Department of Paediatrics and Adolescent Medicine, Turku University Hospital and University of Turku, 20521, Turku, Finland.
Institute of Biomedicine, University of Turku and Clinical Microbiology, Turku University Hospital, Turku, Finland.
Eur J Clin Microbiol Infect Dis. 2020 Jul;39(7):1239-1244. doi: 10.1007/s10096-020-03836-5. Epub 2020 Feb 11.
Blood myxovirus resistance protein A (MxA) has broad antiviral activity, and it is a potential biomarker for symptomatic virus infections. Limited data is available of MxA in coinciding viral and bacterial infections. We investigated blood MxA levels in children hospitalized with a febrile urinary tract infection (UTI) with or without simultaneous respiratory virus infection. We conducted a prospective observational study of 43 children hospitalized with febrile UTI. Nasopharyngeal swab samples were collected at admission and tested for 16 respiratory viruses by nucleic acid detection methods. Respiratory symptoms were recorded, and blood MxA levels were determined. The median age of study children was 4 months (interquartile range, 2-14 months). A respiratory virus was detected in 17 (40%) children with febrile UTI. Of the virus-positive children with febrile UTI, 7 (41%) had simultaneous respiratory symptoms. Blood MxA levels were higher in virus-positive children with respiratory symptoms (median, 778 [interquartile range, 535-2538] μg/L) compared to either virus-negative (155 [94-301] μg/L, P < 0.001) or virus-positive (171 [112-331] μg/L, P = 0.006) children without respiratory symptoms at presentation with febrile UTI. MxA differentiated virus-positive children with respiratory symptoms from virus-negative without symptoms by an area under the receiver operating characteristic curve of 0.96. Respiratory viruses were frequently detected in children with febrile UTI. In UTI with simultaneous respiratory symptoms, host antiviral immune response was demonstrated by elevated blood MxA protein levels. MxA protein could be a robust biomarker of symptomatic viral infection in children with febrile UTI.
血液弹状病毒抗性蛋白 A(MxA)具有广泛的抗病毒活性,是症状性病毒感染的潜在生物标志物。同时合并病毒和细菌感染时,MxA 的相关数据有限。我们研究了同时合并呼吸道病毒感染的发热性尿路感染(UTI)患儿和无合并呼吸道病毒感染的发热性 UTI 患儿的血液 MxA 水平。我们进行了一项前瞻性观察性研究,纳入了 43 名因发热性 UTI 住院的患儿。入院时采集鼻咽拭子样本,采用核酸检测方法检测 16 种呼吸道病毒。记录呼吸道症状,并测定血液 MxA 水平。研究患儿的中位年龄为 4 个月(四分位距,2-14 个月)。发热性 UTI 患儿中 17 例(40%)检测到呼吸道病毒。发热性 UTI 病毒阳性患儿中,有 7 例(41%)同时存在呼吸道症状。有呼吸道症状的病毒阳性患儿的血液 MxA 水平更高(中位数,778[四分位距,535-2538]μg/L),与无呼吸道症状的病毒阴性患儿(155[94-301]μg/L,P<0.001)或病毒阳性患儿(171[112-331]μg/L,P=0.006)相比。MxA 对有呼吸道症状的病毒阳性患儿和无症状的病毒阴性患儿的区分能力通过受试者工作特征曲线下面积(area under the receiver operating characteristic curve,AUROC)达到 0.96。发热性 UTI 患儿中经常检测到呼吸道病毒。在同时合并呼吸道症状的 UTI 中,通过升高的血液 MxA 蛋白水平证实了宿主抗病毒免疫应答。MxA 蛋白可能是发热性 UTI 患儿症状性病毒感染的有力生物标志物。