中华检验医学杂志
中華檢驗醫學雜誌
중화검험의학잡지
CHINESE JOURNAL OF LABORATORY MEDICINE
2010年
2期
126-131
,共6页
鲁辛辛%耿佳靖%李云川%周兵%袁梁%王向东%张孜%韩德民
魯辛辛%耿佳靖%李雲川%週兵%袁樑%王嚮東%張孜%韓德民
로신신%경가정%리운천%주병%원량%왕향동%장자%한덕민
鼻窦炎%真菌病%真菌%序列分析,RNA
鼻竇炎%真菌病%真菌%序列分析,RNA
비두염%진균병%진균%서렬분석,RNA
Sinusitis%Mycoses%Fungi%Sequence analysis,RNA
目的 建立ITS(包括ITSI-5.8 rRNA-ITS2)测序鉴定真菌性鼻窦炎病原的方法.方法 收集北京同仁医院2006-2008年,经临床与CT诊断为真菌性鼻窦炎,并行鼻内镜手术切除的组织标本270份.所有标本分别进行组织病理检查、压片直接镜检、真菌培养鉴定和核糖体RNA转录间隔区测序分析,通过方法比较,评价序列分析直接鉴定病原真菌的可行性,同时分析真菌性鼻窦炎病原学特征.结果 在270份标本中,组织病理阳性率为80.0%(216/270),压片阳性率为80.0%(216/270),真菌培养阳性率为53.0%(143/270),ITS测序阳性率为63.0%(170/270).经培养得到22个种,6个属.ITS测序鉴定32个种.培养与ITS序列种水平符合率为76.1%(102/143).结论 ITS测序可成为真菌鉴定的辅助工具.
目的 建立ITS(包括ITSI-5.8 rRNA-ITS2)測序鑒定真菌性鼻竇炎病原的方法.方法 收集北京同仁醫院2006-2008年,經臨床與CT診斷為真菌性鼻竇炎,併行鼻內鏡手術切除的組織標本270份.所有標本分彆進行組織病理檢查、壓片直接鏡檢、真菌培養鑒定和覈糖體RNA轉錄間隔區測序分析,通過方法比較,評價序列分析直接鑒定病原真菌的可行性,同時分析真菌性鼻竇炎病原學特徵.結果 在270份標本中,組織病理暘性率為80.0%(216/270),壓片暘性率為80.0%(216/270),真菌培養暘性率為53.0%(143/270),ITS測序暘性率為63.0%(170/270).經培養得到22箇種,6箇屬.ITS測序鑒定32箇種.培養與ITS序列種水平符閤率為76.1%(102/143).結論 ITS測序可成為真菌鑒定的輔助工具.
목적 건립ITS(포괄ITSI-5.8 rRNA-ITS2)측서감정진균성비두염병원적방법.방법 수집북경동인의원2006-2008년,경림상여CT진단위진균성비두염,병행비내경수술절제적조직표본270빈.소유표본분별진행조직병리검사、압편직접경검、진균배양감정화핵당체RNA전록간격구측서분석,통과방법비교,평개서렬분석직접감정병원진균적가행성,동시분석진균성비두염병원학특정.결과 재270빈표본중,조직병리양성솔위80.0%(216/270),압편양성솔위80.0%(216/270),진균배양양성솔위53.0%(143/270),ITS측서양성솔위63.0%(170/270).경배양득도22개충,6개속.ITS측서감정32개충.배양여ITS서렬충수평부합솔위76.1%(102/143).결론 ITS측서가성위진균감정적보조공구.
Objective To establish a molecular technique of internal transcribed spacer (ITS) sequencing to identify pathogenic fungi species from the fungal sinusitis tissues. Methods Total 270 sinusitis tissues samples were collected by endoscopic surgery from 2006 to 2008. The histopathology, organize spring clip culturation and ITS region (ITS region region of fungal rRNA, including ITS1-5. 8S rRNA-ITS2) sequencing were employed simultaneously. And then to evaluate the ITS sequencing as the tool for identification of pathogenic fungi directly from clinical samples. Results Of the 270 samples, histopathology positive rate was 80.0% (216/270) , organize spring clip positive rate was 80.0% (216/ 270), fungal culturation positive rate was 53.0% (143/270) , ITS region sequencing positive rate was 63. 0% [ (134 +28 +8)/270], There were 22 species and 6 genera identified by fungal culturation, and 32 species identified by ITS region sequencing. Conclusion ITS region sequencing will become a applicable tool in clinical laboratory in future.