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Primary infection protects pigs against re-infection with Lawsonia intracellularis in experimental challenge studies

机译:在实验攻击研究中,原发感染保护猪免于细胞内劳森菌的再感染

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摘要

In two separate trials previous termpigsnext term were experimentally infected with previous termLawsonia intracellularisnext term at 5–6 weeks of age followed by antibiotic treatment and resolution of the previous termprimary infection and then renext term-inoculated at 12–13 weeks of age. A treatment-control group of previous termpigsnext term received the previous termprimary infectionnext term and antibiotic treatment only, and served as control for the antibiotic treatment of the previous termprimary infection.next term A previous termchallengenext term-control group of previous termpigsnext term received the second inoculation dose only at 12–13 weeks of age to control infectivity of the previous termchallengenext term-dose and susceptibility of previous termpigsnext term to L. previous termintracellularisnext term at this age. previous termPigsnext term were monitored for shedding of L. previous termintracellularisnext term in faeces by PCR, and for the development of antibodies and responses of acute phase proteins in serum. The presence of L. previous termintracellularisnext term antigen in the intestinal mucosa was examined in post mortem samples by immunohistochemistry. In both trials previous termprimarynext term infected previous termpigsnext term were protected from previous terminfectionnext term after previous termchallengenext term inoculation as evidenced by absence of faecal shedding of L. previous termintracellularisnext term, lack of changes in acute phase protein concentrations after previous termchallengenext term and with low levels of bacterial antigen in the intestinal mucosa of previous termrenext term-inoculated previous termpigsnext term comparable to that of the treatment-control previous termpigs.next term In contrast, previous termchallengenext term-control previous termpigsnext term shed L. previous termintracellularisnext term in faeces, had L. previous termintracellularisnext term antigen extensively present within all layers of the intestinal mucosa and developed a significant acute phase protein response in serum after the previous termexperimental infection.next term The acute phase protein response to L. previous termintracellularis infectionnext term was detected as an increased rise in the serum concentrations of C-reactive protein and haptoglobin from day-6 post previous terminfection,next term and increased serum concentrations of haptoglobin were generally seen 2–3 weeks after inoculation both at 5–6 and 12–13 weeks of age. In conclusion substantial protection previous termagainstnext term L. previous termintracellularis infectionnext term was found in the previous termrenext term-inoculated previous termpigsnext term in contrast to the development of previous terminfectionnext term in age-matched control previous termpigs.next term The acute phase protein responses reflected both the observed protection previous termagainstnext term L. previous termintracellularis infectionnext term upon secondary previous termchallengenext term and that increased resistance to the previous terminfectionnext term develops with age.
机译:在两项单独的试验中,前一个termpigsnext子项在5-6周龄被实验性感染了上一个termLawsonia细胞内isnext子项,然后进行抗生素治疗并解决了先前的原发性感染,然后在12-13周龄时再次接种renext。上一个白猪前期的治疗对照组仅接受下一个原发感染和下一次抗生素治疗,并作为上一个原发性感染的抗生素治疗的对照组。下一个上一个白猪下一个前期的termchallengenext术语对照组接受了第二个仅在12-13周龄时接种疫苗剂量,以控制该年龄的前termchallengenext术语的剂量和前termpigsnext术语对L. L的敏感性。通过PCR监测Pigsnext术语在粪便中的L.pretermincellularisnext术语的脱落,以及抗体的产生和血清中急性期蛋白的应答。通过免疫组织化学检查死后样品中肠粘膜中L.pretermintracellularisnextterm抗原的存在。在这两个试验中,先前的一期初次下期感染前一期猪以后的一期疫苗均受到保护,以防止前一期次接种后的下一期感染。如前一期细胞内下期粪便没有脱落,上一期远期后急性期蛋白浓度缺乏变化且低上一词的前期肠粘膜中细菌抗原水平接种的前一词的前期与治疗对照的上一词的肠道前期相当。下一个相比之下,上一词的前期对照控制的上一头猪的下一期脱落了粪便中的前一词胞内下一个词,上一期实验性感染后,肠道粘膜各层广泛存在L.先前的termintracellularisnextterm抗原,并在血清中产生了显着的急性期蛋白反应。从上次感染后第6天开始检测到ellularis感染,这是因为C反应蛋白和触珠蛋白的血清浓度升高,从下一次感染后第6天开始,通常在接种后2-3周,下一次和触珠蛋白的血清浓度升高和12-13周龄。综上所述,与在年龄匹配的对照前期猪中发展前期感染后相比,在前期肾期中接种了前期猪的前期中发现了对前期细胞的进一步保护。在继发的先前termchallengenext术语之后观察到的对先前termterminextterm的保护对L. Previoustermincellularis感染nextterm以及随着年龄的增长,对先前termin感染nextterm的抗性增加。

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