Kawamura Yoshiaki, Kuwabara Saki, Kania Stephen A, Kato Hisayuki, Hamagishi Manami, Fujiwara Nagatoshi, Sato Takuichi, Tomida Junko, Tanaka Kaori, Bemis David A
Department of Microbiology, School of Pharmacy, Aichi Gakuin University, 1-100 Kusumoto-cho, Nagoya, Aichi 464-8650, Japan.
Department of Microbiology, School of Pharmacy, Aichi Gakuin University, 1-100 Kusumoto-cho, Nagoya, Aichi 464-8650, Japan.
Syst Appl Microbiol. 2015 Mar;38(2):104-9. doi: 10.1016/j.syapm.2014.11.004. Epub 2014 Nov 27.
During the process of identifying a Gram-negative coccobacillus isolated from a human clinical specimen, we found that the isolate's 16S rRNA gene had very close sequence identity with that of a variant Porphyromonas isolated from polymicrobial infections in the central bearded dragon, a species of lizard [2]. The 16S rRNA gene sequences of the human isolate and of six isolates from lizards were nearly identical (99.9-100%). Phylogenetic analysis placed all of these isolates in a single phylogenetic cluster well separated from other species in the genus Porphyromonas. The closest species was Porphyromonas catoniae with 90.7-90.9% sequence identity, although there was less than 6% DNA similarity between the P. catoniae type strain and our representative isolates from lizards (PAGU 1787(T)) and human (PAGU 1776). These isolates could grow under anaerobic or microaerobic conditions (6% O2 atmosphere). The isolates were positive for catalase and very strong β-hemolytic activity, but did not show black or brown pigmentation. Biochemically, the isolates could be differentiated from closely related species by pyroglutamic acid arylamidase and glycine arylamidase activity, and some others. The fermentation products mainly included succinic acid and propionic acid. The major fatty acids detected in cells of the isolates were iso-C15:0, anteiso-C15:0, and 3OH-iso-C17:0. The G+C content was 43.0 ± 0.62 mol%. The species name Porphyromonas pogonae sp. nov. is proposed for these isolates with the type strain of PAGU 1787(T) (=MI 10-1288(T)=JCM 19732(T)=ATCC BAA-2643(T)).
在鉴定从人类临床标本中分离出的革兰氏阴性球杆菌的过程中,我们发现该分离株的16S rRNA基因与从鬃狮蜥(一种蜥蜴)的多种微生物感染中分离出的变异卟啉单胞菌的16S rRNA基因具有非常接近的序列同一性[2]。人类分离株和来自蜥蜴的六个分离株的16S rRNA基因序列几乎相同(99.9 - 100%)。系统发育分析将所有这些分离株置于一个单一的系统发育簇中,与卟啉单胞菌属中的其他物种明显分开。最接近的物种是卡托尼亚卟啉单胞菌,序列同一性为90.7 - 90.9%,尽管卡托尼亚卟啉单胞菌模式菌株与我们从蜥蜴(PAGU 1787(T))和人类(PAGU 1776)中分离出的代表性菌株之间的DNA相似性低于6%。这些分离株可以在厌氧或微需氧条件下(6%氧气气氛)生长。分离株过氧化氢酶阳性且具有很强的β-溶血活性,但未显示黑色或棕色色素沉着。在生化方面,这些分离株可通过焦谷氨酸芳基酰胺酶和甘氨酸芳基酰胺酶活性等与密切相关的物种区分开来。发酵产物主要包括琥珀酸和丙酸。在分离株细胞中检测到的主要脂肪酸为异-C15:0、anteiso-C15:0和3OH-异-C17:0。G + C含量为43.0±0.62 mol%。提议将这些分离株命名为波氏卟啉单胞菌新种,模式菌株为PAGU 1787(T)(=MI 10 - 1288(T)=JCM 19732(T)=ATCC BAA - 2643(T))。