医学研究生学报
醫學研究生學報
의학연구생학보
JOURNAL OF MEDICAL POSTGRADUATE
2014年
7期
690-693
,共4页
刘青%施毅%朱素华%高卫卫%孙禾%苏欣
劉青%施毅%硃素華%高衛衛%孫禾%囌訢
류청%시의%주소화%고위위%손화%소흔
肺炎链球菌%生物膜%最低抑菌浓度%激光共聚焦扫描显微镜
肺炎鏈毬菌%生物膜%最低抑菌濃度%激光共聚焦掃描顯微鏡
폐염련구균%생물막%최저억균농도%격광공취초소묘현미경
Streptococcus pneumoniae%Biofilm%Minimal in-hibitory concentration%Confocal laser scanning microscope
目的:肺炎链球菌可形成生物膜。文中旨在研究青霉素不同最低抑菌浓度(minimal inhibitory concentration, MIC)的肺炎链球菌生物膜形成厚度的差别。方法收集2010年11月至2012年10月南京军区南京总医院、江苏省人民医院、江苏省中医院、南京医科大学第二附属医院、南京市鼓楼医院、东南大学附属中大医院、南京市第一医院等7家医院共147株肺炎链球菌,琼脂稀释法测定青霉素MIC,根据MIC分为≤0.065μg/mL组、0.5μg/mL组、2μg/mL组及≥4μg/mL组,每组选择4珠菌,共16珠菌;96孔板、24孔板培养生物膜24 h,分别在570 nm处测A值并且激光共聚焦扫描显微镜( confocal laser scanning micro-scope, CLSM)观察生物膜形成。结果生物膜半定量检测及CLSM显示所有菌株都形成生物膜。≤0.065μg/mL组平均A值(0.228±0.063)高于0.5μg/mL组(0.200±0.061)和≥4μg/mL组(0.186±0.050),差异均有统计学意义( P<0.05),但与2μg/mL组(0.203±0.049)差异无统计学意义(P>0.05);0.5μg/mL组、2μg/mL组≥4μg/mL组A值两两比较的差异无统计学意义(P>0.05)。结论青霉素MIC高的肺炎链球菌生物膜厚度有减弱的趋势,生物膜的形成是复杂的过程,受多种因素影响。
目的:肺炎鏈毬菌可形成生物膜。文中旨在研究青黴素不同最低抑菌濃度(minimal inhibitory concentration, MIC)的肺炎鏈毬菌生物膜形成厚度的差彆。方法收集2010年11月至2012年10月南京軍區南京總醫院、江囌省人民醫院、江囌省中醫院、南京醫科大學第二附屬醫院、南京市鼓樓醫院、東南大學附屬中大醫院、南京市第一醫院等7傢醫院共147株肺炎鏈毬菌,瓊脂稀釋法測定青黴素MIC,根據MIC分為≤0.065μg/mL組、0.5μg/mL組、2μg/mL組及≥4μg/mL組,每組選擇4珠菌,共16珠菌;96孔闆、24孔闆培養生物膜24 h,分彆在570 nm處測A值併且激光共聚焦掃描顯微鏡( confocal laser scanning micro-scope, CLSM)觀察生物膜形成。結果生物膜半定量檢測及CLSM顯示所有菌株都形成生物膜。≤0.065μg/mL組平均A值(0.228±0.063)高于0.5μg/mL組(0.200±0.061)和≥4μg/mL組(0.186±0.050),差異均有統計學意義( P<0.05),但與2μg/mL組(0.203±0.049)差異無統計學意義(P>0.05);0.5μg/mL組、2μg/mL組≥4μg/mL組A值兩兩比較的差異無統計學意義(P>0.05)。結論青黴素MIC高的肺炎鏈毬菌生物膜厚度有減弱的趨勢,生物膜的形成是複雜的過程,受多種因素影響。
목적:폐염련구균가형성생물막。문중지재연구청매소불동최저억균농도(minimal inhibitory concentration, MIC)적폐염련구균생물막형성후도적차별。방법수집2010년11월지2012년10월남경군구남경총의원、강소성인민의원、강소성중의원、남경의과대학제이부속의원、남경시고루의원、동남대학부속중대의원、남경시제일의원등7가의원공147주폐염련구균,경지희석법측정청매소MIC,근거MIC분위≤0.065μg/mL조、0.5μg/mL조、2μg/mL조급≥4μg/mL조,매조선택4주균,공16주균;96공판、24공판배양생물막24 h,분별재570 nm처측A치병차격광공취초소묘현미경( confocal laser scanning micro-scope, CLSM)관찰생물막형성。결과생물막반정량검측급CLSM현시소유균주도형성생물막。≤0.065μg/mL조평균A치(0.228±0.063)고우0.5μg/mL조(0.200±0.061)화≥4μg/mL조(0.186±0.050),차이균유통계학의의( P<0.05),단여2μg/mL조(0.203±0.049)차이무통계학의의(P>0.05);0.5μg/mL조、2μg/mL조≥4μg/mL조A치량량비교적차이무통계학의의(P>0.05)。결론청매소MIC고적폐염련구균생물막후도유감약적추세,생물막적형성시복잡적과정,수다충인소영향。
Objective Streptococcus pneumoniae can form biofilms .The aim of this study was to investigate the biofilm forma-tion of Streptococcus pneumoniae and the relationship with antibiotic resistance of penicillin etc . Methods A total of 147 clinical iso-lates of Streptococcus pneumoniae were collected from 7 teaching hospitals in Nanjing from 2010 to 2012.Minimal inhibitory concentration (MIC) of penicillin, erythromycin, cefuroxime and ceftriaxone were determined by agar dilution method .Streptococcus pneumoniae with various penicillin MIC was selected randomly as follow:MIC≤0.065μg/mL, 0.5μg/mL, 2μg/mL and≥4μg/mL, which was incuba-ted to form biofilms in 96-well plates and 24-well plates for 24 hours.The A values at 570 nm was measured and the biofilm was observed through confocal laser scanning microscope ( CLSM) . Results The biofilm semi-quantitative detection and CLSM both displayed that all strains formed biofilms.The A value of the group which penicillin MIC was ≤0.065μg/mL (0.228 ±0.063) was higher than the 0.5μg/mL group (0.200 ±0.061) and the≥4μg/mL group (0.186 ±0.050) (P<0.05) , and there was no difference among the groups which penicillin MIC were 0.5μg/mL, 2μg/mL and≥4μg/mL, respectively (P>0.05).The A value of the group which erythromycin MIC was ≤0.5μg/mL (0.211 ±0.068) was higher than the ≥4μg/mL group (0.201 ±0.052) (P>0.05).The A value of the group sensitive to cefuroxime (0.216 ±0.062) was higher than the group resistant to cefuroxime (0.196 ±0.054) (P<0.05). Conclusion Streptococcus pneumoniae can form biofilms .Streptococcus pneumoniae with high antibiotics MIC has a trend of weakened biofilm formation .