Droz S, Chi B, Horn E, Steigerwalt A G, Whitney A M, Brenner D J
Institute for Medical Microbiology, University of Berne, CH-3010 Berne, Switzerland.
J Clin Microbiol. 1999 Apr;37(4):1117-22. doi: 10.1128/JCM.37.4.1117-1122.1999.
Two of the 25 Bartonella isolates recovered during a prevalence study of Bartonella henselae bacteremia in domestic cats from the greater San Francisco Bay region were found to differ phenotypically and genotypically from all prior B. henselae isolates. These isolates, C-29 and C-30, which were recovered from the blood of two pet cats belonging to the same household, grew on chocolate agar as pinpoint colonies following 14 days of incubation at 35 degrees C in a candle jar but failed to grow on heart infusion agar supplemented with 5% rabbit blood. Additional phenotypic characteristics distinguished the isolates C-29 and C-30 from other feline B. henselae isolates. The restriction patterns obtained for C-29 and C-30 by citrate synthase PCR-restriction fragment length polymorphism (RFLP) analysis as well as by genomic RFLP could not be distinguished from each other but were distinctly different from that of the B. henselae type strain. In reciprocal reactions, DNAs from strains C-29 and C-30 were 97 to 100% related under optimal and stringent DNA reassociation conditions, with 0 to 0.5% divergence within related sequences. Labeled DNA from the type strain of B. henselae was 61 to 65% related to unlabeled DNAs from strains C-29 and C-30 in 55 degrees C reactions, with 5.0 to 5.5% divergence within the related sequences, and 31 to 41% related in stringent, 70 degrees C reactions. In reciprocal reactions, labeled DNAs from strains C-29 and C-30 were 68 to 92% related to those of the B. henselae type strain and other B. henselae strains, with 5 to 7% divergence. The 16S rRNA gene sequence of strain C-29 was 99.54% homologous to that of the type strain of B. henselae. On the basis of these findings, the two isolates C-29 and C-30 are designated a new species of Bartonella, for which we propose the name Bartonella koehlerae. The type strain of Bartonella koehlerae is strain C-29 (ATCC 700693).
在一项针对旧金山湾区家养猫亨氏巴尔通体菌血症的患病率研究中,从25株分离出的巴尔通体菌株中,有两株在表型和基因型上与之前所有的亨氏巴尔通体菌株都不同。这两株菌株C - 29和C - 30,是从同一家庭的两只宠物猫的血液中分离出来的,在烛缸中于35摄氏度孵育14天后,在巧克力琼脂上生长为针尖大小的菌落,但在添加了5%兔血的心脏浸液琼脂上无法生长。其他表型特征也将菌株C - 29和C - 30与其他猫源亨氏巴尔通体菌株区分开来。通过柠檬酸合酶PCR - 限制性片段长度多态性(RFLP)分析以及基因组RFLP获得的C - 29和C - 30的限制性图谱无法相互区分,但与亨氏巴尔通体模式菌株的图谱明显不同。在相互反应中,在最佳和严格的DNA重退火条件下,菌株C - 29和C - 30的DNA相关性为97%至100%,相关序列内的差异为0%至0.5%。在55摄氏度反应中,亨氏巴尔通体模式菌株的标记DNA与菌株C - 29和C - 30的未标记DNA的相关性为61%至65%,相关序列内的差异为5.0%至5.5%,在严格的70摄氏度反应中相关性为31%至41%。在相互反应中,菌株C - 29和C - 30的标记DNA与亨氏巴尔通体模式菌株和其他亨氏巴尔通体菌株的标记DNA的相关性为68%至92%,差异为5%至7%。菌株C - 29的16S rRNA基因序列与亨氏巴尔通体模式菌株的序列同源性为99.54%。基于这些发现,这两株菌株C - 29和C - 30被指定为巴尔通体的一个新物种,我们提议将其命名为科勒氏巴尔通体。科勒氏巴尔通体的模式菌株是菌株C - 29(ATCC 700693)。