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牛用双价非精制重组肉毒梭菌疫苗的免疫原性。

Immunogenicity of a Bivalent Non-Purified Recombinant Vaccine against Botulism in Cattle.

机构信息

Centro de Desenvolvimento Tecnológico, Universidade Federal de Pelotas, Pelotas, Rio Grande do Sul 96160-000, Brazil.

Instituto de Medicina Veterinária, Universidade Federal do Pará, Castanhal, Pará 68740-910, Brazil.

出版信息

Toxins (Basel). 2018 Sep 20;10(10):381. doi: 10.3390/toxins10100381.

Abstract

Botulism is a potentially fatal intoxication caused by botulinum neurotoxins (BoNTs) produced mainly by . Vaccination against BoNT serotypes C and D is the main procedure to control cattle botulism. Current vaccines contain formaldehyde-inactivated native BoNTs, which have a time-consuming production process and pose safety risks. The development of non-toxic recombinant vaccines has helped to overcome these limitations. This study aims to evaluate the humoral immune response generated by cattle immunized with non-purified recombinant fragments of BoNTs C and D. Cattle were vaccinated in a two-dose scheme with 100, 200 and 400 µg of each antigen, with serum sampling on days 0, 56, 120, and 180 after vaccination. Animals who received either 200 or 400 μg of both antigens induced titers higher than the minimum required by the Brazilian ministry of Agriculture, Livestock and Food Supply and achieved 100% (8/8) seroconversion rate. Animals vaccinated with commercial toxoid vaccine had only a 75% (6/8) seroconversion rate for both toxins. Animals that received doses containing 400 µg of recombinant protein were the only ones to maintain titers above the required level up until day 120 post-vaccination, and to achieve 100% (8/8) seroconversion for both toxins. In conclusion, 400 µg the recombinant cell lysates supernatant was demonstrated to be an affordable means of producing an effective and safe botulism vaccine for cattle.

摘要

肉毒中毒是由肉毒梭菌神经毒素(BoNTs)引起的潜在致命性中毒,主要由 产生。针对 BoNT 血清型 C 和 D 的疫苗接种是控制牛肉毒中毒的主要程序。目前的疫苗含有甲醛灭活的天然 BoNTs,其生产过程耗时且存在安全风险。无毒重组疫苗的开发有助于克服这些限制。本研究旨在评估用未纯化的 BoNT C 和 D 重组片段免疫牛产生的体液免疫反应。牛以两剂方案接种,每剂接种 100、200 和 400 µg 各抗原,在接种后第 0、56、120 和 180 天采集血清。接受 200 或 400 µg 两种抗原的动物诱导的滴度均高于巴西农业、畜牧业和食品供应部规定的最低要求,达到了 100%(8/8)的血清转化率。接受商业类毒素疫苗接种的动物两种毒素的血清转化率仅为 75%(6/8)。接受含 400 µg 重组蛋白剂量的动物是唯一能够维持接种后 120 天以上所需水平并达到两种毒素 100%(8/8)血清转化率的动物。总之,400 µg 的重组细胞裂解物上清液被证明是生产牛肉毒中毒有效和安全疫苗的一种经济实惠的方法。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0fa7/6215264/8ec198c5c997/toxins-10-00381-g001.jpg

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