羧甲基壳聚糖对口腔重要厌氧菌的抑菌性能评价

目的 :评价羧甲基壳聚糖对口腔重要厌氧菌的抑菌性能。方法 :选择与口腔疾病密切相关的厌氧菌 11株 ,采用梯度稀释法测定羧甲基壳聚糖的最低抑菌浓度 (MIC)。结果 :羧甲基壳聚糖对牙龈卟啉菌、放线共生放线菌、中间普氏菌、牙龈嗜二氧化碳纤维菌、黄褐嗜二氧化碳纤维菌、产黑色素普氏菌、白色念珠菌、牙髓卟啉菌、小齿普氏菌、变形链球菌、远缘链球菌、粘性放线菌的 MIC分别为 2 0 ,10 ,5,80 ,2 0 ,>80 ,2 0 ,5,2 0 ,10 ,60 ,40 mg/ml。结论 :羧甲基壳聚糖对多数与口腔疾病密切相关的厌氧菌有一定抑制作用 ,而对产黑色素普氏菌的抑菌性不明显     

类芽孢杆菌BD3526抑菌活性物质的初步分离及性质测定北大核心CSCD

本实验以一株类芽孢杆菌BD3526为研究对象,采用丙酮浸提菌体得到抑菌活性粗品,通过Sephadex LH-20对样品进行初步纯化,结果表明粗品对藤黄微球菌CGMCC1.1848的最低抑菌浓度(MIC)为12.5 mg/m L,对金黄色葡萄球菌CGMCC1.879和单增李斯特菌CGMCC1.9136的MIC为25 mg/m L;Sephadex LH-20纯化样品对藤黄微球CGMCC1.1848的MIC为1 mg/m L,对金黄色葡萄球菌CGMCC1.879和单增李斯特菌CGMCC1.9136的MIC为2 mg/m L。样品经链霉蛋白酶处理后,活性基本消失。经加热、酸碱、胰蛋白酶、胃蛋白酶、脂肪酶、蛋白酶K处理后,活性没有明显变化。因此,类芽孢杆菌BD3526产生的是一种细菌素类的抑菌物质,该抑菌物质在食品和医疗行业有广阔的应用前景。     

大肠杆菌外膜蛋白ompW基因敲除菌的构建及其对两种抗生素的敏感性

探讨大肠杆菌ompW基因敲除后,硫酸新霉素和氨苄青霉素对敲除菌最低抑菌浓度(MIC)和生存率的影响,进而分析OmpW的功能.[方法]运用Red重组技术将大肠杆菌K12染色体上基因ompW敲除,构建缺陷株△ompW.然后分别测定硫酸新霉素和氨苄青霉素对正常菌和△ompW菌的最小抑菌浓度(MIC)及次抑菌浓度(1/2 MIC)下K12和△ompW菌的生存率.[结果]经PCR鉴定和通过提取膜蛋白进行western blot 分析表明,成功获得ompW敲除菌.抗生素分析表明,K12菌对硫酸新霉素的MIC为8.0 μg/mL,生存率为98.0％;△ompW菌对新霉素的MIC为1.7 μg/mL,而其生存率仅为39.0％.而k12对氨苄新霉素的MIC为16.0 μg/mL,△ompW为3.3 μg/mL;1/2 MIC下K12生存率为70.4％,而△ompW为30.3％.[结论]ompW基因缺陷株对两抗生素的敏感性大大增强,表明ompW在细菌抗性方面起着关键作用.     

骏枣内生生防细菌的分离、筛选与鉴定

选择交城骏枣(Zizyphus jujube cv.Jiaocheng Junzao)作为分离内生细菌的材料,从中共分离到18株内生菌株,运用平板对峙法从中筛选出5株对大枣病原菌及部分植物病原菌有拮抗作用的内生细菌。抑菌试验结果表明:筛选出的5株细菌对刺盘胞菌Colletotrichum gloeosporides、链格孢菌Alternaria alternata、尖孢镰刀菌Fusarium oxysporium、烟草赤星病菌Alternarial longipes、稻瘟病菌Pyricularia oryzae、人参立枯病菌Rhizoctonia solani、人参菌核病菌Sclerotinia schinseng和小麦根腐病菌Bipolaris sorokiniana均有一定的抑菌活性。对这5株内生细菌进行了形态特征观察和生理生化鉴定。     

