Moncla B J, Braham P, Hillier S L
Department of Periodontics, University of Washington, Seattle 98195.
J Clin Microbiol. 1990 Mar;28(3):422-5. doi: 10.1128/jcm.28.3.422-425.1990.
A filter paper spot test with 2'-(4-methylumbelliferyl)-alpha-D-N-acetylneuraminic acid as a substrate was used to study the prevalence of sialidase activity among gram-negative anaerobic and capnophilic bacteria. A total of 567 isolates representing four genera of obligate anaerobes and four genera of capnophilic organisms was tested. Sialidase activity was detected in 94% of 66 isolates from the Bacteroides fragilis group, 98% of 66 B. bivius isolates, and all isolates of the following species (number of isolates follows species name): B. capillosus, 4; B. levii, 2; B. denticola, 22; B. loescheii, 23; B. melaninogenicus, 32; B. forsythus, 44; and B. buccalis, 2. However, sialidase activity was detected in only 29% of 7 B. buccae isolates, 79% of 14 B. disiens isolates, and 55% of 11 B. oralis isolates. Sialidase activity was not detected among any of 13 isolates of B. gracilis, 12 isolates of B. ureolyticus, 61 isolates of B. intermedius, or 26 isolates of B. corporis. Porphyromonas (Bacteroides) asaccharolytica (20 isolates) and P. endodontalis (8 isolates) did not demonstrate sialidase activity, while 25 isolates of P. gingivalis were sialidase positive. Sialidase activity was found in 10 (100%) of 10 isolates of Capnocytophaga ochracea of C. sputigena but not in any of 4 C. gingivalis isolates. Other gram-negative anaerobic or capnophilic bacteria, including the following, were negative for sialidase activity: Fusobacterium nucleatum, 39 isolates; Wolinella recta, 19 isolates; Eikenella corrodens, 17 isolates; Haemophilus aphrophilus, 10 isolates; and Actinobacillus actinomycetemcomitans, 10 isolates. These data demonstrate sialidase activity in several species of the genera Bacteroides and Porphyromonas and suggest that this characteristic may be useful for identification.
以2'-(4-甲基伞形酮基)-α-D-N-乙酰神经氨酸为底物的滤纸斑点试验,用于研究革兰氏阴性厌氧菌和嗜二氧化碳菌中唾液酸酶活性的流行情况。共检测了代表四个专性厌氧菌属和四个嗜二氧化碳菌属的567株分离菌。在脆弱拟杆菌群的66株分离菌中有94%检测到唾液酸酶活性,66株双形拟杆菌分离菌中有98%检测到该活性,以下各菌种的所有分离菌(分离菌数量紧跟菌种名称之后)也检测到该活性:毛细拟杆菌,4株;利维拟杆菌,2株;龋齿拟杆菌,22株;洛氏拟杆菌,23株;产黑色素拟杆菌,32株;福赛斯坦纳菌,44株;颊拟杆菌,2株。然而,在7株颊拟杆菌分离菌中仅有29%检测到唾液酸酶活性,14株差异拟杆菌分离菌中有79%检测到该活性,11株口腔拟杆菌分离菌中有55%检测到该活性。在13株纤细拟杆菌、12株解脲拟杆菌、61株中间拟杆菌或26株人体拟杆菌的任何分离菌中均未检测到唾液酸酶活性。不解糖卟啉单胞菌(拟杆菌属)(20株分离菌)和牙髓卟啉单胞菌(8株分离菌)未显示唾液酸酶活性,而25株牙龈卟啉单胞菌分离菌唾液酸酶呈阳性。在10株黄褐二氧化碳嗜纤维菌或生痰二氧化碳嗜纤维菌分离菌中有10株(100%)检测到唾液酸酶活性,而4株牙龈二氧化碳嗜纤维菌分离菌中均未检测到该活性。其他革兰氏阴性厌氧菌或嗜二氧化碳菌,包括以下菌种,唾液酸酶活性均为阴性:具核梭杆菌,39株分离菌;直沃氏菌,19株分离菌;腐蚀艾肯菌,17株分离菌;嗜沫嗜血杆菌,10株分离菌;伴放线放线杆菌,10株分离菌。这些数据证明了拟杆菌属和卟啉单胞菌属几个菌种中存在唾液酸酶活性,并表明该特性可能有助于鉴定。