Case report: false-negative Xpert MRSA/SA BC result due to spa gene deletion in a patient with methicillin-resistant Staphylococcus aureus bacteremia

IF 1.5 4区 医学 Q3 INFECTIOUS DISEASES
Tatsuki Mura , Miyako Aso , Kae Kawamura , Kazumi Kanaya , Nobuhiko Ueda , Yoshitsugu Iinuma
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引用次数: 0

Abstract

Rapid diagnostic tests like the Xpert MRSA/SA BC assay are valuable for the early detection of Staphylococcus aureus (SA) and methicillin-resistant S. aureus (MRSA) in positive blood cultures. However, genetic variations in target regions can lead to false-negative results. We report a case of an 80's male with MRSA bacteremia where the Xpert MRSA/SA BC assay initially yielded false-negative results for both SA and MRSA. Subsequent culture confirmed MRSA, and whole-genome sequencing identified deletions within the spa gene, the target used for SA identification in the assay. This case highlights the importance of integrating molecular results with traditional culture methods, especially in cases of discordance, as genetic variants can impact the accuracy of rapid molecular assays.
病例报告:一例耐甲氧西林金黄色葡萄球菌菌血症患者因spa基因缺失导致Xpert MRSA/SA BC结果假阴性。
像Xpert MRSA/SA BC检测这样的快速诊断测试对于早期检测阳性血培养物中的金黄色葡萄球菌(SA)和耐甲氧西林金黄色葡萄球菌(MRSA)很有价值。然而,靶区的遗传变异可能导致假阴性结果。我们报告一例80年代男性MRSA菌血症病例,其中Xpert MRSA/SA BC检测最初对SA和MRSA均产生假阴性结果。随后的培养证实了MRSA,全基因组测序鉴定了spa基因中的缺失,spa基因是检测中用于SA鉴定的靶标。该病例强调了将分子结果与传统培养方法相结合的重要性,特别是在不一致的情况下,因为遗传变异会影响快速分子分析的准确性。
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来源期刊
Journal of Infection and Chemotherapy
Journal of Infection and Chemotherapy INFECTIOUS DISEASES-PHARMACOLOGY & PHARMACY
CiteScore
4.10
自引率
4.50%
发文量
303
审稿时长
47 days
期刊介绍: The Journal of Infection and Chemotherapy (JIC) — official journal of the Japanese Society of Chemotherapy and The Japanese Association for Infectious Diseases — welcomes original papers, laboratory or clinical, as well as case reports, notes, committee reports, surveillance and guidelines from all parts of the world on all aspects of chemotherapy, covering the pathogenesis, diagnosis, treatment, and control of infection, including treatment with anticancer drugs. Experimental studies on animal models and pharmacokinetics, and reports on epidemiology and clinical trials are particularly welcome.
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