247例颌面部感染的细菌学研究

采用需氧和厌氧培养方法,分离培养２４７例颌面部感染标本的细菌。结果表明口腔颌面部感染以牙源性颌面部感染最多见,其感染率为８７９％。颌面部感染的细菌学特点是：①厌氧菌感染为主,其感染率在牙源性感染为９６％,非牙源性感染为７３７％,可培养的优势厌氧菌是普氏菌、叶啉单胞菌、梭杆菌、消化链球菌,其次是放线菌、优杆菌和二氧化碳噬纤维菌、口腔链球菌群细菌是主要的兼性厌氧菌,其次是嗜血菌。②由定植于口腔的细菌引发的内源性感染。③复数菌和混合菌感染为主     

竹荪提取物对食源性细菌的抑菌特性研究

利用4种方法获得棘托竹荪和长裙竹荪的提取物,以5种食源性致病细菌单增李斯特菌、金黄色葡萄球菌、肠炎沙门菌、大肠埃希菌O157H7、副溶血性弧菌为供试菌,比较其MIC(最低抑菌浓度)和MBC(最低杀菌浓度)。超声波辅助破碎竹荪干粉,制取水、乙醇和石油醚为提取介质的浸提物以及竹荪挥发油,利用液体培养基连续稀释法对5种供试菌进行抑菌实验。所有提取物对供试菌都具有抑菌活性;长裙竹荪提取物的综合抑菌能力高于棘托竹荪提取物;水提物和挥发油的抑菌效果最好;2种竹荪提取物对革兰阴性菌和革兰阳性菌的抑菌作用存在互补效应。竹荪提取物对5种食源性细菌的生长有较好的抑制作用,可应用2种竹荪的提取物复配,开发天然食品防腐剂。     

两种中药剂型的体外抑菌作用观察

目的比较黄连等20种中药水煎剂与免煎颗粒剂对56株临床分离的金黄色葡萄球菌的体外抑菌效果。方法采用M-H琼脂稀释法检测20种中药水煎剂与免煎颗粒剂对MSSA(甲氧西林敏感金黄色葡萄球菌)、MRSA(耐甲氧西林金黄色葡萄球菌)的体外抑菌作用,测定MIC50(药物抑制50%细菌时的最小浓度)、MIC90(药物抑制90%细菌时的最小浓度),MIC(最小抑菌浓度),并作比较。结果 20种中药的水煎剂和免煎颗粒对56株受试菌显示了不同程度的抑菌作用,以五倍子抑菌效果最好,水煎剂抑菌效果比相应的免煎颗粒好。结论两种中药剂型在抗感染中,均具有临床实际应用价值,而水煎剂抑菌效果稍强于相应的免煎颗粒剂型。     

千里光抗菌作用的数量性状分析

应用倍比稀释法检测18份千里光（Senecio scandens Buch-Ham）水煎剂对7种细菌的抗菌效果。最低抑菌浓度（minimal inhibitory concentration,MIC）检测结果表明,千里光对金黄色葡萄球菌的抗菌作用最强,对铜绿假单胞菌的抗菌效果最差。比较不同细菌的MIC值发现,温和气单胞菌共检测出4个不同的MIC值,金黄色葡萄球菌、铜绿假单胞菌、大肠埃希菌、甲型副伤寒杆菌、福氏痢疾杆菌和迟钝爱德华菌的MIC值为5个,迟钝爱德华菌的MIC值最多,表现出6个MIC梯度值。本研究结果提示千里光个体有效抗菌组分的多样性,也意味着千里光抗菌药理学性状为多基因控制的数量性状。     

