Exploring the Role of Cathelicidin Antimicrobial Peptide, Toll-Like Receptor 4, and HMGB-1 in Bacterial Infection

Ami Febriza, H. Idrus, V. Kasim
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Abstract

Lipopolysaccharides (LPS) from Salmonella typhi will attach with Toll-Like Receptor 4 (TLR-4) and trigger an inflammatory response to fight the pathogen. Due to infection, the HMGB1 is produced by immune cells or secreted passively from dead cells. Fur-thermore, the antimicrobial peptide, cathelicidin was secreted to neutralize and eliminate these path-ogens. This study aims to examine the interaction of Cathelicidin antimicrobial peptide (CAMP), TLR-4, and HMGB-1 on inhibiting bacterial growth in Salmonella infection. This study is an experiment that uses a pre-post-test design. Mice balb/c were separated into three groups; group A received levofloxacin for five days, group B received a placebo, and group C was the control. Both groups, A and B, received an injection of S. Typhi strain thy1. Blood samples were taken from three groups on the 4th, 10th, and 30th day to calculate CAMP, TLR-4, and HMGB-1 mRNA gene expression levels. To determine bacterial colony, peritoneal fluid was taken three times on the 4th, 10th, and 30th day to calculate bacterial colony. This study aim to examine the interaction of Cathelicidin antimicrobial peptide (CAMP), TLR-4, and HMGB-1 on inhibiting bacterial growth in Salmonella infection. Our finding observed that the expression of mRNA CAMP was inversely related to bacte-rial colony count, which means that higher CAMP mRNA expression was associated with reduced bacterial colony count in groups A and B. The expression of HMGB-1 mRNA was found to be positively correlated with bacterial growth in group A. Meanwhile, TLR-4 mRNA expression did not significantly correlate with bacterial colony count in any groups. This study is an experiment that uses a pre-post-test design. Mice balb/c were separated into three groups; group A received levofloxacin for five days, group B received a placebo, and group C was the control. Both groups, A and B, received an injection of S. Typhi strain thy1. Blood samples were taken from three groups on the 4th, 10th, and 30th day to calculate CAMP, TLR-4, and HMGB-1 mRNA gene expression levels. To determine bacterial colony, peritoneal fluid was taken three times on the 4th, 10th, and 30th day to calculate bacterial colony. CAMP, TLR-4, and HMGB-1 affect bacterial infections. Higher expression CAMP mRNA levels lower colony counts. Meanwhile, decreasing TLR-4 and HMGB-1 mRNA expression were found during the study, due to reducing growth bacteria. The expression of mRNA CAMP and bacterial colony count correlated negatively. The expression of HMGB-1 mRNA correlated with bacterial growth. Higher CAMP mRNA expression was found to relate to reduced bacterial colony count in groups A and B using linear regression.
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探索卡特里西丁抗菌肽、Toll-Like 受体 4 和 HMGB-1 在细菌感染中的作用
伤寒沙门氏菌的脂多糖(LPS)会附着在 Toll-Like Receptor 4(TLR-4)上,引发炎症反应以对抗病原体。由于感染,免疫细胞会产生或从死亡细胞中被动分泌 HMGB1。此外,抗菌肽 cathelicidin 也被分泌出来,以中和并消除这些病原体。本研究旨在探讨猫科动物抗菌肽(CAMP)、TLR-4 和 HMGB-1 在沙门氏菌感染中抑制细菌生长的相互作用。小鼠 balb/c 被分为三组:A 组接受左氧氟沙星治疗五天,B 组接受安慰剂治疗,C 组为对照组。三组分别在第 4 天、第 10 天和第 30 天抽取血液样本,计算 CAMP、TLR-4 和 HMGB-1 mRNA 基因表达水平。本研究旨在探讨猫科动物抗菌肽(CAMP)、TLR-4 和 HMGB-1 在沙门氏菌感染中抑制细菌生长的相互作用。我们的研究结果表明,mRNA CAMP 的表达与细菌菌落数成反比,即 CAMP mRNA 表达越高,A 组和 B 组的细菌菌落数越少。小鼠 balb/c 被分为三组:A 组接受左氧氟沙星治疗五天,B 组接受安慰剂治疗,C 组为对照组。三组分别在第 4 天、第 10 天和第 30 天抽取血液样本,计算 CAMP、TLR-4 和 HMGB-1 mRNA 基因表达水平。为确定细菌菌落,在第 4 天、第 10 天和第 30 天分三次抽取腹腔液计算细菌菌落。CAMP、TLR-4 和 HMGB-1 对细菌感染有影响。CAMP mRNA 表达水平越高,菌落数越低。同时,在研究过程中发现,TLR-4 和 HMGB-1 mRNA 的表达量减少,这是因为细菌的生长速度降低了。HMGB-1 mRNA 的表达与细菌生长相关。使用线性回归法发现,CAMP mRNA 的高表达与 A 组和 B 组细菌菌落数的减少有关。
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来源期刊
Anti-Infective Agents
Anti-Infective Agents Pharmacology, Toxicology and Pharmaceutics-Pharmacology
CiteScore
1.50
自引率
0.00%
发文量
47
期刊介绍: Anti-Infective Agents publishes original research articles, full-length/mini reviews, drug clinical trial studies and guest edited issues on all the latest and outstanding developments on the medicinal chemistry, biology, pharmacology and use of anti-infective and anti-parasitic agents. The scope of the journal covers all pre-clinical and clinical research on antimicrobials, antibacterials, antiviral, antifungal, and antiparasitic agents. Anti-Infective Agents is an essential journal for all infectious disease researchers in industry, academia and the health services.
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