Bosley G S, Whitney A M, Pruckler J M, Moss C W, Daneshvar M, Sih T, Talkington D F
Division of Bacterial and Mycotic Diseases, Centers for Disease Control and Prevention, Atlanta, Georgia, USA.
J Clin Microbiol. 1995 Nov;33(11):2876-80. doi: 10.1128/jcm.33.11.2876-2880.1995.
Nineteen isolates of Alloiococcus otitidis from ear fluid samples collected by tympanostomy from patients at four geographic locations were identified by phenotypic characterization and genetic relatedness. Initial growth of A. otitidis isolates occurred after 3 days at 37 degrees C on brain heart infusion (BHI) agar with 5% rabbit blood. Heavy growth occurred in BHI broth supplemented with 0.07% lecithin and 0.5% Tween 80 after 4 days of incubation. The isolates were gram-positive cocci that divided on an irregular plane and produced metabolic lactic acid, pyrrolidonyl arylamidase, and leucine aminopeptidase. These cocci grew sparsely in 6.5% NaCl-BHI broth, were asaccharolytic on both fermentative and oxidative bases, and were cytochrome negative by the iron-porphyrin test. The cellular fatty acid profile of A. otitidis was distinguished from those of related genera and characterized by major amounts ( > or = 14%) of 16:0, 18:2, 18:1 omega 9c, and 18:0 and smaller amounts of 14:0, 16:1 omega 7c, 17:0, and 18:1 omega 7c. Fifteen isolates demonstrated > 69% relatedness by DNA-DNA hybridization. Four isolates plus the original 15 were confirmed as A. otitidis by dot blot hybridization with a digoxigenin-labeled nucleotide probe specific for this species. The intergenic space between the genes coding for the 16S and 23S rRNAs of alloiococci was amplified by PCR, analyzed by restriction fragment length polymorphism, and determined to consist of three different genetic types. Although beta-lactamase negative, A. otitidis demonstrated intermediate levels of resistance to beta-lactams, including expanded-spectrum cephalosporins, and were resistant to trimethoprim-sulfamethoxazole and erythromycin.
通过表型特征和遗传相关性鉴定了从四个地理位置的患者经鼓膜造孔术采集的耳液样本中分离出的19株耳炎差异球菌。耳炎差异球菌分离株在37℃、含5%兔血的脑心浸液(BHI)琼脂上培养3天后开始初步生长。在添加0.07%卵磷脂和0.5%吐温80的BHI肉汤中培养4天后大量生长。这些分离株为革兰氏阳性球菌,在不规则平面上分裂,产生代谢乳酸、吡咯烷酮芳基酰胺酶和亮氨酸氨肽酶。这些球菌在6.5%NaCl - BHI肉汤中生长稀疏,在发酵和氧化基础上均不产糖,铁卟啉试验显示细胞色素阴性。耳炎差异球菌的细胞脂肪酸谱与相关属的不同,其特征是主要含有大量(≥14%)的16:0、18:2、18:1 ω9c和18:0,少量含有14:0、16:1 ω7c、17:0和18:1 ω7c。通过DNA - DNA杂交,15株分离株显示出>69%的相关性。通过与针对该物种的地高辛标记核苷酸探针进行斑点印迹杂交,另外4株分离株以及最初的15株被确认为耳炎差异球菌。通过PCR扩增了耳炎差异球菌编码16S和23S rRNA的基因之间的基因间隔区,通过限制性片段长度多态性分析,确定其由三种不同的遗传类型组成。尽管耳炎差异球菌β-内酰胺酶阴性,但对包括超广谱头孢菌素在内的β-内酰胺类药物表现出中等水平的耐药性,并且对甲氧苄啶-磺胺甲恶唑和红霉素耐药。