Alcorn S M, Orum T V, Steigerwalt A G, Foster J L, Fogleman J C, Brenner D J
Department of Plant Pathology, University of Arizona, Tucson.
Int J Syst Bacteriol. 1991 Apr;41(2):197-212. doi: 10.1099/00207713-41-2-197.
A total of 108 pectolytic, soft-rotting Erwinia strains were collected from 11 types of cacti growing in Arizona, Texas, northern Mexico, and Australia between 1958 and 1989. Four strains were collected from soils beneath or close to naturally rotting saguaro cacti. Collectively, these strains caused soft rots of saguaro, organ pipe, and senita cacti, Opuntia (cactus) fruits and pads, tomato fruits, and potato slices, but only occasionally caused soft rots of slices of carrot roots. A numerical cluster analysis showed that 98 of the 112 strains formed a uniform group (cluster 1A) that was distinguished from other pectolytic erwinias by an API 20E code of 1205131, by negative reactions in API 50CHE tests for L-arabinose, myo-inositol, D-cellobiose, melibiose, and D-raffinose, and, in supplemental tests, by positive reactions for malonate and growth at 43 degrees C. The average levels of DNA relatedness of 22 cluster 1A strains to the proposed type strain (strain 1-12) as determined by the hydroxyapatite method were 88% in 60 degrees C reactions (with 1% divergence within related sequences) and 87% in 75 degrees C reactions. The levels of relatedness to the type strains of other Erwinia spp. were less than or equal to 38% in 75 degrees C reactions. Cluster 1A strains also had a characteristic cellular fatty acid profile containing cyclo-(11,12)-nonadecanoic acid (C19:0 Cyclo C11-12) and missing tridecanoic acid (C13:0), heptadecanoic acid (C17:0), and cis-9-heptadecenoic acid (C17:1 CIS 9), which separated them from other pectolytic erwinias. Collectively, these data indicate that the members of cluster 1A are members of a new species, which we name Erwinia cacticida. Three cactus strains in cluster 1B appear to represent a second new species that is closely related to E. cacticida; these strains are designated E. cacticida-like pending the availability of additional strains for testing. The remaining cactus strains (in cluster 4) have the physiological, DNA, and fatty acid profiles of Erwinia carotovora.
1958年至1989年间,从亚利桑那州、得克萨斯州、墨西哥北部和澳大利亚生长的11种仙人掌中总共收集了108株能产生果胶酶的软腐欧文氏菌菌株。其中4株是从自然腐烂的树形仙人掌下方或附近的土壤中收集的。这些菌株共同导致了树形仙人掌、管风琴仙人掌和Senita仙人掌、仙人掌果和仙人掌片、番茄果实以及土豆片的软腐,但只是偶尔会引起胡萝卜根切片的软腐。数值聚类分析表明,112株菌株中的98株形成了一个统一的组(聚类1A),通过API 20E编码1205131、在API 50CHE测试中对L-阿拉伯糖、肌醇、D-纤维二糖、蜜二糖和D-棉子糖呈阴性反应,以及在补充测试中对丙二酸呈阳性反应和在43℃下生长,该组与其他果胶分解欧文氏菌区分开来。通过羟基磷灰石法测定,22株聚类1A菌株与提议的模式菌株(菌株1-12)在60℃反应中的平均DNA相关性水平为88%(相关序列内差异为1%),在75℃反应中为87%。在75℃反应中,与其他欧文氏菌属模式菌株的相关性水平小于或等于38%。聚类1A菌株还具有独特的细胞脂肪酸谱,含有环(11,12)-十九烷酸(C19:0环C11-12),且缺少十三烷酸(C13:0)、十七烷酸(C17:0)和顺-9-十七碳烯酸(C17:1顺9),这使其与其他果胶分解欧文氏菌区分开来。总体而言,这些数据表明聚类1A的成员是一个新物种的成员,我们将其命名为仙人掌欧文氏菌。聚类1B中的三株仙人掌菌株似乎代表了与仙人掌欧文氏菌密切相关的第二个新物种;在有更多菌株可供测试之前,这些菌株被指定为类仙人掌欧文氏菌。其余的仙人掌菌株(在聚类4中)具有胡萝卜软腐欧文氏菌的生理、DNA和脂肪酸谱。