Booton G C, Kelly D J, Chu Y-W, Seal D V, Houang E, Lam D S C, Byers T J, Fuerst P A
Department of Molecular Genetics, The Ohio State University, Columbus, OH 43210, USA.
J Clin Microbiol. 2002 May;40(5):1621-5. doi: 10.1128/JCM.40.5.1621-1625.2002.
We examined partial 18S ribosomal DNA (Rns) sequences of Acanthamoeba isolates cultured in a study of microbial keratitis in Hong Kong. Sequence differences were sufficient to distinguish closely related strains and were used to examine links between strains obtained from corneal scrape specimens, contact lenses, lens cases, lens case solutions, and home water-supply faucets of patients with Acanthamoeba. We also looked for evidence of mixed infections. Identification of Acanthamoeba Rns genotypes was based on sequences of approximately 113 bp within the genus-specific amplicon ASA.S1. This permitted genotype identification by using nonaxenic cultures. Of 13 specimens obtained from corneal scrapes, contact lenses, lens cases, or lens case solutions, 12 were Rns genotype T4 and the remaining one was Rns genotype T3. The sequences of corneal scrape specimens of two patients also were the same as those obtained from their contact lenses or lens case specimens. A possible triple-strain infection was indicated by three different T4 sequences in cultures from one patient's lenses. Although faucet water used by patients to clean their lenses is a possible source of infections, specimens isolated from the faucets at two Acanthamoeba keratitis patients' homes differed from their corneal scrape or lens specimens. The overall results demonstrate the potential of this Rns region for tracking Acanthamoeba keratitis strains in infections and for distinguishing single-strain and closely related multiple-strain infections even when other microorganisms might be present with the cultured specimens. They also confirm the predominance of Rns genotype T4 strains in Acanthamoeba keratitis infections.
我们检测了在香港一项微生物性角膜炎研究中培养的棘阿米巴分离株的部分18S核糖体DNA(Rns)序列。序列差异足以区分密切相关的菌株,并用于研究从角膜刮片标本、隐形眼镜、镜盒、镜盒溶液以及棘阿米巴患者家庭供水水龙头中获得的菌株之间的联系。我们还寻找了混合感染的证据。棘阿米巴Rns基因型的鉴定基于属特异性扩增子ASA.S1内约113 bp的序列。这使得通过使用非无菌培养物来鉴定基因型成为可能。从角膜刮片、隐形眼镜、镜盒或镜盒溶液中获得的13个标本中,12个为Rns基因型T4,其余1个为Rns基因型T3。两名患者角膜刮片标本的序列也与从他们的隐形眼镜或镜盒标本中获得的序列相同。一名患者镜片培养物中的三种不同T4序列表明可能存在三重菌株感染。尽管患者用于清洁镜片的水龙头水可能是感染源,但从两名棘阿米巴角膜炎患者家中的水龙头分离出的标本与他们的角膜刮片或镜片标本不同。总体结果表明,即使培养标本中可能存在其他微生物,该Rns区域在追踪棘阿米巴角膜炎感染菌株以及区分单菌株和密切相关的多菌株感染方面具有潜力。它们还证实了Rns基因型T4菌株在棘阿米巴角膜炎感染中的优势地位。