Moriyama Kosei, Ando Chie, Tashiro Kosuke, Kuhara Satoru, Okamura Seiichi, Nakano Shuji, Takagi Yasumitsu, Miki Takeyoshi, Nakashima Yoshiyuki, Hirakawa Hideki
Nakamura Gakuen University, Faculty of Nutritional Sciences, Fukuoka, Japan.
Microbiol Immunol. 2008 Jul;52(7):375-82. doi: 10.1111/j.1348-0421.2008.00048.x.
Bacterial 16S ribosomal RNA genes (rDNA) were detected in blood samples from two healthy individuals by PCR under conditions involving 30 cycles that did not produce any visible products from negative control saline. Even from control samples, PCR involving 35-40 cycles yielded visible bands. Major clones detected in the blood samples, but not in control, were the Aquabacterium subgroup, Stenotrophomonas subgroup, Budvicia subgroup, Serratia subgroup, Bacillus subgroup and Flavobacteria subgroup. No clone was located within the bacteroides-clostridium-lactobacillus cluster, which is indigenous to gastrointestinal flora.
通过聚合酶链反应(PCR)在两名健康个体的血液样本中检测到细菌16S核糖体RNA基因(rDNA),该PCR条件为30个循环,在此条件下阴性对照生理盐水未产生任何可见产物。即使是对照样本,35 - 40个循环的PCR也产生了可见条带。在血液样本而非对照样本中检测到的主要克隆群包括水生杆菌亚群、嗜麦芽窄食单胞菌亚群、布戴维菌亚群、沙雷菌亚群、芽孢杆菌亚群和黄杆菌亚群。没有克隆位于胃肠道菌群特有的拟杆菌 - 梭菌 - 乳酸杆菌簇内。