浙江医学
浙江醫學
절강의학
ZHEJIANG MEDICAL JOURNAL
2014年
22期
1856-1858
,共3页
赵仕勇%林先耀%王娟%吴亦栋%祁正红%邵启民%崔大伟
趙仕勇%林先耀%王娟%吳亦棟%祁正紅%邵啟民%崔大偉
조사용%림선요%왕연%오역동%기정홍%소계민%최대위
麻疹%粪便%病毒核酸%荧光定量%RT- PCR
痳疹%糞便%病毒覈痠%熒光定量%RT- PCR
마진%분편%병독핵산%형광정량%RT- PCR
Measles%Stool%Nucleic acid%Fluorescent quantitativn%RT- PCR
目的:探讨麻疹患儿肠道排毒情况和粪便病毒核酸快速检测的临床意义。方法38例临床诊断麻疹患儿,入院时均有发热、皮疹等麻疹感染症状。在入院2d内同时采集咽拭子和粪便标本。标本在冷链条件下送传染病诊治国家重点实验室,采用RT- PCR法检测麻疹病毒核酸及Ct值。同时对部分咽拭子和粪便标本扩增均阳性的PCR产物进行基因测序。结果38例患儿粪便麻疹病毒核酸阳性37例,占97.4%,Ct值23.8±3.04;咽拭子病毒核酸阳性35例,占92.1%,Ct值28.0±4.0。两者阳性率比较,差异无统计学意义(χ2=0.029,P>0.05);两组Ct值比较,差异有统计学意义(t=5.23,P<0.05)。3例患儿咽拭子和粪便标本的麻疹病毒基因型(均为H1a基因亚型)和核苷酸序列完全一致。结论粪便病毒核酸快速检测与咽拭子标本具有相同的临床诊断价值,粪便病毒核酸拷贝数高于咽拭子病毒核酸,且粪便标本的采集具有方便、无痛苦,依从性好,不易受人为因素的影响,值得推广。
目的:探討痳疹患兒腸道排毒情況和糞便病毒覈痠快速檢測的臨床意義。方法38例臨床診斷痳疹患兒,入院時均有髮熱、皮疹等痳疹感染癥狀。在入院2d內同時採集嚥拭子和糞便標本。標本在冷鏈條件下送傳染病診治國傢重點實驗室,採用RT- PCR法檢測痳疹病毒覈痠及Ct值。同時對部分嚥拭子和糞便標本擴增均暘性的PCR產物進行基因測序。結果38例患兒糞便痳疹病毒覈痠暘性37例,佔97.4%,Ct值23.8±3.04;嚥拭子病毒覈痠暘性35例,佔92.1%,Ct值28.0±4.0。兩者暘性率比較,差異無統計學意義(χ2=0.029,P>0.05);兩組Ct值比較,差異有統計學意義(t=5.23,P<0.05)。3例患兒嚥拭子和糞便標本的痳疹病毒基因型(均為H1a基因亞型)和覈苷痠序列完全一緻。結論糞便病毒覈痠快速檢測與嚥拭子標本具有相同的臨床診斷價值,糞便病毒覈痠拷貝數高于嚥拭子病毒覈痠,且糞便標本的採集具有方便、無痛苦,依從性好,不易受人為因素的影響,值得推廣。
목적:탐토마진환인장도배독정황화분편병독핵산쾌속검측적림상의의。방법38례림상진단마진환인,입원시균유발열、피진등마진감염증상。재입원2d내동시채집인식자화분편표본。표본재랭련조건하송전염병진치국가중점실험실,채용RT- PCR법검측마진병독핵산급Ct치。동시대부분인식자화분편표본확증균양성적PCR산물진행기인측서。결과38례환인분편마진병독핵산양성37례,점97.4%,Ct치23.8±3.04;인식자병독핵산양성35례,점92.1%,Ct치28.0±4.0。량자양성솔비교,차이무통계학의의(χ2=0.029,P>0.05);량조Ct치비교,차이유통계학의의(t=5.23,P<0.05)。3례환인인식자화분편표본적마진병독기인형(균위H1a기인아형)화핵감산서렬완전일치。결론분편병독핵산쾌속검측여인식자표본구유상동적림상진단개치,분편병독핵산고패수고우인식자병독핵산,차분편표본적채집구유방편、무통고,의종성호,불역수인위인소적영향,치득추엄。
Objective To evaluate the application of stool samples in detection of nucleic acid in children with measles. Methods Thirty eight children with a clinical diagnosis of measles were admitted in Hangzhou Children's Hospital from March to June 2013. The throat swabs and stool specimens were col ected within 2 days of admission. The specimens were examined with fluorescence quantitative RT- PCR for nucleic acid of measles virus. Results The viral nucleic acid was positive in 37 stool specimens (97.4%) with a Ct value of 23.8±3.04 and in 35 throat swabs samples (92.1%) with a Ct value of 28.0±4.0, respec-tively (positive rate:χ2=0.029, P>0.05;Ct value:t=5.23, P<0.05). The amplified PCR products were positive in gene sequencing. Conclusion The stool sample has the same diagnostic value as throat swab specimens in detection of measles viral nucleic acid and the former is more convenient with better compliance for col ection.