Tze Shien Lo , Michihiko Goto , Kimberly D.P. Hammer
{"title":"以 Vitek 2 抗菌药敏感性测试卡系统为参照标准,评估 Alere PBP2a SA 培养菌落测试仪在凝固酶阴性葡萄球菌中的性能","authors":"Tze Shien Lo , Michihiko Goto , Kimberly D.P. Hammer","doi":"10.1016/j.imj.2024.100126","DOIUrl":null,"url":null,"abstract":"<div><h3>Background</h3><p>The Alere PBP2a SA Culture Colony Test is an FDA-cleared <em>in vitro</em> immunochromatographic assay for rapid detection of penicillin-binding protein2a (PBP2a) in <em>Staphylococcus aureus</em>.</p></div><div><h3>Methods</h3><p>We investigated the performance of the PBP2a SA Culture Colony Test with 78 coagulase-negative <em>Staphylococcus</em> (CoNS) isolates from different body sites, with the Vitek 2 Antimicrobial Susceptibility Test (AST) as a reference standard.</p></div><div><h3>Results</h3><p>The CoNS species were 62 <em>S. epidermidis</em>; 6 <em>S. lugdenensis</em>; 3 <em>S. hominis</em>; 2 <em>S. capitis</em>; 2 <em>S. haemolyticus</em>; and 1 each of <em>S. simulans, S. auricularis,</em> and <em>S. warneri</em>. Of the 78 CoNS isolates, 68 showed concordance in the PBP2a IC assay and Vitek 2 AST. Discordance was seen for 10 <em>S. epidermidis</em> isolates, which showed negative in the PBP2a assay, despite oxacillin-resistance detection using the Vitek 2 AST (66.7% sensitivity and 100% specificity). All non-<em>S. epidermidis</em> CoNS were identified with 100% concordance using the PBP2a IC assay and Vitek 2 AST.</p></div><div><h3>Conclusion</h3><p>We demonstrated that, while the PBP2a IC assay has low sensitivity in determining the susceptibility of <em>S. epidermidis</em> to oxacillin, it highly accurately predicted the susceptibility of non-<em>S. epidermidis</em> CoNS to oxacillin. The diagnostic accuracy for non-<em>S. epidermidis</em> CoNS needs further assessment with more isolates to confirm our findings.</p></div>","PeriodicalId":100667,"journal":{"name":"Infectious Medicine","volume":"3 3","pages":"Article 100126"},"PeriodicalIF":0.0000,"publicationDate":"2024-09-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.sciencedirect.com/science/article/pii/S2772431X24000406/pdfft?md5=5e42b688ea687e5e6b0098af695bcbc1&pid=1-s2.0-S2772431X24000406-main.pdf","citationCount":"0","resultStr":"{\"title\":\"Evaluating the performance of the Alere PBP2a SA Culture Colony Test with the Vitek 2 Antimicrobial Susceptibility Test Card System as reference standard in coagulase-negative Staphylococcus species\",\"authors\":\"Tze Shien Lo , Michihiko Goto , Kimberly D.P. Hammer\",\"doi\":\"10.1016/j.imj.2024.100126\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><h3>Background</h3><p>The Alere PBP2a SA Culture Colony Test is an FDA-cleared <em>in vitro</em> immunochromatographic assay for rapid detection of penicillin-binding protein2a (PBP2a) in <em>Staphylococcus aureus</em>.</p></div><div><h3>Methods</h3><p>We investigated the performance of the PBP2a SA Culture Colony Test with 78 coagulase-negative <em>Staphylococcus</em> (CoNS) isolates from different body sites, with the Vitek 2 Antimicrobial Susceptibility Test (AST) as a reference standard.</p></div><div><h3>Results</h3><p>The CoNS species were 62 <em>S. epidermidis</em>; 6 <em>S. lugdenensis</em>; 3 <em>S. hominis</em>; 2 <em>S. capitis</em>; 2 <em>S. haemolyticus</em>; and 1 each of <em>S. simulans, S. auricularis,</em> and <em>S. warneri</em>. Of the 78 CoNS isolates, 68 showed concordance in the PBP2a IC assay and Vitek 2 AST. Discordance was seen for 10 <em>S. epidermidis</em> isolates, which showed negative in the PBP2a assay, despite oxacillin-resistance detection using the Vitek 2 AST (66.7% sensitivity and 100% specificity). All non-<em>S. epidermidis</em> CoNS were identified with 100% concordance using the PBP2a IC assay and Vitek 2 AST.</p></div><div><h3>Conclusion</h3><p>We demonstrated that, while the PBP2a IC assay has low sensitivity in determining the susceptibility of <em>S. epidermidis</em> to oxacillin, it highly accurately predicted the susceptibility of non-<em>S. epidermidis</em> CoNS to oxacillin. The diagnostic accuracy for non-<em>S. epidermidis</em> CoNS needs further assessment with more isolates to confirm our findings.</p></div>\",\"PeriodicalId\":100667,\"journal\":{\"name\":\"Infectious Medicine\",\"volume\":\"3 3\",\"pages\":\"Article 100126\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2024-09-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://www.sciencedirect.com/science/article/pii/S2772431X24000406/pdfft?md5=5e42b688ea687e5e6b0098af695bcbc1&pid=1-s2.0-S2772431X24000406-main.pdf\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Infectious Medicine\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://www.sciencedirect.com/science/article/pii/S2772431X24000406\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Infectious Medicine","FirstCategoryId":"1085","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S2772431X24000406","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
Evaluating the performance of the Alere PBP2a SA Culture Colony Test with the Vitek 2 Antimicrobial Susceptibility Test Card System as reference standard in coagulase-negative Staphylococcus species
Background
The Alere PBP2a SA Culture Colony Test is an FDA-cleared in vitro immunochromatographic assay for rapid detection of penicillin-binding protein2a (PBP2a) in Staphylococcus aureus.
Methods
We investigated the performance of the PBP2a SA Culture Colony Test with 78 coagulase-negative Staphylococcus (CoNS) isolates from different body sites, with the Vitek 2 Antimicrobial Susceptibility Test (AST) as a reference standard.
Results
The CoNS species were 62 S. epidermidis; 6 S. lugdenensis; 3 S. hominis; 2 S. capitis; 2 S. haemolyticus; and 1 each of S. simulans, S. auricularis, and S. warneri. Of the 78 CoNS isolates, 68 showed concordance in the PBP2a IC assay and Vitek 2 AST. Discordance was seen for 10 S. epidermidis isolates, which showed negative in the PBP2a assay, despite oxacillin-resistance detection using the Vitek 2 AST (66.7% sensitivity and 100% specificity). All non-S. epidermidis CoNS were identified with 100% concordance using the PBP2a IC assay and Vitek 2 AST.
Conclusion
We demonstrated that, while the PBP2a IC assay has low sensitivity in determining the susceptibility of S. epidermidis to oxacillin, it highly accurately predicted the susceptibility of non-S. epidermidis CoNS to oxacillin. The diagnostic accuracy for non-S. epidermidis CoNS needs further assessment with more isolates to confirm our findings.