水产动物常见病原菌的耐药性分析及中草药体外抑菌活性的检测

目的了解安徽省水产动物常见病原菌的耐药现状和耐药机制,探讨27种单味中草药和5个中草药复方配伍对耐药菌株的体外抑菌活性。方法分别采用K-B纸片琼脂扩散法和双纸片增效法检测常见病原菌的耐药性和ESBLs,同时使用平板打孔法和改良微量稀释法检测中草药的体外抑菌活性。结果4种常见病原菌的23个分离株对常用的5类抗生素均呈现不同程度的耐药性,其中铜绿假单胞菌的耐药谱最广,对14种抗生素的耐药率均为100%。供试菌中仅检出2株铜绿假单胞菌为产ESBLs株,检出率为8.69%。黄连、大黄、金银花、夏枯草、地锦草、丹皮、马齿苋和连翘8种中草药对供试耐药株均有较强的抑制活性,其中黄连、大黄和金银花的抑菌活性尤为明显,其MIC值分别介于1.96~125 g/L、7.84~125 g/L和15.68~250 g/L。5个复方配伍中以复方5的配伍效果最好,其MIC值为1.96~15.68 g/L,抑菌活性显著优于单味药;其次是复方1和复方3,其MIC值为1.96~62.72 g/L;复方2和复方4的配伍效果差,其MIC值为31.36~125 g/L。结论4种23株常见病原菌均为耐药菌株,产生ESBLs是铜绿假单胞菌高度多重耐药的主要机制之一。黄连、大黄、金银花和复方5配伍对常见病原菌耐药株具有良好的抑菌活性。     

抗菌脂肽制备羧甲基壳聚糖纳米粒稳定混悬液及其抑菌活性

利用抗菌脂肽解决羧甲基壳聚糖纳米粒制备过程中出现的团聚问题,并考察其对羧甲基壳聚糖纳米粒的抑菌效果影响.通过抗菌脂肽乳化分散离子交联法制备羧甲基壳聚糖纳米粒,静置观察其稳定性,乌氏粘度计测定其粘度变化,扫描电镜考察其形态改变,比浊法测定不同浓度纳米粒溶液对金黄色葡萄球菌和大肠埃希菌的抑制作用.实验发现,加入抗菌脂肽制备的纳米粒稳定性好,粘度降低,形态均一,并能显著增强对金黄色葡萄球菌和大肠埃希菌的抑制作用.结果表明,抗菌脂肽的加入能很好的解决纳米粒制备过程中出现的团聚现象,而且其抑菌效果也有很大改善.     

Antibacterial activity of ethanolic and aqueous extracts of Acacia aroma Gill. ex Hook et Arn

The purpose of the present study was to investigate the antibacterial activity of seven ethanolic extracts and three aqueous extracts from various parts (leaves, stems and flowers) of A. aroma against 163 strains of antibiotic multi-resistant bacteria. The disc diffusion assay was performed to evaluate antibacterial activity of the A. aroma crude extracts, against several Gram-positive bacteria (E. faecalis, S. aureus, coagulase-negative stahylococci, S. pyogenes, S. agalactiae, S. aureus ATCC 29213, E. faecalis ATCC 29212) and Gram-negative bacteria (E. coli., K. pneumoniae, P. mirabilis, E. cloacae, S. marcescens, M morganii, A. baumannii, P. aeruginosa, S. maltophilia, E. coli ATCC 35218, P. aeruginosa ATCC 27853, E. coli ATCC 25922). All ethanolic extracts showed activity against gram-positive bacteria. Among all obtained extracts, only leaf and flower fluid extracts showed activity against Gram-negative bacteria. Based on this bioassay, leaf fluid extracts tended to be the most potent, followed by flower fluid extracts. Minimal inhibitory concentration (MIC) values of extracts and antibiotics were comparatively determined by agar and broth dilution methods. Both extracts were active against S. aureus, coagulase-negative stahylococci, E. faecalis and E. faecium and all tested Gram-negative bacteria with MIC values from 0.067 to 0.308 mg/ml. In this study the minimal bactericidal concentration (MBC) values were identical or twice as high than the corresponding MIC for leaf extracts and four or eight times higher than MIC values for flower extracts. This may indicate a bactericidal effect. Stored extracts have similar antibacterial activity as recently obtained extracts. The A. aroma extracts of leaves and flowers may be useful as antibacterial agents against Gram- negative and Gram-positive antibiotic multi-resistant microorganisms.     

Antimicrobial effect of Korean propolis against the mutans streptococci isolated from Korean

The aim of this study was to determine the optimal concentration of Korean propolis against clinical isolates of mutans streptococci (MS) from Koreans. The antimicrobial activity was evaluated using the minimum inhibitory concentration (MIC) and time-kill curves against mutans streptococci. The MIC(90) values of propolis for MS were 35 μg/ml. Propolis had a bacteriostatic effect on Streptococcus mutans ATCC 25175(T) and bactericidal effects on Streptococcus sobrinus ATCC 33478(T) at > 2 × MIC (70 μg/ml). These results suggest that the propolis can be used in the development of oral hygiene products for the prevention of dental caries.     

