H. Yoshioka, K. Fujita, H. Sakata, K. Murono, K. Iseki
{"title":"婴幼儿正常肠道菌群的发育及其临床意义","authors":"H. Yoshioka, K. Fujita, H. Sakata, K. Murono, K. Iseki","doi":"10.12938/BIFIDUS1982.10.1_11","DOIUrl":null,"url":null,"abstract":"We studied development of bacterial flora in the stool in breast-fed and bottlefed infants. Subjects and methods. Stools of 13 healthy newborn infants (six were breast-fed and seven were bottle-fed) were cultured. Stool samples were taken daily for six days after birth. Another culture was performed at one and three months of age, as the infants returned to the Well-Baby Clinic for a routine check-up. The stool was obtained directly from the rectum using a glass tube with rounded top and a side hole. The culture was performed within two hours of stool collection. A series of media were employed for anaerobic culture. Viande et de Levures medium with 0.2% glucose (VLG) was used for total bacterial count, VLG medium containing 7.5 ƒÊg/ml of vancomycin and 5 ƒÊg/ml of gentamicin for Bacteroides spp., and a modified Petuely's selective medium with nalidixic acid (MPN) was used for bifidobacteria (1). These media were prepared in test tubes with tight stoppers under \"pre-reduced anaerobically sterilized\" conditions. Procedures of anaerobic sample preparation and culture were performed by the method described by Holdeman et al (2). Air in the media and culture tubes was always substituted with CO2 using a CO2-gas stream. All cultures were done quantitatively and grown colonies were read and counted. Results. Changes in the count of organisms for individual bacterial groups are shown in Fig. 1 (3, 4). The count is described in terms of common logarithms of the bacterial count per g of feces (for example, a bacterial count of 108 per g of feces is expressed as log 8/g). On the day after birth, a mean organism total of log 9.0•}1.1/g of feces was measured. Enterobacteria were the predominant organism, followed by smaller numbers of enterococci, staphylococci, and Bacteroides. The number of entero-","PeriodicalId":414713,"journal":{"name":"Bifidobacteria and Microflora","volume":"21 1","pages":"0"},"PeriodicalIF":0.0000,"publicationDate":"1900-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"54","resultStr":"{\"title\":\"Development of the Normal Intestinal Flora and Clinical Significance in Infants and Children\",\"authors\":\"H. Yoshioka, K. Fujita, H. Sakata, K. Murono, K. Iseki\",\"doi\":\"10.12938/BIFIDUS1982.10.1_11\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"We studied development of bacterial flora in the stool in breast-fed and bottlefed infants. Subjects and methods. Stools of 13 healthy newborn infants (six were breast-fed and seven were bottle-fed) were cultured. Stool samples were taken daily for six days after birth. Another culture was performed at one and three months of age, as the infants returned to the Well-Baby Clinic for a routine check-up. The stool was obtained directly from the rectum using a glass tube with rounded top and a side hole. The culture was performed within two hours of stool collection. A series of media were employed for anaerobic culture. Viande et de Levures medium with 0.2% glucose (VLG) was used for total bacterial count, VLG medium containing 7.5 ƒÊg/ml of vancomycin and 5 ƒÊg/ml of gentamicin for Bacteroides spp., and a modified Petuely's selective medium with nalidixic acid (MPN) was used for bifidobacteria (1). These media were prepared in test tubes with tight stoppers under \\\"pre-reduced anaerobically sterilized\\\" conditions. Procedures of anaerobic sample preparation and culture were performed by the method described by Holdeman et al (2). Air in the media and culture tubes was always substituted with CO2 using a CO2-gas stream. All cultures were done quantitatively and grown colonies were read and counted. Results. Changes in the count of organisms for individual bacterial groups are shown in Fig. 1 (3, 4). The count is described in terms of common logarithms of the bacterial count per g of feces (for example, a bacterial count of 108 per g of feces is expressed as log 8/g). On the day after birth, a mean organism total of log 9.0•}1.1/g of feces was measured. Enterobacteria were the predominant organism, followed by smaller numbers of enterococci, staphylococci, and Bacteroides. 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引用次数: 54
摘要
我们研究了母乳喂养和奶瓶喂养婴儿粪便中细菌菌群的发育。研究对象和方法。对13名健康新生儿(6名母乳喂养,7名奶瓶喂养)的粪便进行了培养。出生后6天每天采集粪便样本。另一种培养是在婴儿1个月和3个月大时进行的,当婴儿回到Well-Baby诊所进行常规检查时。粪便是直接从直肠获得的,使用一个圆形顶部和侧孔的玻璃管。粪便收集后两小时内进行培养。采用一系列培养基进行厌氧培养。细菌总数用含有0.2%葡萄糖的Viande et de Levures培养基(VLG),拟杆菌用含有7.5 ƒÊg/ml万古霉素和5 ƒÊg/ml庆大霉素的VLG培养基,双歧杆菌用含有纳利迪酸(MPN)的改良Petuely选择性培养基(1)。这些培养基在“预还原厌氧灭菌”条件下,在带密封塞的试管中制备。厌氧样品制备和培养过程由Holdeman等人(2)描述的方法进行。培养基和培养管中的空气总是用CO2-气体流代替CO2。所有的培养都是定量的,生长的菌落被读取和计数。结果。单个细菌群的微生物数量变化如图1(3,4)所示。计数以每克粪便中细菌数量的常用对数来描述(例如,每克粪便中细菌数量为108,表示为log 8/g)。出生后第1天,测定粪便中平均微生物总数为log 9.0•}1.1/g。以肠杆菌为主,其次是数量较少的肠球菌、葡萄球菌和拟杆菌。进入的数量
Development of the Normal Intestinal Flora and Clinical Significance in Infants and Children
We studied development of bacterial flora in the stool in breast-fed and bottlefed infants. Subjects and methods. Stools of 13 healthy newborn infants (six were breast-fed and seven were bottle-fed) were cultured. Stool samples were taken daily for six days after birth. Another culture was performed at one and three months of age, as the infants returned to the Well-Baby Clinic for a routine check-up. The stool was obtained directly from the rectum using a glass tube with rounded top and a side hole. The culture was performed within two hours of stool collection. A series of media were employed for anaerobic culture. Viande et de Levures medium with 0.2% glucose (VLG) was used for total bacterial count, VLG medium containing 7.5 ƒÊg/ml of vancomycin and 5 ƒÊg/ml of gentamicin for Bacteroides spp., and a modified Petuely's selective medium with nalidixic acid (MPN) was used for bifidobacteria (1). These media were prepared in test tubes with tight stoppers under "pre-reduced anaerobically sterilized" conditions. Procedures of anaerobic sample preparation and culture were performed by the method described by Holdeman et al (2). Air in the media and culture tubes was always substituted with CO2 using a CO2-gas stream. All cultures were done quantitatively and grown colonies were read and counted. Results. Changes in the count of organisms for individual bacterial groups are shown in Fig. 1 (3, 4). The count is described in terms of common logarithms of the bacterial count per g of feces (for example, a bacterial count of 108 per g of feces is expressed as log 8/g). On the day after birth, a mean organism total of log 9.0•}1.1/g of feces was measured. Enterobacteria were the predominant organism, followed by smaller numbers of enterococci, staphylococci, and Bacteroides. The number of entero-