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Evaluation of lateral flow devices for identification of infected poultry by testing swab and feather specimens during H5N1 highly pathogenic avian influenza outbreaks in Vietnam

机译:通过在越南H5N1高致病性禽流感暴发中测试拭子和羽毛标本,评估侧向流动设备以鉴定受感染的家禽

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AbstractPlease cite this paper as: Slomka et al. (2012) Evaluation of lateral flow devices for identification of infected poultry by testing swab and feather specimens during H5N1 highly pathogenic avian influenza outbreaks in Vietnam. Influenza and Other Respiratory Viruses 6(5), 318–327.Background  Evaluation of two commercial lateral flow devices (LFDs) for avian influenza (AI) detection in H5N1 highly pathogenic AI infected poultry in Vietnam.Objectives  Determine sensitivity and specificity of the LFDs relative to a validated highly sensitive H5 RRT PCR.Methods  Swabs (cloacal and tracheal) and feathers were collected from 46 chickens and 48 ducks (282 clinical specimens) and tested by both LFDs and H5 RRT PCR. A subset of 59 chicken and 34 duck specimens was also tested by virus isolation (VI), the ‘gold standard’.Results  Twenty-six chickens and 15 ducks were shown to be infected by at least one RRT PCR positive clinical specimen per bird. Bird-level sensitivity for the Anigen LFD was 84·6% for chickens and 53·3% for ducks, and for the Quickvue LFD 65·4% for chickens and 33·3% for ducks. Comparison of the three clinical specimens revealed that chicken feathers were the most sensitive with 84% and 56% sensitivities for Anigen and Quickvue respectively. All 21 RRT PCR positive swabs from ducks were negative by both LFDs. However, duck feather testing gave sensitivities of 53·3% and 33·3% for Anigen and Quickvue respectively. Specificity was 100% for both LFDs in all investigations.Conclusions  Although LFDs were less sensitive than AI RRT PCR and VI, high titre viral shedding in H5N1 highly pathogenic avian influenza (HPAI) infected and diseased chickens is sufficient for a proportion of birds to be identified as AI infected by LFDs. Feathers were the optimal specimen for LFD testing in such diseased HPAI scenarios, particularly for ducks where swab testing by LFDs failed to identify any infected birds. However, specimens should be forwarded to the laboratory for confirmation by more sensitive diagnostic techniques.
机译:摘要请将此文引用为:Slomka等。 (2012)在越南H5N1高致病性禽流感暴发期间,通过测试拭子和羽毛标本评估侧向流动设备,以识别受感染的家禽。流感和其他呼吸道病毒6(5),318-327。背景技术评估越南用于H5N1高致病性AI感染家禽的两种商业侧向流动装置(LFD)的禽流感(AI)检测目的确定LFD的敏感性和特异性方法:从46只鸡和48只鸭子(282份临床标本)中收集拭子(泄殖腔和气管)和羽毛,并通过LFD和H5 RRT PCR进行测试。还通过“黄金标准”病毒分离(VI)测试了59个鸡和34个鸭标本的子集。结果:每只鸟至少有一个RRT PCR阳性临床标本被感染26只鸡和15只鸭。鸡对Anigen LFD的禽类敏感性为84·6%,对鸭子为53·3%,对Quickvue LFD对鸡为65·4%,对鸭子为33·3%。对这三个临床标本的比较显示,鸡羽毛对Anigen和Quickvue的敏感性最高,分别为84%和56%。两种LFD均检测出鸭的所有21个RRT PCR阳性拭子均为阴性。然而,鸭羽毛测试对Anigen和Quickvue的敏感性分别为53·3%和33·3%。在所有调查中,两种LFD的特异性均为100%。结论尽管LFD的敏感性不如AI RRT PCR和VI,但是在H5N1高致病性禽流感(HPAI)感染和患病的鸡中高滴度病毒脱落足以使一定比例的禽只被识别为被LFD感染的AI。在这种患病的高致病性禽流感情况下,羽毛是进行LFD测试的最佳标本,尤其是对于LFD进行拭子测试未能识别出任何感染禽鸟的鸭子而言。但是,应将标本送到实验室,以采用更灵敏的诊断技术进行确认。

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