国际检验医学杂志
國際檢驗醫學雜誌
국제검험의학잡지
International Journal of Laboratory Medicine
2015年
17期
2461-2463
,共3页
冯福英%杨湘越%洪宇%郑宗富%张薇%蒋际城%曾琦
馮福英%楊湘越%洪宇%鄭宗富%張薇%蔣際城%曾琦
풍복영%양상월%홍우%정종부%장미%장제성%증기
奇异变形杆菌%耐药基因%整合子%脉冲场凝胶电泳
奇異變形桿菌%耐藥基因%整閤子%脈遲場凝膠電泳
기이변형간균%내약기인%정합자%맥충장응효전영
Proteus mirabilis%drug resistance gene%integron%pulsed-field gel electrophoresis
目的:了解该院神经内科病区奇异变形杆菌院内感染状况与耐药机制。方法对20株不重复奇异变形杆菌采用PCR法检测超广谱β内酰胺酶(ESBLs)、头孢菌素(AmpC)酶、碳青霉烯酶(KPC)和金属β内酰胺酶(MBLs)耐药基因并测序;PCR法检测整合子并测序;脉冲场凝胶电泳法分析菌株间亲缘关系;对这20株奇异变形杆菌进行药敏试验并分析。结果从这20株奇异变形杆菌中均检测出TEM‐1和CTX‐M‐14型耐药基因,10株菌中分离出CMY‐2型耐药基因。从19株菌中扩增出Ⅰ类整合子,分别整合的基因盒有“aacA4+cmlA1”,“dfrA12+orfF+ aadA2”和“dfrA32+ ereA+ aadA2”。脉冲场凝胶电泳结果聚类分析20株菌可分为P1~P11的11个PFGE型别,其中P1~P3的12株菌为同一克隆株。20株菌对美罗培南、阿米卡星、氨曲南、头孢他啶和哌拉西林/他唑巴坦的敏感率高。结论该院神经内科病区出现奇异变形杆菌同克隆株的传播;携带的耐药基因以CTX‐M‐14和CMY‐2型为主;Ⅰ类整合子携带率高,耐药基因盒以“aacA4+cmlA1”和“dfrA12+orfF+aadA2”为主;菌株对美罗培南、阿米卡星和氨曲南均为敏感;临床科室应同样重视由奇异变形杆菌引起的院内感染,加强感染控制措施。
目的:瞭解該院神經內科病區奇異變形桿菌院內感染狀況與耐藥機製。方法對20株不重複奇異變形桿菌採用PCR法檢測超廣譜β內酰胺酶(ESBLs)、頭孢菌素(AmpC)酶、碳青黴烯酶(KPC)和金屬β內酰胺酶(MBLs)耐藥基因併測序;PCR法檢測整閤子併測序;脈遲場凝膠電泳法分析菌株間親緣關繫;對這20株奇異變形桿菌進行藥敏試驗併分析。結果從這20株奇異變形桿菌中均檢測齣TEM‐1和CTX‐M‐14型耐藥基因,10株菌中分離齣CMY‐2型耐藥基因。從19株菌中擴增齣Ⅰ類整閤子,分彆整閤的基因盒有“aacA4+cmlA1”,“dfrA12+orfF+ aadA2”和“dfrA32+ ereA+ aadA2”。脈遲場凝膠電泳結果聚類分析20株菌可分為P1~P11的11箇PFGE型彆,其中P1~P3的12株菌為同一剋隆株。20株菌對美囉培南、阿米卡星、氨麯南、頭孢他啶和哌拉西林/他唑巴坦的敏感率高。結論該院神經內科病區齣現奇異變形桿菌同剋隆株的傳播;攜帶的耐藥基因以CTX‐M‐14和CMY‐2型為主;Ⅰ類整閤子攜帶率高,耐藥基因盒以“aacA4+cmlA1”和“dfrA12+orfF+aadA2”為主;菌株對美囉培南、阿米卡星和氨麯南均為敏感;臨床科室應同樣重視由奇異變形桿菌引起的院內感染,加彊感染控製措施。
목적:료해해원신경내과병구기이변형간균원내감염상황여내약궤제。방법대20주불중복기이변형간균채용PCR법검측초엄보β내선알매(ESBLs)、두포균소(AmpC)매、탄청매희매(KPC)화금속β내선알매(MBLs)내약기인병측서;PCR법검측정합자병측서;맥충장응효전영법분석균주간친연관계;대저20주기이변형간균진행약민시험병분석。결과종저20주기이변형간균중균검측출TEM‐1화CTX‐M‐14형내약기인,10주균중분리출CMY‐2형내약기인。종19주균중확증출Ⅰ류정합자,분별정합적기인합유“aacA4+cmlA1”,“dfrA12+orfF+ aadA2”화“dfrA32+ ereA+ aadA2”。맥충장응효전영결과취류분석20주균가분위P1~P11적11개PFGE형별,기중P1~P3적12주균위동일극륭주。20주균대미라배남、아미잡성、안곡남、두포타정화고랍서림/타서파탄적민감솔고。결론해원신경내과병구출현기이변형간균동극륭주적전파;휴대적내약기인이CTX‐M‐14화CMY‐2형위주;Ⅰ류정합자휴대솔고,내약기인합이“aacA4+cmlA1”화“dfrA12+orfF+aadA2”위주;균주대미라배남、아미잡성화안곡남균위민감;림상과실응동양중시유기이변형간균인기적원내감염,가강감염공제조시。
Objective To investigate the prevalence and resistance mechanisms of Proteus mirabilis in the ward of neurology de‐partment of our hospital .Methods For a total of 20 clinic isolates of Proteus mirabilis ,PCR were used for the detection of AmpC , ESBLs ,KPC and MBLs and then DNA sequencing was performed .The integrons were also detected by using PCR and then sequen‐cing was carried out .The genetic relationship between isolates were detected and analysed by pulsed‐field gel electrophoresis(PF‐GE) .The results of drug sensitivity tests were analysed .Results TEM‐1 and CTX‐M‐14 gene were found in all the 20 isolates ,the 10 isolates of Proteus mirabilis were also found carrying CMY‐2 gene .Class Ⅰ integrons were amplified from 19 strains carrying gene cassettes "aacA4+cmlA1","dfrA12+orfF+aadA2"and "dfrA32+ereA+aadA2" respectively .PFGE analysis revealed that the 20 isolates were grouped into 11 PFGE types P1-P11 ,the 12 isolates of P1-P3 were same clones .The sensitive rates of the i‐solates to Meropenem ,Amikacin ,Aztreonam ,Ceftazidime and Tazocin were high .Conclusion Nosocomial transmission of the same clone of Proteus mirabilis was appeared in the ward of neurology department of our hospital .The predominance drug‐resistance genes were CTX‐M‐14 andCMY‐2 .The incidence of carrying class Ⅰ integrons was high ,and the major gene cassettes were"aacA4+cmlA1"and "dfrA12+orfF+aadA2".The 20 isolates were all sensitive to Meropenem ,Amikacin and Aztreonam .Other Clinical departments should also pay attention to the nosocomial infection caused by Proteus mirabilis and strengthen the infection control measures .