A newly isolated Streptomyces sp. CS392 producing three antimicrobial compounds

With the aim of isolating new microbes capable of producing strong antimicrobial substances, strain CS392 was screened from 700 soil isolates preserved in our laboratory. The strain was related to genus Streptomyces based on various characteristics. Three highly active antimicrobial compounds, C1, C2 and C3, produced by the strain were purified by solvent extraction followed by silica gel column chromatography. These compounds were highly active against various Gram-positive resistant bacteria such as methicillin-resistant Staphylococcus aureus (MRSA), vancomycin-resistant Staphylococcus aureus (VRSA), and vancomycin-resistant Enterococcus (VRE). Among three, C3 was the most active against MRSA and VRSA with minimal inhibitory concentration (MIC) of 2 μg/ml while C2 and C3 had MIC values of 4 μg/ml for the strains. In case of Bacillus subtilis ATCC6633, C1 and C3 were more effective with MIC values of 0.5 μg/ml than C2 with MIC of 2 μg/ml. Those antibiotics were variably active (MIC of 4-32 μg/ml) against Micrococcus luteus ATCC 9341, Enterococcus faecalis ATCC 29212, Mycobacterium smegmatis ATCC 9341 and VRE.     

Synthesis, characterization and antimicrobial activity of new aliphatic sulfonamide

A series of novel aliphatic sulfonamide derivatives (1-7) were synthesized and characterized by elemental analyses, FT-IR, (1)H NMR, (13)C NMR and LC-MS techniques. All the synthesized compounds were evaluated in vitro as antimicrobial agents against representative strains of Gram-positive (Staphylococcus aureus ATCC 25953, Bacillus cereus ATCC 6633 and Listeria monocytogenes ATCC Li6 (isolate), Gram-negative bacteria (Escherichia coli ATCC 11230) and antifungal agent against Candida albicans (clinical isolate) by both disc diffusion and minimal inhibition concentration (MIC) methods. All these bacteria and fungus studied were screened against some antibiotics to compare with our chemicals' zone diameters. Our aliphatic sulfonamides have highest powerful antibacterial activity for Gram-negative bacteria than Gram-positive bacteria and antibacterial activity decreases as the length of the carbon chain increases.     

Antibacterial abietane-type diterpenoid, taxodone from Metasequoia glyptostroboides Miki ex Hu

In an attempt to isolate bioactive constituents, ethyl acetate cone extract of Metasequoia glyptostroboides was subjected to a column chromatographic analysis that resulted in isolation of an abietane-type diterpenoid, taxodone. Its structure was elucidated by spectroscopic means. Further, taxodone showed potential antibacterial effect as diameters of zones of inhibition against foodborne pathogenic bacteria, such as Listeria monocytogenes ATCC 19166, Salmonella typhimurium KCTC 2515, S. enteritidis KCTC 2021, Escherichia coli ATCC 8739, E. coli O157:H7 ATCC 43888, Enterobacter aerogenes KCTC 2190, Staphylococcus aureus ATCC 6538 and S. aureus KCTC 1916, were found in the range of 9.4 to 14.2 mm. The minimum inhibitory concentration (MIC) and minimum bactericidal concentration (MBC) values of taxodone against the employed bacterial pathogens were found in the range of 250 to 1000 and 250 to less than 2000 microg/ml, respectively. Also the compound had a strong antibacterial effect on the viable counts of the tested bacteria. These findings indicate that the bioactive compound taxodone present in M. glyptostroboides could be used as an antibacterial agent in food industry to inhibit the growth of certain important foodborne pathogens.     

