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以FTA肝脏印记作为检测禽腺病毒和进行基因分型的DNA模板。

FTA liver impressions as DNA template for detecting and genotyping fowl adenovirus.

作者信息

Moscoso Hugo, Bruzual Jose J, Sellers Holly, Hofacre Charles L

机构信息

Poultry Diagnostic and Research Center, Department of Population Health, The University of Georgia, Athens, GA 30602-4875, USA.

出版信息

Avian Dis. 2007 Mar;51(1):118-21. doi: 10.1637/0005-2086(2007)051[0118:FLIADT]2.0.CO;2.

Abstract

The feasibility of using liver impressions on Flinders Technology Associates (FTA filter paper for the collection, inactivation, and molecular analysis of fowl adenovirus (FAV) was evaluated. FAV I European Union (EU) serotype 1 spotted on FTA was shown to be inactivated using specific-pathogen-free (SPF) primary chicken embryo liver cell culture as indicated by absence of cytopathic effect. Sensitivity of the polymerase chain reaction (PCR) test using tenfold dilutions of allantoic fluid from 100 to 10-4 for the detection of adenovirus serotype 1 on FTA cards was determined to be 0.0005 mean tissue culture infectious dose per FTA spot. The stability of the DNA from liver impressions on the FTA was found to be 198 days when stored at -20 degrees C. In a trial, inclusion body hepatitis (IBH) was experimentally reproduced in SPF chickens inoculated with FAV I EU serogroup 1, 4, 8, or 11, which presented weakness, pallor, depression, dehydration, and mortality within 6 days after inoculation. PCR performed on FTA liver impressions from the inoculated birds was able to detect all four viruses, and the nucleotide sequence analysis of the amplified PCR products (1219 bp of the hexone gene) revealed the expected serotypes. In addition to the trial, 55 clinical samples were analyzed from liver impressions on FTA cards, and FAV was detected in 11 of 55 (20%). Sequencing analysis showed that the viruses were EU serotypes 4, 5, 9, and 10. The results demonstrate that FTA filter paper inactivates the FAV I and maintains the DNA template for molecular analysis.

摘要

评估了使用弗林德斯技术协会(FTA)滤纸上的肝脏印记来收集、灭活和进行禽腺病毒(FAV)分子分析的可行性。如无细胞病变效应所示,在FTA上点样的FAV I欧盟(EU)1型血清型在无特定病原体(SPF)原代鸡胚肝细胞培养中被证明已被灭活。使用来自100到10⁻⁴的尿囊液十倍稀释液在FTA卡上检测腺病毒1型的聚合酶链反应(PCR)试验的灵敏度被确定为每个FTA点0.0005平均组织培养感染剂量。当在-20℃储存时,发现FTA上肝脏印记的DNA稳定性为198天。在一项试验中,用FAV I EU血清群1、4、8或11接种SPF鸡,实验性地再现了包涵体肝炎(IBH),接种后6天内出现虚弱、苍白、抑郁、脱水和死亡。对接种鸡的FTA肝脏印记进行的PCR能够检测到所有四种病毒,扩增的PCR产物(六邻体基因的1219 bp)的核苷酸序列分析揭示了预期的血清型。除了该试验外,还对FTA卡上肝脏印记的55份临床样本进行了分析,在55份样本中有11份(20%)检测到FAV。测序分析表明,这些病毒为EU血清型4、5、9和10。结果表明,FTA滤纸可灭活FAV I并维持用于分子分析的DNA模板。

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