Memish Ziad A, Al-Tawfiq Jaffar A, Makhdoom Hatem Q, Assiri Abdullah, Alhakeem Raafat F, Albarrak Ali, Alsubaie Sarah, Al-Rabeeah Abdullah A, Hajomar Waleed H, Hussain Raheela, Kheyami Ali M, Almutairi Abdullah, Azhar Esam I, Drosten Christian, Watson Simon J, Kellam Paul, Cotten Matthew, Zumla Alimuddin
Global Centre for Mass Gatherings Medicine and Ministry of Health, Riyadh, Kingdom of Saudi Arabia and College of Medicine, Alfaisal University.
Saudi Aramco Medical Services Organization, Dhahran Indiana University School of Medicine, Indianapolis.
J Infect Dis. 2014 Nov 15;210(10):1590-4. doi: 10.1093/infdis/jiu292. Epub 2014 May 15.
Analysis of clinical samples from patients with new viral infections is critical to confirm the diagnosis, to specify the viral load, and to sequence data necessary for characterizing the viral kinetics, transmission, and evolution. We analyzed samples from 112 patients infected with the recently discovered Middle East respiratory syndrome coronavirus (MERS-CoV).
Respiratory tract samples from cases of MERS-CoV infection confirmed by polymerase chain reaction (PCR) were investigated to determine the MERS-CoV load and fraction of the MERS-CoV genome. These values were analyzed to determine associations with clinical sample type.
Samples from 112 individuals in which MERS-CoV was detected by PCR were analyzed, of which 13 were sputum samples, 64 were nasopharyngeal swab specimens, 30 were tracheal aspirates, and 3 were bronchoalveolar lavage specimens; 2 samples were of unknown origin. Tracheal aspirates yielded significantly higher MERS-CoV loads, compared with nasopharyngeal swab specimens (P = .005) and sputum specimens (P = .0001). Tracheal aspirates had viral loads similar to those in bronchoalveolar lavage samples (P = .3079). Bronchoalveolar lavage samples and tracheal aspirates had significantly higher genome fraction than nasopharyngeal swab specimens (P = .0095 and P = .0002, respectively) and sputum samples (P = .0009 and P = .0001, respectively). The genome yield from tracheal aspirates and bronchoalveolar lavage samples were similar (P = .1174).
Lower respiratory tract samples yield significantly higher MERS-CoV loads and genome fractions than upper respiratory tract samples.
对新发病毒感染患者的临床样本进行分析,对于确诊、确定病毒载量以及获取表征病毒动力学、传播和进化所需的测序数据至关重要。我们分析了112例感染最近发现的中东呼吸综合征冠状病毒(MERS-CoV)患者的样本。
对经聚合酶链反应(PCR)确诊的MERS-CoV感染病例的呼吸道样本进行研究,以确定MERS-CoV载量和MERS-CoV基因组片段。分析这些数值以确定与临床样本类型的关联。
分析了112例经PCR检测出MERS-CoV的个体的样本,其中13份为痰样本,64份为鼻咽拭子标本,30份为气管吸出物,3份为支气管肺泡灌洗标本;2份样本来源不明。与鼻咽拭子标本(P = .005)和痰标本(P = .0001)相比,气管吸出物的MERS-CoV载量显著更高。气管吸出物的病毒载量与支气管肺泡灌洗样本相似(P = .3079)。支气管肺泡灌洗样本和气管吸出物的基因组片段比例显著高于鼻咽拭子标本(分别为P = .0095和P = .0002)和痰样本(分别为P = .0009和P = .0001)。气管吸出物和支气管肺泡灌洗样本的基因组产量相似(P = .1174)。
下呼吸道样本产生的MERS-CoV载量和基因组片段比例显著高于上呼吸道样本。