833 LeConte Ave., Los Angeles, CA 90095, USA.
Infect Immun. 2004 Sep;72(9):5063-72. doi: 10.1128/IAI.72.9.5063-5072.2004.
The numbers of host-adapted Borrelia burgdorferi (HAB) organisms in rabbit skin were assessed by real-time PCR over the first 3 weeks of infection. Maximal numbers were found at day 11, while spirochete numbers decreased by more than 30-fold by day 21. The antigenic composition of HAB in skin biopsy samples was determined by use of a procedure termed hydrophobic antigen tissue Triton extraction. Immune sera from rabbits, sera from chronically infected mice, and monospecific antiserum to the antigenic variation protein, VlsE, were used to probe parallel two-dimensional immunoblots representing each time point. Individual proteins were identified using either specific antisera or by matching protein spots to mass spectrometry-identified protein spots from in vitro-cultivated Borrelia. There were significant changes in the relative expression of a variety of known and previously unrecognized HAB antigens during the 21-day period. OspC and the outer membrane proteins OspA and OspB were prominent at the earliest time point, day 5, when the antigenic variation protein VlsE was barely detected. OspA and OspB were not detected after day 5. OspC was not detected after day 9. VlsE was the most prominent antigen from day 7 through day 21. BmpA, ErpN, ErpP, LA7, OppA-2, DbpA, and an unidentified 15-kDa protein were also detected from day 7 through day 21. Immunoblot analysis using monospecific anti-VlsE revealed the presence of prominent distinct VlsE lower forms in HAB at days 9, 11, and 14; however, these lower forms were no longer detected at day 21. This marked diminution in VlsE lower forms paralleled the clearance of the spirochete from skin.
在感染的前三周,通过实时PCR评估兔皮肤中适应宿主的伯氏疏螺旋体(HAB)生物体数量。在第11天发现数量最多,而到第21天螺旋体数量减少了30倍以上。皮肤活检样本中HAB的抗原组成通过一种称为疏水抗原组织Triton提取的方法来确定。使用来自兔子的免疫血清、慢性感染小鼠的血清以及针对抗原变异蛋白VlsE的单特异性抗血清,对代表每个时间点的平行二维免疫印迹进行检测。使用特异性抗血清或通过将蛋白质斑点与体外培养的伯氏疏螺旋体经质谱鉴定的蛋白质斑点进行匹配来鉴定单个蛋白质。在这21天期间,多种已知和先前未识别的HAB抗原的相对表达发生了显著变化。最早在第5天,OspC以及外膜蛋白OspA和OspB很突出,此时几乎检测不到抗原变异蛋白VlsE。第5天后未检测到OspA和OspB。第9天后未检测到OspC。从第7天到第21天,VlsE是最突出的抗原。从第7天到第21天还检测到了BmpA、ErpN、ErpP、LA7、OppA - 2、DbpA和一种未鉴定的15 kDa蛋白质。使用单特异性抗VlsE的免疫印迹分析显示,在第9天、11天和14天的HAB中存在明显不同的VlsE低分子量形式;然而,在第21天不再检测到这些低分子量形式。VlsE低分子量形式的这种显著减少与螺旋体从皮肤中的清除情况平行。