{"title":"石蜡包埋组织切片中曲霉和新生霉菌分子鉴定方法的发展。","authors":"P J Paterson, S Seaton, J McLaughlin, C C Kibbler","doi":"10.1136/mp.56.6.368","DOIUrl":null,"url":null,"abstract":"<p><strong>Background/aims: </strong>Invasive infection with emerging moulds is increasing in incidence and reliable methods for speciating these organisms in tissue sections need to be developed.</p><p><strong>Methods: </strong>Two methods for extracting fungal DNA from paraffin wax embedded tissue sections, based on the TaKaRa DEXPAT kit and QIAamp DNA mini kit, were optimised and compared. DNA was amplified by PCR using pan-fungal probes, and detected by Southern blot hybridisation using a high stringency method with a probe specific for Aspergillus fumigatus and A flavus.</p><p><strong>Results: </strong>The method based on the TaKaRa DEXPAT kit, with additional steps using lyticase and ethanol precipitation, was superior. Less than 10 conidia were detectable using spiked samples and a positive result was obtained with 100% of clinical samples known to be culture positive for A fumigatus. Other moulds could be identified by using species specific probes or by sequencing PCR products.</p><p><strong>Conclusions: </strong>The method based on the TaKaRa DEXPAT kit could detect less than 10 conidia/sample. The method allowed accurate identification of A fumigatus and A flavus and other species could be identified using species specific probes or by DNA sequencing. These methods will provide a valuable diagnostic tool for both patient management and future antifungal and epidemiological studies.</p>","PeriodicalId":79512,"journal":{"name":"Molecular pathology : MP","volume":"56 6","pages":"368-70"},"PeriodicalIF":0.0000,"publicationDate":"2003-12-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1136/mp.56.6.368","citationCount":"36","resultStr":"{\"title\":\"Development of molecular methods for the identification of aspergillus and emerging moulds in paraffin wax embedded tissue sections.\",\"authors\":\"P J Paterson, S Seaton, J McLaughlin, C C Kibbler\",\"doi\":\"10.1136/mp.56.6.368\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><strong>Background/aims: </strong>Invasive infection with emerging moulds is increasing in incidence and reliable methods for speciating these organisms in tissue sections need to be developed.</p><p><strong>Methods: </strong>Two methods for extracting fungal DNA from paraffin wax embedded tissue sections, based on the TaKaRa DEXPAT kit and QIAamp DNA mini kit, were optimised and compared. DNA was amplified by PCR using pan-fungal probes, and detected by Southern blot hybridisation using a high stringency method with a probe specific for Aspergillus fumigatus and A flavus.</p><p><strong>Results: </strong>The method based on the TaKaRa DEXPAT kit, with additional steps using lyticase and ethanol precipitation, was superior. Less than 10 conidia were detectable using spiked samples and a positive result was obtained with 100% of clinical samples known to be culture positive for A fumigatus. Other moulds could be identified by using species specific probes or by sequencing PCR products.</p><p><strong>Conclusions: </strong>The method based on the TaKaRa DEXPAT kit could detect less than 10 conidia/sample. The method allowed accurate identification of A fumigatus and A flavus and other species could be identified using species specific probes or by DNA sequencing. These methods will provide a valuable diagnostic tool for both patient management and future antifungal and epidemiological studies.</p>\",\"PeriodicalId\":79512,\"journal\":{\"name\":\"Molecular pathology : MP\",\"volume\":\"56 6\",\"pages\":\"368-70\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2003-12-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://sci-hub-pdf.com/10.1136/mp.56.6.368\",\"citationCount\":\"36\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Molecular pathology : MP\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.1136/mp.56.6.368\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Molecular pathology : MP","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1136/mp.56.6.368","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 36
摘要
背景/目的:新兴霉菌的侵袭性感染发病率正在增加,需要开发可靠的方法在组织切片中确定这些生物体的物种。方法:以TaKaRa DEXPAT试剂盒和QIAamp DNA mini试剂盒为基础,优化比较两种提取石蜡包埋组织切片真菌DNA的方法。采用泛真菌探针扩增DNA,并采用烟曲霉和黄曲霉特异性探针高强度杂交法进行Southern blot检测。结果:以TaKaRa DEXPAT试剂盒为基础,添加裂解酶和乙醇沉淀的方法具有优越性。使用加标样品可检测到不到10个分生孢子,并且100%的临床样本已知为烟曲霉培养阳性,结果为阳性。其他霉菌可以通过使用物种特异性探针或测序PCR产物来鉴定。结论:基于TaKaRa DEXPAT试剂盒的方法可检出少于10个分生孢子/样品。该方法可准确鉴定烟曲霉和黄曲霉,其他菌种可采用物种特异性探针或DNA测序进行鉴定。这些方法将为患者管理和未来的抗真菌和流行病学研究提供有价值的诊断工具。
Development of molecular methods for the identification of aspergillus and emerging moulds in paraffin wax embedded tissue sections.
Background/aims: Invasive infection with emerging moulds is increasing in incidence and reliable methods for speciating these organisms in tissue sections need to be developed.
Methods: Two methods for extracting fungal DNA from paraffin wax embedded tissue sections, based on the TaKaRa DEXPAT kit and QIAamp DNA mini kit, were optimised and compared. DNA was amplified by PCR using pan-fungal probes, and detected by Southern blot hybridisation using a high stringency method with a probe specific for Aspergillus fumigatus and A flavus.
Results: The method based on the TaKaRa DEXPAT kit, with additional steps using lyticase and ethanol precipitation, was superior. Less than 10 conidia were detectable using spiked samples and a positive result was obtained with 100% of clinical samples known to be culture positive for A fumigatus. Other moulds could be identified by using species specific probes or by sequencing PCR products.
Conclusions: The method based on the TaKaRa DEXPAT kit could detect less than 10 conidia/sample. The method allowed accurate identification of A fumigatus and A flavus and other species could be identified using species specific probes or by DNA sequencing. These methods will provide a valuable diagnostic tool for both patient management and future antifungal and epidemiological studies.