4.4 Article

Rapid identification of capsular serotype K1/K2 Klebsiella pneumoniae in pus samples from liver abscess patients and positive blood culture samples from bacteremia cases via an immunochromatographic strip assay

期刊

GUT PATHOGENS
卷 11, 期 -, 页码 -

出版社

BMC
DOI: 10.1186/s13099-019-0285-x

关键词

Klebsiella pneumoniae; Serotypes K1; Serotype K2; Serum agglutination; PCR; ICS

资金

  1. Tri-Service General Hospital
  2. National Defense Medical Center [TSGH-C105-115, TSGH-C106-095, MAB-105-11, MAB-106-80]

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BackgroundIn Asia, serotype K1/K2 Klebsiella pneumoniae are the major capsular serotypes that cause liver abscess or bacteremia in patients. The purpose of this study was to compare novel immunochromatographic strips (ICSs), which can rapidly detect K. pneumoniae serotypes K1/K2 in clinical samples, to conventional capsular serotyping methods.MethodsPus drainage samples from 16 patients with a liver abscess caused by K. pneumoniae, blood samples from 112 positive flagged blood culture bottle and a subsequent single colony in the medium were tested with the ICS. The results were then compared to findings of capsular swelling tests. Samples subjected to the polymerase chain reaction (PCR) analysis were used as reference.ResultsThe identification of K. pneumoniae via the traditional bacterial culture from pus samples took 3.4days on average (ranging from 2.2 to 5.5days). Further capsular serotyping of K. pneumoniae by the capsular swelling test of pure isolates lasted 5-10min, and the PCR method took 4h. As for ICSs, the time for direct identification of the K. pneumoniae capsular serotype K1/K2 in pus was<4min (ranging from 2 to 4min). The results of ICSs were consistent with capsular swelling tests and PCR methods. Testing of 112 blood culture samples and subsequent single colonies in the medium with ICSs yielded consistent results for most samples.ConclusionsThis study indicates that ICSs can rapidly detect K. pneumoniae serotypes K1 and K2 in pus or positive flagged blood culture broth samples within 5min. Their accuracy is comparable to that of the conventional capsular serotyping methods such as a serum agglutination assay or PCR.

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