中国医师杂志
中國醫師雜誌
중국의사잡지
JOURNAL OF CHINESE PHYSICIAN
2011年
3期
324-327
,共4页
石玉玲%徐少珊%孙朝晖%陈丽丹%唐玲玲
石玉玲%徐少珊%孫朝暉%陳麗丹%唐玲玲
석옥령%서소산%손조휘%진려단%당령령
梭菌,产气荚膜/分离和提纯%聚合酶链反应/方法%气性坏疽/诊断
梭菌,產氣莢膜/分離和提純%聚閤酶鏈反應/方法%氣性壞疽/診斷
사균,산기협막/분리화제순%취합매련반응/방법%기성배저/진단
Clostridium perfringens/IP%Polymerase chain reaction/MT%Gas gangrene/DI
目的 利用产气荚膜梭菌qPCR法检测A型产气荚膜梭菌(Clostridium perfringens type A)感染小鼠的后肢的气性坏疽动物模型和一例阳性病例,以验证此法在早期诊断优势.方法 小鼠随机分成4组,10只/组分别肌肉注射3.5×109、3.5×108和3.5×107cfu/ml浓度的A型产气荚膜梭菌(ATCC13124)菌液0.1 ml,空白对照组肌肉注射生理盐水0.1 ml,建立小鼠感染的动物模型,利用产气荚膜梭菌qPCR方法 对动物模型及一例病例进行检测分析.结果 不同浓度菌液组(3.5×109、3.5×108、3.5×107cfu/ml实验组)和对照组在肌肉注射72 h内的死亡率为:90%、70%、10%和0;各组平均存活时间(hh:mm)依次为:20∶43±11∶12、37∶24±25∶39、68∶36±10∶45和72∶00±0∶00,各组荧光定量Ct值均值为:21.21±2.69、28.45±2.74、32.49±2.87和0.00±0.00,组间比较差异均有统计学意义(P<0.05).利用该法检测病者两处分泌物,Ct值为30.67、30.44.结论 利用产气荚膜梭菌qPCR法成功检测出未发病的小鼠中的产气荚膜梭菌,并成功的应用于一例病例中.
目的 利用產氣莢膜梭菌qPCR法檢測A型產氣莢膜梭菌(Clostridium perfringens type A)感染小鼠的後肢的氣性壞疽動物模型和一例暘性病例,以驗證此法在早期診斷優勢.方法 小鼠隨機分成4組,10隻/組分彆肌肉註射3.5×109、3.5×108和3.5×107cfu/ml濃度的A型產氣莢膜梭菌(ATCC13124)菌液0.1 ml,空白對照組肌肉註射生理鹽水0.1 ml,建立小鼠感染的動物模型,利用產氣莢膜梭菌qPCR方法 對動物模型及一例病例進行檢測分析.結果 不同濃度菌液組(3.5×109、3.5×108、3.5×107cfu/ml實驗組)和對照組在肌肉註射72 h內的死亡率為:90%、70%、10%和0;各組平均存活時間(hh:mm)依次為:20∶43±11∶12、37∶24±25∶39、68∶36±10∶45和72∶00±0∶00,各組熒光定量Ct值均值為:21.21±2.69、28.45±2.74、32.49±2.87和0.00±0.00,組間比較差異均有統計學意義(P<0.05).利用該法檢測病者兩處分泌物,Ct值為30.67、30.44.結論 利用產氣莢膜梭菌qPCR法成功檢測齣未髮病的小鼠中的產氣莢膜梭菌,併成功的應用于一例病例中.
목적 이용산기협막사균qPCR법검측A형산기협막사균(Clostridium perfringens type A)감염소서적후지적기성배저동물모형화일례양성병례,이험증차법재조기진단우세.방법 소서수궤분성4조,10지/조분별기육주사3.5×109、3.5×108화3.5×107cfu/ml농도적A형산기협막사균(ATCC13124)균액0.1 ml,공백대조조기육주사생리염수0.1 ml,건립소서감염적동물모형,이용산기협막사균qPCR방법 대동물모형급일례병례진행검측분석.결과 불동농도균액조(3.5×109、3.5×108、3.5×107cfu/ml실험조)화대조조재기육주사72 h내적사망솔위:90%、70%、10%화0;각조평균존활시간(hh:mm)의차위:20∶43±11∶12、37∶24±25∶39、68∶36±10∶45화72∶00±0∶00,각조형광정량Ct치균치위:21.21±2.69、28.45±2.74、32.49±2.87화0.00±0.00,조간비교차이균유통계학의의(P<0.05).이용해법검측병자량처분비물,Ct치위30.67、30.44.결론 이용산기협막사균qPCR법성공검측출미발병적소서중적산기협막사균,병성공적응용우일례병례중.
Objective To detect of clostridium perfringens by qPCR in mouse models and a clinical case in order to offer early diagnosis.Methods 40 Kunming mice were randomly grouped and intramuscular injected clostridium perfringens type A in leg 0.1 ml(3.5 × 109cfu/ml or 3.5 × 108cfu/ml or 3.5× 107cfu/ml,diluted with saline),while control group was injected with 9% sodium chloride 0.1ml.The mouse models and a clinical case were detected by qPCR.Results The death rate of 3.5 × 109,3.5 × 108,3.5 × 107cfu/ml and the blank group were 90%,70%,10% and 0% after intramuscular injection for 72 h spectively.The mean Ct values among these groups were 21.21 ±2.69,28.45 ±2.74,32.49 ±2.87 and 0.00 ± 0.00(P < 0.05).The Ct values of the patient were 30.67 and 30.44.Conclusions Cclostridium perfringens could be successful identified with qPCR in mouse models when the mice still did not show any symptoms.