Lipophilic gold(I) complexes with 1,3,4-oxadiazol-2-thione or 1,3-thiazolidine-2-thione moieties: synthesis and their cytotoxic and antimicrobial activities

Novel lipophilic gold(I) complexes containing 1,3,4-oxadiazol-2-thione or 1,3-thiazolidine-2-thione derivatives were synthesized and characterized by IR, high resolution mass spectrometry, and ¹H, ¹³C ³¹P NMR. The cytotoxicity of the compounds was evaluated considering cisplatin and/or auranofin as reference in different tumor cell lines: colon cancer (CT26WT), metastatic skin melanoma (B16F10), breast adenocarcinoma (MCF-7), cervical carcinoma (HeLa), glioblastoma (M059 J). Normal human lung fibroblasts (GM07492-A) and kidney normal cell (BHK-21) were also evaluated. The gold(I) complexes were more active than their respective free ligands and cisplatin. Furthermore, antibacterial activity was evaluated against Gram-positive bacteria Staphylococcus aureus ATCC 25213, Staphylococcus epidermidis ATCC 12228 and Gram-negative bacteria Escherichia coli ATCC 11229 and Pseudomonas aeruginosa ATCC 27853 and expressed as the minimum inhibitory concentration (MIC). The complexes exhibited lower MIC values when compared to the ligands and chloramphenicol against Gram-positive bacteria and Gram-negative bacteria. Escherichia coli was sensitive one to the action of gold(I) complexes.     

抗多重耐药病原菌的越南槐内生菌TRPH-35的抗菌活性及其鉴定

以大肠杆ATCC25922、金黄色葡萄球菌ATCC25923及其临床多重耐药分离株ETEC-AD9、MRSA-DF12共4株人体病原细菌为靶标菌,采用琼脂块法从越南槐内生真菌中筛选抗菌活性菌株,并以改良的微量肉汤稀释法测定其代谢产物的最小抑菌浓度;根据形态和分子特征鉴定拮抗菌株的分类学地位。结果表明,菌株TRPH-35的活菌块对各病原细菌的抑菌圈直径与阳性对照相当;其代谢产物对各病原菌的最小抑菌浓度为20~40μg/mL;初步鉴定该菌株为刺盘孢。本研究结果表明,菌株TRPH-35鉴定为刺盘孢,对参试病原细菌均显示强的抗菌活性,具有较大的开发应用潜力。     

Synergistic effects between silibinin and antibiotics on methicillin-resistant Staphylococcus aureus isolated from clinical specimens

Methicillin-resistant Staphylococcus aureus (MRSA) is a dangerous microorganism, and creates serious medical problems. It causes many types of infections in humans and often acquires multi-drug resistance. In this study, silibinin was evaluated against 20 clinical isolates of MRSA, either alone or in combination with ampicillin or oxacillin, using a checkerboard assay. The silibinin exhibited good activity against isolates of MRSA, and MRSA ATCC33952 and MSSA ATCC25923, with minimum inhibitory concentrations/minimum bactericidal concentrations (MICs/MBCs) ranging between 2-8/4-16 μg/mL, for ampicillin 2-1024/2-2048 μg/mL, and for oxacillin 0.25-32/0.5-64 μg/mL. The range of MIC(50) and MIC(90) were 0.5-4 μg/mL and 2-8 μg/mL, respectively. The MICs/MBCs for the combination of silibinin plus oxacillin or ampicillin were reduced by ≥4-fold against the MRSA isolates tested, demonstrating a synergistic effect, as defined by a fractional inhibitory concentration index (FICI) of ≤0.5. Furthermore, a time-kill study evaluating the growth of the tested bacteria showed that growth was completely attenuated after 2-5 h of treatment with the 1/2 MIC of silibinin, regardless of whether it was administered alone or with oxacillin (1/2 MIC) or ampicillin (1/2 MIC). In conclusion, silibinin exerted synergistic effects when administered with oxacillin or ampicillin and the antibacterial activity and resistant regulation of silibinin against clinical isolates of MRSA might be useful in controlling MRSA infections.     

Antibacterial activity of coumarins

The antibacterial activity of coumarin per se and other 45 coumarin derivatives was tested against strains of Bacillus cereus MIP 96016, Escherichia coli ATCC 25922, Pseudomonas aeruginosa ATCC 27853, and Staphylococcus aureus ATCC 25923. The inhibitory effects of coumarins were affected by their substitution patterns. Osthenol (44) showed the most effective antibacterial activity against Gram-positive bacteria with MIC values ranging between 125 and 62.5 microg/ml. These results suggested that the prenyl chain of 44 at position 8 and the presence of OH at position 7 of the benzenic ring are required for the antibacterial activity against these strains.