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Host Immune Status Influences the Development of Attaching and Effacing Lesions in Weaned Pigs

机译:宿主免疫状况影响断奶仔猪附着和表皮病变的发展

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摘要

Attaching and effacing Escherichia coli (AEEC) has been associated with naturally occurring attaching and effacing (A/E) lesions in weaned pigs, and although A/E lesions have been experimentally reproduced in newborn piglets, such lesions have been much more difficult to induce in older conventional pigs. Hence, the aim of this study was to examine the effect of oral administration of dexamethasone on the development of A/E lesions in weaned pigs challenged with a porcine enteropathogenic E. coli (PEPEC) strain and to investigate the involvement of local intestinal cytokine response. Dexamethasone, given orally at a dosage of 3 mg kg of body weight−1, significantly enhanced both the colonization of the challenge strain and the prevalence of foci of intimately adherent bacteria, resulting in extensive A/E lesions in the ileum, cecum, and colon of challenged pigs. We also confirmed the expression of both intimin and Tir by PEPEC strain ECL1001 in A/E lesions in vivo, which is, to our knowledge, the first report of the involvement of the latter proteins in any AEEC infections in vivo. Moreover, semiquantitative reverse transcription-PCR demonstrated that interleukin 1β (IL-1β), IL-6, IL-8, and, to a lesser extent, IL-12p40 are significantly upregulated in the ileum following challenge with strain ECL1001, whereas dexamethasone blocks such upregulation. Taken together, our results strongly suggested that host immune status influences the development of A/E lesions in weaned pigs, and it appears that IL-1β, IL-6, IL-8, and, to a lesser extent, IL-12p40 are expressed during infection of weaned pigs by PEPEC and may contribute to the natural resistance of the host against PEPEC infection.
机译:断奶仔猪的附着和脱落大肠杆菌(AEEC)与自然发生的附着和脱落(A / E)损伤有关,尽管新生仔猪已通过实验复制了A / E损伤,但这种损伤很难诱导在较老的常规猪中。因此,本研究的目的是研究地塞米松口服对猪肠致病性大肠杆菌(PEPEC)感染的断奶猪A / E病变的发展,并研究局部肠细胞因子反应的参与。以3 mg kg体重 -1 的剂量口服地塞米松,可显着增强攻击菌株的定殖和紧密粘附细菌的发病率,从而导致广泛的A / E病变在受感染猪的回肠,盲肠和结肠中。我们还证实了PEPEC菌株ECL1001在体内A / E病变中同时表达了intimin和Tir,据我们所知,这是后一种蛋白参与任何AEEC体内感染的第一个报道。此外,半定量逆转录PCR证实,在用菌株ECL1001攻击后,回肠中白介素1β(IL-1β),IL-6,IL-8和IL-12p40显着上调,而地塞米松可阻断这样的上调。综上所述,我们的结果强烈表明宿主免疫状态会影响断奶仔猪的A / E病变的发展,并且看来IL-1β,IL-6,IL-8和较小程度的IL-12p40是在PEPEC感染断奶的仔猪中表达,可能有助于宿主抵抗PEPEC感染的天然抗性。

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