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口服表达完整毒素结构黏附素-类毒素融合蛋白(1FaeG-FedF-LTA₂:5LTB)的减毒活大肠杆菌菌株可使仔猪免受肠致病性大肠杆菌(ETEC)感染。

Oral immunization of a live attenuated Escherichia coli strain expressing a holotoxin-structured adhesin-toxoid fusion (1FaeG-FedF-LTA₂:5LTB) protected young pigs against enterotoxigenic E. coli (ETEC) infection.

机构信息

Veterinary & Biomedical Sciences Department, The Center for Infectious Disease Research & Vaccinology, South Dakota State University, Brookings, SD 57007, USA.

出版信息

Vaccine. 2013 Mar 1;31(11):1458-63. doi: 10.1016/j.vaccine.2013.01.030. Epub 2013 Jan 30.

Abstract

ETEC strains expressing K88 (F4) or F18 fimbriae and enterotoxins are the predominant cause of porcine post-weaning diarrhea (PWD). PWD continues causing significant economic losses to swine producers worldwide. Vaccines effectively protecting against PWD are needed. Our recent study revealed that a tripartite adhesin-toxin monomer (FaeG-FedF-LT(A2-B)) elicited protective antibodies. In this study, we constructed a new adhesin-toxoid fusion, expressed it as a 1A:5B holotoxin-structured antigen (1FaeG-FedF-LT(192A2):5LT(B)) in an avirulent Escherichia coli strain, and evaluated its vaccine potential in pig challenge studies. Piglets orally inoculated with this live strain showed no adverse effects but developed systemic and mucosal antibodies that neutralized cholera toxin and inhibited adherence of K88 and F18 fimbriae in vitro. Moreover, the immunized piglets, when were challenged with ETEC strain 3030-2 (K88ac/LT/STb), had significant fewer bacteria colonized at small intestines and did not develop diarrhea; whereas the control piglets developed severe diarrhea and died. These results indicated the 1FaeG-FedF-LT(192A2):5LT(B) fusion antigen induced protective antiadhesin and antitoxin immunity in pigs, and suggested a live attenuated vaccine can be potentially developed against porcine ETEC diarrhea. Additionally, presenting antigens in a holotoxin structure to target host local mucosal immunity can be used in vaccine development against other enteric diseases.

摘要

表达 K88(F4)或 F18 菌毛和肠毒素的 ETEC 菌株是引起仔猪断奶后腹泻(PWD)的主要原因。PWD 继续给全球养猪生产者造成重大经济损失。需要有效的疫苗来预防 PWD。我们最近的研究表明,三聚体黏附素-毒素单体(FaeG-FedF-LT(A2-B))能激发保护性抗体。在这项研究中,我们构建了一种新的黏附素类毒素融合蛋白,在一种无毒的大肠杆菌菌株中表达为 1A:5B 全毒素结构抗原(1FaeG-FedF-LT(192A2):5LT(B)),并在猪攻毒研究中评估了其疫苗潜力。口服接种该活菌的仔猪没有不良反应,但产生了系统和黏膜抗体,中和霍乱毒素,并抑制 K88 和 F18 菌毛在体外的黏附。此外,用 ETEC 菌株 3030-2(K88ac/LT/STb)攻毒免疫仔猪后,小肠定植的细菌数量显著减少,且未发生腹泻;而对照组仔猪则发生严重腹泻并死亡。这些结果表明,1FaeG-FedF-LT(192A2):5LT(B)融合抗原在猪中诱导了保护性抗黏附素和抗毒素免疫,提示可以开发活减毒疫苗来预防猪 ETEC 腹泻。此外,以全毒素结构呈现抗原以靶向宿主局部黏膜免疫可用于针对其他肠道疾病的疫苗开发。

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