Das S, Marcantonio N, Deponte K, Telford S R, Anderson J F, Kantor F S, Fikrig E
Department of Internal Medicine, Yale University School of Medicine, New Haven, Connecticut 06520-8031, USA.
Am J Trop Med Hyg. 2000 Jan;62(1):99-105. doi: 10.4269/ajtmh.2000.62.99.
Guinea pigs infested with Ixodes scapularis acquire antibody-mediated resistance to tick bites, a phenomenon known as tick-immunity. An I. scapularis salivary gland cDNA expression library was therefore probed with sera from tick-immune guinea pigs to identify antigens that elicit humoral responses in the host. Sera from sensitized guinea pigs strongly recognized 3 of 4,500 library clones in an initial screening. The open reading frames of all 3 clones encoded a putative 16.4-kD acidic protein, designated Salp16, with an N-terminal signal sequence and signal peptidase cleavage sites specific for secretory proteins. The salp16 mRNA and Salp16 protein were detected in the salivary glands of engorged, but not unfed, nymphal and adult ticks, and Salp16 was also found in the saliva of engorged ticks. Immunization with recombinant Salp16 induced high antibody titers in guinea pigs, but did not elicit tick-immunity. Salp16 is the first feeding inducible gene that has been cloned from L. scapularis. Molecular characterization of I. scapularis salivary antigens that are induced upon tick feeding should help to facilitate our understanding of tick-host interactions.
感染肩突硬蜱的豚鼠会产生抗体介导的对蜱叮咬的抗性,这一现象被称为蜱免疫。因此,用来自蜱免疫豚鼠的血清对肩突硬蜱唾液腺cDNA表达文库进行筛选,以鉴定能在宿主体内引发体液免疫反应的抗原。在初步筛选中,来自致敏豚鼠的血清强烈识别了4500个文库克隆中的3个。所有3个克隆的开放阅读框都编码一种假定的16.4-kD酸性蛋白,命名为Salp16,其N端有信号序列和分泌蛋白特有的信号肽酶切割位点。在饱血的若蜱和成蜱的唾液腺中检测到了salp16 mRNA和Salp16蛋白,但未进食的若蜱和成蜱中未检测到,并且在饱血蜱的唾液中也发现了Salp16。用重组Salp16免疫可在豚鼠中诱导产生高抗体滴度,但未引发蜱免疫。Salp16是第一个从肩突硬蜱中克隆的取食诱导基因。对蜱取食时诱导产生的肩突硬蜱唾液抗原进行分子特征分析,应有助于促进我们对蜱-宿主相互作用的理解。