Marconi R T, Liveris D, Schwartz I
Department of Microbiology and Immunology, Medical College of Virginia, Virginia Commonwealth University, Richmond 23298-0678, USA.
J Clin Microbiol. 1995 Sep;33(9):2427-34. doi: 10.1128/jcm.33.9.2427-2434.1995.
Borrelia spp. associated with Lyme disease possess an rRNA gene organization consisting of a single 16S rRNA gene followed by a spacer of several kilobases and a tandem repeat of a 23S (rrl)-5S (rrf) rRNA gene cluster. The restriction fragment length polymorphism (RFLP) patterns for these genes have been widely used to classify Lyme disease spirochete isolates. We analyzed the rRNA gene organization and sequences for two Ixodes ovatus isolates from Japan (IKA2 and HO14) and two group 21038 isolates associated with Ixodes dentatus ticks or rabbits from North America (isolates 21038 and 19857). This analysis revealed unique polymorphisms not previously described in other Lyme disease spirochete isolates. The molecular basis of these polymorphisms was determined by Southern blotting and PCR analyses. Only one continuous copy of the rrl-rrf gene cluster was identified in isolates IKA2, 19857, and 21038. The second rrl-rrf gene cluster is entirely absent from the IKA2 genome. In isolates 19857 and 21038, an intervening sequence is present, resulting in a fragment rrlB gene. The insertion site of this intervening sequence element differed in each isolate. While isolates 19857 and 21038 were found to carry a fragmented rrlB gene, they lacked rrfB. To determine if these rRNA polymorphisms were indicative of an underlying phylogenetic divergence, sequence analysis of the 16S rRNA (rrs) genes was conducted. The phylogenies inferred from rrs sequence analysis suggest that the polymorphisms resulted from recent mutational events. In addition, the phylogenetic analyses also support the proposed species status of Borrelia japonica sp. nov. and indicate that isolates of genomic group 21038 belong to a previously undescribed species for which we propose the nomenclature Borrelia andersonii sp. nov.
与莱姆病相关的疏螺旋体属具有一种核糖体RNA(rRNA)基因组织,其由单个16S rRNA基因、随后是几千碱基的间隔区以及一个23S(rrl)-5S(rrf)rRNA基因簇的串联重复组成。这些基因的限制性片段长度多态性(RFLP)模式已被广泛用于对莱姆病螺旋体分离株进行分类。我们分析了来自日本的两个卵形硬蜱分离株(IKA2和HO14)以及来自北美的与齿缘硬蜱或兔子相关的两个21038组分离株(分离株21038和19857)的rRNA基因组织和序列。该分析揭示了其他莱姆病螺旋体分离株中未曾描述过的独特多态性。通过Southern印迹和PCR分析确定了这些多态性的分子基础。在分离株IKA2、19857和21038中仅鉴定出一个连续的rrl - rrf基因簇拷贝。IKA2基因组中完全不存在第二个rrl - rrf基因簇。在分离株19857和21038中,存在一个插入序列,导致产生一个rrlB基因片段。该插入序列元件的插入位点在每个分离株中都不同。虽然发现分离株19857和21038携带一个片段化的rrlB基因,但它们缺乏rrfB。为了确定这些rRNA多态性是否指示潜在的系统发育分歧,对16S rRNA(rrs)基因进行了序列分析。从rrs序列分析推断的系统发育表明,这些多态性是由近期的突变事件导致的。此外,系统发育分析还支持日本疏螺旋体新种的提议物种地位,并表明基因组21038组的分离株属于一个先前未描述的物种,我们为此提议命名为安德森疏螺旋体新种。