Macdonald K, Cameron D W, Irungu G, D'Costa L J, Plummer F A, Slaney L A, Ndinya-Achola J O, Ronald A R
Department of Medicine, University of Manitoba, Winnipeg, Canada.
Sex Transm Dis. 1989 Apr-Jun;16(2):88-90. doi: 10.1097/00007435-198904000-00009.
Isolation of Haemophilus ducreyi is the only method for the definitive diagnosis of chancroid. Culture on supplemented gonococcal base (GCHgs) or on supplemented Muller-Hinton agar (MHHb) has yielded the best isolation rates. Sheffield media is an alternative to standard media. We compared the isolation rate of H. ducreyi on GCHgs and MHHb to that on the Sheffield media with and without 5% horse blood. Vancomycin (3 mg/L) was added to all media. Of the 87 specimens cultured from patients with genital ulcer disease, 57 (66%) were positive on either GCHgs or MHHb or on both. Twenty six (30%) were positive on GCHgs only, 15 (17%) on MHHb only, and 15 (17%) on both. One culture was positive on Sheffield medium with 5% horse blood; none were positive on Sheffield medium without horse blood. Stock strains showed good growth at 48 hr on GCHgs and MHHb, but no growth at 48 hr and only minimally detectable growth at 72 hr on Sheffield media with horse blood. No growth was detected on Sheffield media without horseblood. Thus optimal culture of H. ducreyi in Kenya requires two media, supplemented gonococcal base and Muller-Hinton agar. Sheffield media is not useful for the primary isolation of H. ducreyi.
分离杜克雷嗜血杆菌是软下疳确诊的唯一方法。在补充了营养成分的淋球菌培养基(GCHgs)或补充了营养成分的穆勒-欣顿琼脂(MHHb)上培养,分离率最高。谢菲尔德培养基是标准培养基的替代选择。我们比较了杜克雷嗜血杆菌在GCHgs、MHHb以及添加和未添加5%马血的谢菲尔德培养基上的分离率。所有培养基中均添加了万古霉素(3mg/L)。在87份取自生殖器溃疡疾病患者的培养标本中,57份(66%)在GCHgs或MHHb或两者上呈阳性。26份(30%)仅在GCHgs上呈阳性,15份(17%)仅在MHHb上呈阳性,15份(17%)在两者上均呈阳性。一份培养物在添加5%马血的谢菲尔德培养基上呈阳性;在未添加马血的谢菲尔德培养基上均未呈阳性。标准菌株在GCHgs和MHHb上于48小时生长良好,但在添加马血的谢菲尔德培养基上48小时无生长,72小时仅有微量可检测到的生长。在未添加马血的谢菲尔德培养基上未检测到生长。因此,在肯尼亚杜克雷嗜血杆菌的最佳培养需要两种培养基,即补充了营养成分的淋球菌培养基和穆勒-欣顿琼脂。谢菲尔德培养基对杜克雷嗜血杆菌的初次分离无用。