G. L. I. Santos, F. Burlandy, E. Costa, E. E. Silva
{"title":"巴西无菌性脑膜炎患者细胞培养阴性脑脊液中肠病毒基因组的直接检测","authors":"G. L. I. Santos, F. Burlandy, E. Costa, E. E. Silva","doi":"10.17525/VRR.V17I1-2.62","DOIUrl":null,"url":null,"abstract":"Enteroviruses are the main etiologic agents involved in outbreaks and sporadic cases of aseptic meningitis. Viral \nisolation in permissive cells is a traditional method for diagnosis, but it is time consuming and may be unsuccessful \ndue to low viral titers and because some enteroviruses do not replicate in routine cell cultures. Therefore, molecular \ntechniques are increasingly being used for detection of these agents. In the present work, 267 cerebrospinal fluid \n(CSF) samples from aseptic meningitis and meningoencephalitis cases, received between 2008 and 2009, were tested \nby RT-PCR. These clinical samples were previously negative for virus isolation in cell culture. Enterovirus genome \nwas detected in 59 CSF samples (22.1%) and identification was confirmed by partial nucleotide sequencing. Some \ndemographics of the patients included in the study were analyzed. Direct detection of enterovirus genome from CSF \nis appropriate to increase sensitivity in aseptic meningitis and meningoencephalitis cases.","PeriodicalId":30621,"journal":{"name":"Virus Reviews Research","volume":"17 1","pages":"8"},"PeriodicalIF":0.0000,"publicationDate":"2012-10-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"3","resultStr":"{\"title\":\"DIRECT DETECTION OF ENTEROVIRUS GENOME IN CELL-CULTURE NEGATIVE CEREBROSPINAL FLUID FROM ASEPTIC MENINGITIS CASES IN BRAZIL\",\"authors\":\"G. L. I. Santos, F. Burlandy, E. Costa, E. E. Silva\",\"doi\":\"10.17525/VRR.V17I1-2.62\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"Enteroviruses are the main etiologic agents involved in outbreaks and sporadic cases of aseptic meningitis. Viral \\nisolation in permissive cells is a traditional method for diagnosis, but it is time consuming and may be unsuccessful \\ndue to low viral titers and because some enteroviruses do not replicate in routine cell cultures. Therefore, molecular \\ntechniques are increasingly being used for detection of these agents. In the present work, 267 cerebrospinal fluid \\n(CSF) samples from aseptic meningitis and meningoencephalitis cases, received between 2008 and 2009, were tested \\nby RT-PCR. These clinical samples were previously negative for virus isolation in cell culture. Enterovirus genome \\nwas detected in 59 CSF samples (22.1%) and identification was confirmed by partial nucleotide sequencing. Some \\ndemographics of the patients included in the study were analyzed. Direct detection of enterovirus genome from CSF \\nis appropriate to increase sensitivity in aseptic meningitis and meningoencephalitis cases.\",\"PeriodicalId\":30621,\"journal\":{\"name\":\"Virus Reviews Research\",\"volume\":\"17 1\",\"pages\":\"8\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2012-10-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"3\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Virus Reviews Research\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.17525/VRR.V17I1-2.62\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Virus Reviews Research","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.17525/VRR.V17I1-2.62","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
DIRECT DETECTION OF ENTEROVIRUS GENOME IN CELL-CULTURE NEGATIVE CEREBROSPINAL FLUID FROM ASEPTIC MENINGITIS CASES IN BRAZIL
Enteroviruses are the main etiologic agents involved in outbreaks and sporadic cases of aseptic meningitis. Viral
isolation in permissive cells is a traditional method for diagnosis, but it is time consuming and may be unsuccessful
due to low viral titers and because some enteroviruses do not replicate in routine cell cultures. Therefore, molecular
techniques are increasingly being used for detection of these agents. In the present work, 267 cerebrospinal fluid
(CSF) samples from aseptic meningitis and meningoencephalitis cases, received between 2008 and 2009, were tested
by RT-PCR. These clinical samples were previously negative for virus isolation in cell culture. Enterovirus genome
was detected in 59 CSF samples (22.1%) and identification was confirmed by partial nucleotide sequencing. Some
demographics of the patients included in the study were analyzed. Direct detection of enterovirus genome from CSF
is appropriate to increase sensitivity in aseptic meningitis and meningoencephalitis cases.