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首页> 外文期刊>BMC Veterinary Research >Dexamethasone treatment did not exacerbate Seneca Valley virus infection in nursery-age pigs
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Dexamethasone treatment did not exacerbate Seneca Valley virus infection in nursery-age pigs

机译:地塞米松治疗没有加剧苗圃猪中塞内卡谷病毒感染

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Senecavirus A, commonly known as Seneca Valley virus (SVV), is a picornavirus that has been infrequently associated with porcine idiopathic vesicular disease (PIVD). In late 2014 there were multiple PIVD outbreaks in several states in Brazil and samples from those cases tested positive for SVV. Beginning in July of 2015, multiple cases of PIVD were reported in the United States in which a genetically similar SVV was also detected. These events suggested SVV could induce vesicular disease, which was recently demonstrated with contemporary US isolates that produced mild disease in pigs. It was hypothesized that stressful conditions may exacerbate the expression of clinical disease and the following experiment was performed. Two groups of 9-week-old pigs were given an intranasal SVV challenge with one group receiving an immunosuppressive dose of dexamethasone prior to challenge. After challenge animals were observed for the development of clinical signs and serum and swabs were collected to study viral shedding and antibody production. In addition, pigs were euthanized 2, 4, 6, 8, and 12?days post inoculation (dpi) to demonstrate tissue distribution of virus during acute infection. Vesicular disease was experimentally induced in both groups with the duration and magnitude of clinical signs similar between groups. During acute infection [0–14?days post infection (dpi)], SVV was detected by PCR in serum, nasal swabs, rectal swabs, various tissues, and in swabs from ruptured vesicles. From 15 to 30 dpi, virus was less consistently detected in nasal and rectal swabs, and absent from most serum samples. Virus neutralizing antibody was detected by 5 dpi and lasted until the end of the study. Treatment with an immunosuppressive dose of dexamethasone did not drastically alter the clinical disease course of SVV in experimentally infected nursery aged swine. A greater understanding of SVV pathogenesis and factors that could exacerbate disease can help the swine industry with control and prevention strategies directed against this virus.
机译:SeNecavirus A,通常称为SeNeca Valley病毒(SVV),是一种富人与猪特性囊泡疾病(PIVD)相关的皮革病毒。 2014年底,巴西的几个州有多种PIVD爆发,来自这些病例的样品对SVV进行了阳性。从2015年7月开始,在美国报告了多种PIVD案例,其中还检测到遗传上类似的SVV。这些事件表明SVV可以诱导凹凸疾病,最近展示了当代美国分离物在猪中产生轻微的疾病。假设压力条件可能加剧临床疾病的表达,并进行以下实验。在攻击之前,给出了两组9周龄猪的鼻内SVV攻击,其中一组接受免疫抑制剂量的地塞米松。在观察到挑战动物以进行临床症状的发展,收集血清和拭子,以研究病毒脱落和抗体产生。此外,猪被安乐死2,4,6,8和12?天后接种(DPI),以证明在急性感染期间病毒的组织分布。在两组中实验诱导脉络疾病,其持续时间和级别在组之间的临床符号。在急性感染期间[0-14〜14天后(DPI)],通过PCR在血清,鼻拭子,直肠拭子,各种组织和来自破裂囊泡的拭子中检测SVV。从15至30 dpi,病毒在鼻腔和直肠拭子中持续持续检测,并且没有大多数血清样品。通过5 dpi检测病毒中和抗体并持续直至研究结束。用免疫抑制剂量的地塞米松治疗并未大大改变实验感染的苗圃猪的SVV临床疾病进程。对SVV发病机制的更大了解,可以加剧疾病的因素可以帮助猪工业进行控制和预防策略针对这种病毒。

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