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首页> 外文期刊>Clinical microbiology and infection: European Society of Clinical Microbiology and Infectious Diseases >Comparison of isolation rate of Borrelia burgdorferi sensu lato in two different culture media, MKP and BSK-H
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Comparison of isolation rate of Borrelia burgdorferi sensu lato in two different culture media, MKP and BSK-H

机译:两种不同培养基MKP和BSK-H上的疏螺旋疏螺旋体的分离率比较

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摘要

The aim of the study was to evaluate two culture media for Borrelia burgdorferi sensu lato isolation from a 5 × 2 × 2 mm skin biopsy that was dissected into two pieces and inoculated into modified Kelly-Pettenkofer (MKP) and Barbour-Stoenner-Kelly-H (BSK-H) medium. Samples were incubated at 33°C for up to 9 weeks. Borrelia species was determined by MluI-restriction of whole genome or by MseI-restriction of PCR product. We determined the proportion of isolation rate, 'slow-growers', contaminated specimens and Borrelia species in the two media. In each of the two media 235 skin specimens were cultivated. We found 90/470 (19.1%) contaminated cultures (BSK-H 67/235, 28.5%; MKP 23/235, 9.8%; p <0.0001). Borrelia growth was ascertained in 59/235 (25.1%) BSK-H and 102/235 (43.4%) MKP cultures (p <0.0001); the corresponding values for non-contaminated cultures were 59/168 (35.1%) and 102/212 (48.1%); (p 0.003). Fourteen specimens were positive only in BSK-H, 57 solely in MKP, and 43 in both culture media. Slow growth was present in 8/59 (13.6%) BSK-H and in 4/98 (4.1%) MKP positive cultures (p 0.019). Borrelia afzelii was identified in 44/51 (86.3%) BSK-H and in 88/98 (89.8%) MKP culture-positive samples; the corresponding findings for Boreelia garinii and B. burgdorferi sensu stricto were 6/51 (11.8%) and 9/98 (9.2%), and 1/51 (1.9%) and 1/98 (1.0%), for BSK-H and MKP, respectively. Comparison of MKP and BSK-H medium for Borrelia culturing from skin specimens of European patients with erythema migrans revealed the advantage of MKP over BSK-H. Clinical Microbiology and Infection
机译:该研究的目的是评估从5×2×2 mm皮肤活检中分离出的疏螺旋疏螺旋体的两种培养基,将其分为两部分并接种到改良的Kelly-Pettenkofer(MKP)和Barbour-Stoenner-Kelly- H(BSK-H)培养基。样品在33°C孵育9周。通过全基因组的MluI-限制性酶切或PCR产物的MseI-限制性酶切确定疏螺旋体种。我们确定了两种培养基中隔离率,“慢速生长者”,受污染的标本和疏螺旋体物种的比例。在两种培养基中的每一种中均培养了235个皮肤标本。我们发现90/470(19.1%)被污染的培养物(BSK-H 67/235,28.5%; MKP 23/235,9.8%; p <0.0001)。在59/235(25.1%)的BSK-H和102/235(43.4%)的MKP培养物中确定了疏螺旋体的生长(p <0.0001);非污染培养物的相应值为59/168(35.1%)和102/212(48.1%); (P = 0.003)。 14个标本仅在BSK-H中呈阳性,仅57个在MKP中呈阳性,在两种培养基中均为43个。在8/59(13.6%)BSK-H和4/98(4.1%)MKP阳性培养物中存在缓慢的生长(p = 0.019)。在44/51(86.3%)BSK-H和88/98(89.8%)MKP培养阳性样品中鉴定到非洲疏螺旋体; BSK-H的Boreelia garinii和B. burgdorferi sensu stricto的相应发现分别为6/51(11.8%)和9/98(9.2%),1/51(1.9%)和1/98(1.0%)和MKP。从欧洲偏头痛红斑患者皮肤样本中获得的疏螺旋体培养的MKP和BSK-H培养基的比较显示,MKP优于BSK-H。临床微生物学和感染

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