Section of Cariology, Department of Odontology, Umeå University, SE–901 87 Umeå, Sweden.
Caries Res. 2013;47(4):338-45. doi: 10.1159/000347233. Epub 2013 Mar 12.
This study assessed whether the persistence of Lactobacillus reuteri DSM 17938 and ATCC PTA 5289 in saliva could delay the regrowth of mutans streptococci (MS) after a full-mouth disinfection with chlorhexidine (CHX). A randomised, double-blind, placebo-controlled study with a 6-week intervention period and 3- and 6-month follow-up was performed. 62 healthy subjects with moderate to high counts of MS were randomly assigned to a test group (n = 32) or a placebo group (n = 30). Before onset of the intervention, subjects received two sessions of professional cleaning, flossing, and application of CHX varnish and rinsed their mouth with a CHX solution between the sessions (2 days). Thereafter, the test group used probiotic lozenges (2/day) containing L. reuteri (DSM 17938 and ATCC PTA 5289; 1 × 10(8) CFU of each strain), and the placebo group used identical lozenges lacking the lactobacilli. Saliva samples were collected and cultured onto selective media, and isolates of L. reuteri as well as DNA directly extracted from saliva were tested by polymerase chain reaction (PCR) with specific primers. Presence of salivary MS was analysed with a chair-side test. L. reuteri was frequently detected by culture during the intervention period but in only 3 test group subjects at follow-ups. Regrowth of MS statistically significantly differed depending on the presence or absence of L. reuteri DSM 17938 detected by PCR. We conclude that cultivable L. reuteri strains may only sporadically be confirmed after termination of the intervention, but subjects with PCR-detected L. reuteri demonstrated slower regrowth of MS.
本研究评估了罗伊氏乳杆菌 DSM 17938 和 ATCC PTA 5289 在唾液中的持续存在是否可以延缓氯己定(CHX)全口消毒后变形链球菌(MS)的再生。进行了一项随机、双盲、安慰剂对照研究,干预期为 6 周,随访期为 3 个月和 6 个月。62 名 MS 计数中度至高度的健康受试者被随机分配到试验组(n = 32)或安慰剂组(n = 30)。在干预开始前,受试者接受了两次专业清洁、牙线洁治和 CHX 牙漆应用,并在两次治疗之间用 CHX 溶液漱口(2 天)。此后,试验组使用含有罗伊氏乳杆菌(DSM 17938 和 ATCC PTA 5289;每种菌株 1×10(8)CFU)的益生菌含片(2/天),而安慰剂组使用不含乳杆菌的相同含片。收集唾液样本并在选择性培养基上培养,然后用聚合酶链反应(PCR)用特异性引物检测唾液中 L. reuteri 以及直接从唾液中提取的 DNA。使用椅旁试验分析唾液中 MS 的存在。在干预期间,通过培养经常检测到 L. reuteri,但在随访时仅在 3 名试验组受试者中检测到。MS 的再生与 PCR 检测到的 L. reuteri DSM 17938 的存在与否显著相关。我们的结论是,在干预结束后,可培养的 L. reuteri 菌株可能只是偶尔被证实,但通过 PCR 检测到 L. reuteri 的受试者 MS 的再生速度较慢。