寄生虫与医学昆虫学报
寄生蟲與醫學昆蟲學報
기생충여의학곤충학보
Acta Parasitology et Medica Entomologica Sinica
2015年
3期
141-146
,共6页
汪鹏程%熊小路%焦俊%龚文平%杨晓梅%温博海
汪鵬程%熊小路%焦俊%龔文平%楊曉梅%溫博海
왕붕정%웅소로%초준%공문평%양효매%온박해
恙虫病东方体%恙虫病%外膜蛋白%酶联免疫吸附试验
恙蟲病東方體%恙蟲病%外膜蛋白%酶聯免疫吸附試驗
양충병동방체%양충병%외막단백%매련면역흡부시험
Orientia tsutsugamushi%Tsutsugamushi disease%Outer membrane protein%Enzyme-linked immunosorbent assay
用恙虫病东方体的r47、 r56、 r58 kDa重组膜蛋白抗原包被建立酶联免疫吸附试验( ELISA ),对恙虫病东方体实验感染小鼠血清和临床患者血清做IgG抗体检测。8份恙虫病感染小鼠血清中除1份血清与r58 kDa蛋白的反应阴性外其他反应均为阳性;而这3个重组蛋白与贝氏柯克斯体( Q热病原体)、莫氏立克次体(地方性斑疹伤寒病原体)、黑龙江立克次体(远东斑点热病原体)感染小鼠血清反应均为阴性。另外,12份恙虫病患者血清对这3个蛋白的反应均有11份(92%)为阳性。另外, r47 kDa抗原对11份Q热患者血清、11份斑疹伤寒患者血清、13份斑点热患者血清的反应阳性率分别有27%、18%、23%,对r56 kDa抗原分别为27%、0%、8%,对r58 kDa抗原分别为18%、18%、23%。这些结果显示这3个重组蛋白抗原均有识别恙虫病东方体感染血清的良好特异性和敏感性,用这3种重组蛋白抗原建立的ELISA将为我国恙虫病血清学诊断提供新的实用方法。
用恙蟲病東方體的r47、 r56、 r58 kDa重組膜蛋白抗原包被建立酶聯免疫吸附試驗( ELISA ),對恙蟲病東方體實驗感染小鼠血清和臨床患者血清做IgG抗體檢測。8份恙蟲病感染小鼠血清中除1份血清與r58 kDa蛋白的反應陰性外其他反應均為暘性;而這3箇重組蛋白與貝氏柯剋斯體( Q熱病原體)、莫氏立剋次體(地方性斑疹傷寒病原體)、黑龍江立剋次體(遠東斑點熱病原體)感染小鼠血清反應均為陰性。另外,12份恙蟲病患者血清對這3箇蛋白的反應均有11份(92%)為暘性。另外, r47 kDa抗原對11份Q熱患者血清、11份斑疹傷寒患者血清、13份斑點熱患者血清的反應暘性率分彆有27%、18%、23%,對r56 kDa抗原分彆為27%、0%、8%,對r58 kDa抗原分彆為18%、18%、23%。這些結果顯示這3箇重組蛋白抗原均有識彆恙蟲病東方體感染血清的良好特異性和敏感性,用這3種重組蛋白抗原建立的ELISA將為我國恙蟲病血清學診斷提供新的實用方法。
용양충병동방체적r47、 r56、 r58 kDa중조막단백항원포피건립매련면역흡부시험( ELISA ),대양충병동방체실험감염소서혈청화림상환자혈청주IgG항체검측。8빈양충병감염소서혈청중제1빈혈청여r58 kDa단백적반응음성외기타반응균위양성;이저3개중조단백여패씨가극사체( Q열병원체)、막씨립극차체(지방성반진상한병원체)、흑룡강립극차체(원동반점열병원체)감염소서혈청반응균위음성。령외,12빈양충병환자혈청대저3개단백적반응균유11빈(92%)위양성。령외, r47 kDa항원대11빈Q열환자혈청、11빈반진상한환자혈청、13빈반점열환자혈청적반응양성솔분별유27%、18%、23%,대r56 kDa항원분별위27%、0%、8%,대r58 kDa항원분별위18%、18%、23%。저사결과현시저3개중조단백항원균유식별양충병동방체감염혈청적량호특이성화민감성,용저3충중조단백항원건립적ELISA장위아국양충병혈청학진단제공신적실용방법。
The enzyme-linked immunosorbent assay ( ELISA) with a recombinant outer membrane protein ( r47, r56, or r58 kDa) of Orientia tsutsugamushi was analyzed for specificity and sensitivity in detection of specific Ig G antibodies in sera from mice and patients suffered from O.tsutsugamushi infection.As a result, all of 8 serum specimens from mice experimentally infected with O.tsutsugamushi positively reacted with r47, 56 and r58 kDa protein respectively, except for that one serum negatively reacted with r58 kDa, while all of 8 sera from mice infected with Coxiella burnetii, Rickettsia mooseri or R.heilongjiangensis negatively reacted with the three proteins.In addition, 11 of 12 sera from patients with tsutsugamushi disease positively reacted with the three proteins, respectively, while 11 sera from patients with Q fever, 11 sera from patients with endemic typhus, and 13 sera from patients with spotted fever positively reacted to r47 kDa in the ratios of 28%, 18%, and 23%, to r56 kDa in the ratios of 28%, 0%, and 8%, and to r58 kDa in the ratios of 18%, 18%, and 23%, respectively.The results suggest that the ELISA coated with r47, r56, or r58 kDa has a good specificity and sensitivity for serological diagnosis of tsutsugamushi disease.