实验与检验医学
實驗與檢驗醫學
실험여검험의학
EXPERIMENTAL AND LABORATORY MEDICINE
2014年
6期
677-679,682
,共4页
魏丹丹%刘洋%邓琼%徐群飞%万腊根
魏丹丹%劉洋%鄧瓊%徐群飛%萬臘根
위단단%류양%산경%서군비%만석근
金黄色葡萄球菌%MRSA%耐药性%杀白细胞素
金黃色葡萄毬菌%MRSA%耐藥性%殺白細胞素
금황색포도구균%MRSA%내약성%살백세포소
Staphylococcus aureus%MRSA%Drug-resistance%PVL
目的:调查了解我院临床分离的124株金黄色葡萄球菌的耐药谱特征及PVL基因携带状况,为临床合理使用抗菌药物提供科学依据。方法采用Vitek2 Compact全自动微生物鉴定仪进行菌株鉴定及药物敏感试验,PCR法检测mecA基因、mecC基因和PVL基因。结果耐甲氧西林金黄色葡萄球菌(MRSA)的检出率为56.45%(70/124),MRSA主要分离自烧伤病区,其次是神经外科ICU。 MRSA菌株对青霉素G均耐药;对左氧氟沙星、庆大霉素、红霉素、四环素、复方新诺明和利福平的耐药率分别为57.1%、67.1%、85.7%、80.07%、28.6%、37.1%;MRSA对多种常用抗菌药物的耐药率普遍高于甲氧西林敏感金黄色葡萄球菌(MSSA),差异有统计学意义(P<0.05);MRSA和MSSA对呋喃妥因、喹奴普汀/达福普汀、利奈唑胺的耐药率分别为2.9%、11.4%、2.9%;0.0%、5.6%、5.6%,差异无统计学意义(P>0.05)。检出6株PVL阳性,其中MRSA和MSSA各占3株。结论我院分离的金黄色葡萄球菌对抗菌药物呈多重耐药性,MRSA菌株耐药率明显高于MSSA,应加强对MRSA的监测,指导临床合理使用抗菌药物,加强对呋喃妥因、喹奴普汀/达福普汀、利奈唑胺耐药菌株的检测及PVL基因的检测,防止此类菌株的播散。
目的:調查瞭解我院臨床分離的124株金黃色葡萄毬菌的耐藥譜特徵及PVL基因攜帶狀況,為臨床閤理使用抗菌藥物提供科學依據。方法採用Vitek2 Compact全自動微生物鑒定儀進行菌株鑒定及藥物敏感試驗,PCR法檢測mecA基因、mecC基因和PVL基因。結果耐甲氧西林金黃色葡萄毬菌(MRSA)的檢齣率為56.45%(70/124),MRSA主要分離自燒傷病區,其次是神經外科ICU。 MRSA菌株對青黴素G均耐藥;對左氧氟沙星、慶大黴素、紅黴素、四環素、複方新諾明和利福平的耐藥率分彆為57.1%、67.1%、85.7%、80.07%、28.6%、37.1%;MRSA對多種常用抗菌藥物的耐藥率普遍高于甲氧西林敏感金黃色葡萄毬菌(MSSA),差異有統計學意義(P<0.05);MRSA和MSSA對呋喃妥因、喹奴普汀/達福普汀、利奈唑胺的耐藥率分彆為2.9%、11.4%、2.9%;0.0%、5.6%、5.6%,差異無統計學意義(P>0.05)。檢齣6株PVL暘性,其中MRSA和MSSA各佔3株。結論我院分離的金黃色葡萄毬菌對抗菌藥物呈多重耐藥性,MRSA菌株耐藥率明顯高于MSSA,應加彊對MRSA的鑑測,指導臨床閤理使用抗菌藥物,加彊對呋喃妥因、喹奴普汀/達福普汀、利奈唑胺耐藥菌株的檢測及PVL基因的檢測,防止此類菌株的播散。
목적:조사료해아원림상분리적124주금황색포도구균적내약보특정급PVL기인휴대상황,위림상합리사용항균약물제공과학의거。방법채용Vitek2 Compact전자동미생물감정의진행균주감정급약물민감시험,PCR법검측mecA기인、mecC기인화PVL기인。결과내갑양서림금황색포도구균(MRSA)적검출솔위56.45%(70/124),MRSA주요분리자소상병구,기차시신경외과ICU。 MRSA균주대청매소G균내약;대좌양불사성、경대매소、홍매소、사배소、복방신낙명화리복평적내약솔분별위57.1%、67.1%、85.7%、80.07%、28.6%、37.1%;MRSA대다충상용항균약물적내약솔보편고우갑양서림민감금황색포도구균(MSSA),차이유통계학의의(P<0.05);MRSA화MSSA대부남타인、규노보정/체복보정、리내서알적내약솔분별위2.9%、11.4%、2.9%;0.0%、5.6%、5.6%,차이무통계학의의(P>0.05)。검출6주PVL양성,기중MRSA화MSSA각점3주。결론아원분리적금황색포도구균대항균약물정다중내약성,MRSA균주내약솔명현고우MSSA,응가강대MRSA적감측,지도림상합리사용항균약물,가강대부남타인、규노보정/체복보정、리내서알내약균주적검측급PVL기인적검측,방지차류균주적파산。
Objective To investigate the drug-resistance and carriage of Panton-Valentine leukocidin (PVL) gene of 124 Staphylococcus aureus isolated from the hospitalized patients to guide the clinical treatment. Methods 124 Staphylococcus aureus isolates were tested by Vitek 2 Compact automatic microorganism identifying, and the drug sensitivity tests were also performed by it. MecA gene、mecC gene and PVL gene were detected by PCR. Results Methicillin-resistant Staphylococcus aureus (MRSA) ac-counted for 56.45%(70/124), which mainly came from Burns ward and secondly came from Neurosurgery Intensive Care Unit (NICU). All MRSA strains were resistant to penicillin G, and the resistance rates of levofloxacin, gentamicin, erythromycin, tetracy-cline, SMZ-TMP and rifampicin were 57.1%, 67.1%, 85.7%, 80.07%, 28.6% and 37.1%, repectively. For many drug resistances, there was statistical difference between MRSA and methicillin susceptible Staphylococcus aureus (MSSA)(P<0.05). The drug resis-tance rates of MRSA were 2.9%, 11.4%, 2.9%in Nitrofurantoin, Quinupristin-Dalfoprisdn and Linezolid, 0.0%, 5.6%, 5.6%refer-ring to MSSA. 6 of 124 Staphylococcus aureus carried PVL genes. Conclusions The Staphylococcus aureus strains from our hos-pital were multi-drug resistant for antibiotics, and the drug resistance rate of the MRSA strains was higher than the MSSA strains. The surveillance of MRSA should be strengthened to guide clinical medicine, the same with the surveillance of Nitrofurantoin, Quinupristin-Dalfoprisdn and Linezolid resistant Staphylococcus aureus and PVL genes.