Evaluation of two commercially-available Salmonella vaccines on Salmonella in the peripheral lymph nodes of experimentally-infected cattle.

Q2 Medicine
Therapeutic Advances in Vaccines and Immunotherapy Pub Date : 2020-10-05 eCollection Date: 2020-01-01 DOI:10.1177/2515135520957760
Thomas S Edrington, Terrance M Arthur, Guy H Loneragan, Kenneth J Genovese, Devin L Hanson, Robin C Anderson, David J Nisbet
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引用次数: 8

Abstract

Background: Salmonella is a common inhabitant of the ruminant gastrointestinal tract, where it often resides asymptomatically and may be shed into the feces. More recently it was discovered that Salmonella may be contained within the peripheral, non-mesenteric lymph nodes, where it is impervious to in-plant pathogen control interventions and may serve as a source of Salmonella-contamination of ground beef. Over the past 10 years considerable research effort has been expended at understanding how this pathogen gets to these lymph nodes, the duration of infection, and, most importantly, screening and developing potential intervention strategies that may be employed on farm prior to the animal being presented for slaughter.

Methods: Utilizing an experimental model of Salmonella inoculation of bovine peripheral lymph nodes (PLNs), two pilot vaccine experiments were conducted to evaluate two Salmonella vaccines: Salmonella Newport Bacterial Extract (Experiment I) and Endovac-Bovi® (Experiment II) on preventing Salmonella acquisition by these nodes. In Experiment I, 4 months following the booster vaccination, 30 steers were inoculated with three Salmonella serotypes intradermally: Newport, Montevideo, and Anatum administered to the right legs, left legs, and to the caudal thorax and abdomen, respectively. Cattle were inoculated every other day over the course of five days (three total inoculation events) and 6 and 12 days following the final Salmonella inoculation, 16 and 14 head in each treatment were euthanized, respectively. In Experiment II, 12 head of Holstein steers were utilized. Seven days following the booster and weekly thereafter for 3 weeks (four total inoculation events), cattle were inoculated as above and euthanized 7 days following final inoculation. Right and left sub-iliac, popliteal and pre-scapular lymph nodes were collected in each experiment, weighed and cultured for Salmonella.

Results: In Experiment I, no treatment differences were observed in Salmonella prevalence 6 days post-inoculation (necropsy 1). However, in vaccinated cattle at the second necropsy, a reduction (p = 0.05) in Salmonella prevalence was observed in the sub-iliac and pre-scapular lymph nodes as well as when all nodes were evaluated collectively (p = 0.04). In Experiment II, the vaccine reduced (p = 0.03) Salmonella prevalence in the right popliteal and tended (p = 0.09) to decrease prevalence in both popliteal lymph nodes.

Conclusion: Under these experimental conditions, the data generated provide evidence of a partial vaccine effect on Salmonella within PLNs and indicate that further research may be warranted.

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两种市售沙门氏菌疫苗对实验感染牛外周淋巴结沙门氏菌的影响。
背景:沙门氏菌是反刍动物胃肠道中常见的居民,它通常无症状地居住在那里,并可能进入粪便。最近发现,沙门氏菌可能存在于外周、非肠系膜淋巴结中,在那里,它不受植物内病原体控制干预措施的影响,并可能成为碎牛肉沙门氏菌污染的来源。在过去的10年里,人们花费了大量的研究精力来了解这种病原体是如何进入这些淋巴结的,感染的持续时间,最重要的是,在动物被宰杀之前,筛选和制定可能在农场使用的潜在干预策略。方法:采用牛外周淋巴结沙门氏菌接种实验模型,进行两项疫苗试验,评价两种沙门氏菌疫苗:沙门氏菌纽波特菌提取物(实验一)和Endovac-Bovi®(实验二)对外周淋巴结感染沙门氏菌的预防作用。实验一,在加强接种4个月后,30头牛分别皮内接种纽波特、蒙得维的亚和阿纳图姆三种血清型沙门氏菌,分别接种于右腿、左腿和胸腹尾部。在5天(共接种3次)和最后一次沙门氏菌接种后的6天和12天内,每隔一天接种一次牛,分别对16头和14头进行安乐死。试验二选用荷斯坦阉牛12头。在加强剂接种后第7天,此后每周接种一次,共接种4次,共接种3周,按上述方法接种,并在最后接种后第7天对牛实施安乐死。每次实验均收集左右髂下、腘窝和肩胛前淋巴结,称重并培养沙门氏菌。结果:在实验1中,接种后6天(尸检1)沙门氏菌患病率未见处理差异。然而,在第二次尸检时,接种过疫苗的牛,髂下和肩胛前淋巴结以及所有淋巴结的沙门氏菌患病率均有所降低(p = 0.05) (p = 0.04)。在实验二中,疫苗降低了右腘窝的沙门氏菌患病率(p = 0.03),并有降低双腘窝淋巴结患病率的趋势(p = 0.09)。结论:在这些实验条件下,产生的数据提供了疫苗对pln内沙门氏菌部分作用的证据,并表明可能需要进一步研究。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Therapeutic Advances in Vaccines and Immunotherapy
Therapeutic Advances in Vaccines and Immunotherapy Medicine-Pharmacology (medical)
CiteScore
5.10
自引率
0.00%
发文量
15
审稿时长
8 weeks
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