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首页> 外文期刊>Clinical and vaccine immunology: CVI >Recombinant PorA, the major outer membrane protein of Campylobacter jejuni, provides heterologous protection in an adult mouse intestinal colonization model.
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Recombinant PorA, the major outer membrane protein of Campylobacter jejuni, provides heterologous protection in an adult mouse intestinal colonization model.

机译:重组PorA,主要外膜蛋白空肠弯曲杆菌,提供不同的在成年小鼠肠道保护殖民模型。

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摘要

Immunity against Campylobacter jejuni, a major food-borne pathogen causing diarrhea, is largely serotype specific. The major outer membrane protein (MOMP) of C. jejuni, PorA, is a common antigen with the potential to provide broad protection. Adult BALB/c mice were orally immunized with a recombinant glutathione S-transferase (GST) fused to PorA prepared from Campylobacter jejuni C31 (O:6,7) (GST-PorA) combined with a modified heat-labile enterotoxin of Escherichia coli as an adjuvant and later orally challenged with C31 strain or three heterologous strains: 48 (O:19), 75 (O:3), and 111 (O:1,44). Protection from colonization with the challenge organism was studied by fecal screening daily for 9 days. Serum and intestinal lavage fluid antibodies against the vaccine and Sarkosyl-purified MOMP from C31 were measured by using an enzyme-linked immunosorbent assay. The vaccine produced robust antibody responses against both antigens in serum and secretion. Since strain C31 was a poor colonizer, homologous protection could not be studied. The protective efficacies of heterologous strains were 43% (for strain 48, P < 0.001), 29% (for strain 75, P < 0.005), and 42% (for strain 111, P < 0.001) for the 9-day period compared to control mice given phosphate-buffered saline. Thus, PorA provided appreciable protection against colonization with heterologous serotypes.
机译:主要对空肠弯曲杆菌免疫食源性病原体引起腹泻,主要是特定血清型。蛋白质(MOMP) c .空肠PorA,是一种常见的抗原与提供广泛的潜力保护。谷胱甘肽重组免疫S-transferase(销售税)融合PorA准备空肠弯曲杆菌C31 (O: 6、7)(GST-PorA)结合修改heat-labile肠毒素大肠杆菌作为辅助口头C31应变三个挑战不同的菌株:48 (O: 19), 75 (O: 3),111 (O: 1、44)。粪便生物研究的挑战检查每日9天。灌洗液对疫苗和抗体Sarkosyl-purified MOMP C31的衡量使用酶联免疫吸附试验。疫苗生产强劲的抗体反应对抗原的血清和分泌。从应变C31是个穷殖民者,同源不能保护研究。(功效不同的菌株的43%应变48,P < 0.001), 29%(75株,P <0.005)和42%(111株,P < 0.001)为期九天的时期相比,控制老鼠磷酸盐。明显的保护殖民不同的血清型。

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