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Application of median lethal concentration (LC50) of pathogenic microorganisms and their antigens in vaccine development

机译:致病微生物和抗原中位致死浓度(LC50)在疫苗发育中的应用

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摘要

Abstract Objective Lack of ideal mathematical models to qualify and quantify both pathogenicity, and virulence is a dreadful setback in development of new antimicrobials and vaccines against resistance pathogenic microorganisms. Hence, the modified arithmetical formula of Reed and Muench has been integrated with other formulas and used to determine bacterial colony forming unit/viral concentration, virulence and immunogenicity. Results Microorganisms’ antigens tested are Staphylococcus aureus, Streptococcus pneumoniae, Pseudomonas aeruginosa in mice and rat, Edwardsiella ictaluri, Aeromonas hydrophila, Aeromonas veronii in fish, New Castle Disease virus in chicken, Sheep Pox virus, Foot-and-Mouth Disease virus and Hepatitis A virus in vitro, respectively. The LC50s for the pathogens using different routes of administrations are 1.93 × 103(sheep poxvirus) and 1.75 × 1010 for Staphylococcus aureus (ATCC29213) in rat, respectively. Titer index (TI) equals N log10 LC50 and provides protection against lethal dose in graded fashion which translates to protection index. N is the number of vaccine dose that could neutralize the LC50. Hence, parasite inoculum of 103 to 1011 may be used as basis for determination of LC50 and median bacterial concentrations (BC50).Pathogenic dose for immune stimulation should be sought at concentration about LC10.
机译:摘要目的缺乏理想的数学模型,以符合致病性和量化致病性,并且毒力是一种可怕的挫折,在抗性致病病原微生物的新抗微生物和疫苗的发展中。因此,芦苇和麦塞的改性氧化氧化算术已与其他配方结合,并用于确定细菌菌落形成单元/病毒浓度,毒力和免疫原性。结果微生物的抗原测试是金黄色葡萄球菌,肺炎链球菌肺炎群岛,铜绿假单胞菌,埃特氏菌,Aeromonas intraluri,患者肝癌,鸡,羊痘病毒,患有肝炎病毒和肝炎的新城堡疾病病毒。病毒分别在体外。使用不同施用途径的病原体的LC50s分别是大鼠金黄色葡萄球菌(ATCC29213)的1.93×103(绵羊Poxvirus)和1.75×1010。滴度指数(TI)等于N LOG10 LC50,并为渐变时尚的致命剂量提供保护,转化为保护指数。 n是可以中和LC50的疫苗剂量的数量。因此,103至1011的寄生虫接种可以用作测定LC50的基础和中值细菌浓度(BC50)。应在浓度下寻求免疫刺激的Spapocic剂量,浓度约为LC10。

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    Saganuwan Alhaji Saganuwan;

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  • 年度 2020
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  • 原文格式 PDF
  • 正文语种 eng
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