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1
A diversity profile of the human skin microbiota.人类皮肤微生物群的多样性概况。
Genome Res. 2008 Jul;18(7):1043-50. doi: 10.1101/gr.075549.107. Epub 2008 May 23.
2
Diversity of the Lactobacillus group in breast milk and vagina of healthy women and potential role in the colonization of the infant gut.健康女性母乳和阴道中乳酸杆菌属的多样性及其在婴儿肠道定植中的潜在作用。
J Appl Microbiol. 2007 Dec;103(6):2638-44. doi: 10.1111/j.1365-2672.2007.03497.x.
3
Breast milk: a source of bifidobacteria for infant gut development and maturation?母乳:婴儿肠道发育和成熟过程中双歧杆菌的来源?
Neonatology. 2007;92(1):64-6. doi: 10.1159/000100088. Epub 2007 Feb 23.
4
Bacterial imprinting of the neonatal immune system: lessons from maternal cells?新生儿免疫系统的细菌印记:来自母体细胞的启示?
Pediatrics. 2007 Mar;119(3):e724-32. doi: 10.1542/peds.2006-1649.
5
Cultivation-independent assessment of the bacterial diversity of breast milk among healthy women.健康女性母乳细菌多样性的非培养评估
Res Microbiol. 2007 Jan-Feb;158(1):31-7. doi: 10.1016/j.resmic.2006.11.004. Epub 2006 Dec 19.
6
Response of the microaerophilic Bifidobacterium species, B. boum and B. thermophilum, to oxygen.微需氧双歧杆菌属的布氏双歧杆菌和嗜热双歧杆菌对氧气的反应。
Appl Environ Microbiol. 2006 Oct;72(10):6854-8. doi: 10.1128/AEM.01216-06. Epub 2006 Sep 1.
7
Molecular analysis of fungal microbiota in samples from healthy human skin and psoriatic lesions.来自健康人皮肤和银屑病皮损样本中真菌微生物群的分子分析。
J Clin Microbiol. 2006 Aug;44(8):2933-41. doi: 10.1128/JCM.00785-06.
8
Development of bacterial and bifidobacterial communities in feces of newborn babies.新生儿粪便中细菌和双歧杆菌群落的发育
Anaerobe. 2003 Oct;9(5):219-29. doi: 10.1016/j.anaerobe.2003.07.001.
9
Antimicrobial potential of four Lactobacillus strains isolated from breast milk.从母乳中分离出的四种乳酸杆菌菌株的抗菌潜力。
J Appl Microbiol. 2006 Jul;101(1):72-9. doi: 10.1111/j.1365-2672.2006.02981.x.
10
Distinct pattern of commensal gut microbiota in toddlers with eczema.患有湿疹的幼儿肠道共生微生物群的独特模式。
Int Arch Allergy Immunol. 2006;140(2):157-63. doi: 10.1159/000092555. Epub 2006 Apr 5.

从母乳中分离双歧杆菌,并通过聚合酶链反应-变性梯度凝胶电泳和定量实时聚合酶链反应评估双歧杆菌菌群。

Isolation of bifidobacteria from breast milk and assessment of the bifidobacterial population by PCR-denaturing gradient gel electrophoresis and quantitative real-time PCR.

作者信息

Martín Rocío, Jiménez Esther, Heilig Hans, Fernández Leonides, Marín María L, Zoetendal Erwin G, Rodríguez Juan M

机构信息

Laboratory of Microbiology, Wageningen University, Wageningen, The Netherlands.

出版信息

Appl Environ Microbiol. 2009 Feb;75(4):965-9. doi: 10.1128/AEM.02063-08. Epub 2008 Dec 16.

DOI:10.1128/AEM.02063-08
PMID:19088308
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2643565/
Abstract

The objective of this work was to elucidate if breast milk contains bifidobacteria and whether they can be transmitted to the infant gut through breastfeeding. Twenty-three women and their respective infants provided samples of breast milk and feces, respectively, at days 4 to 7 after birth. Gram-positive and catalase-negative isolates from specific media with typical bifidobacterial shapes were identified to the genus level by F6PPK (fructose-6-phosphate phosphoketolase) assays and to the species level by 16S rRNA gene sequencing. Bifidobacterial communities in breast milk were assessed by PCR-denaturing gradient gel electrophoresis (PCR-DGGE), and their levels were estimated by quantitative real-time PCR (qRTi-PCR). Bifidobacteria were present in 8 milk samples and 21 fecal samples. Bifidobacterium breve, B. adolescentis, and B. bifidum were isolated from milk samples, while infant feces also contained B. longum and B. pseudocatenulatum. PCR-DGGE revealed the presence of one to four dominant bifidobacterial bands in 22 milk samples. Sequences with similarities above 98% were identified as Bifidobacterium breve, B. adolescentis, B. longum, B. bifidum, and B. dentium. Bifidobacterial DNA was detected by qRTi-PCR in the same 22 milk samples at a range between 40 and 10,000 16S rRNA gene copies per ml. In conclusion, human milk seems to be a source of living bifidobacteria for the infant gut.

摘要

这项工作的目的是阐明母乳中是否含有双歧杆菌,以及它们能否通过母乳喂养传递到婴儿肠道。23名女性及其各自的婴儿在出生后第4至7天分别提供了母乳和粪便样本。通过F6PPK(6-磷酸果糖磷酸酮醇酶)测定将来自具有典型双歧杆菌形态的特定培养基的革兰氏阳性和过氧化氢酶阴性分离株鉴定到属水平,并通过16S rRNA基因测序鉴定到种水平。通过PCR-变性梯度凝胶电泳(PCR-DGGE)评估母乳中的双歧杆菌群落,并通过定量实时PCR(qRTi-PCR)估计其水平。在8份母乳样本和21份粪便样本中发现了双歧杆菌。从母乳样本中分离出短双歧杆菌、青春双歧杆菌和两歧双歧杆菌,而婴儿粪便中还含有长双歧杆菌和假链状双歧杆菌。PCR-DGGE显示22份母乳样本中存在一至四条主要的双歧杆菌条带。相似度高于98%的序列被鉴定为短双歧杆菌、青春双歧杆菌、长双歧杆菌、两歧双歧杆菌和龋齿双歧杆菌。通过qRTi-PCR在相同的22份母乳样本中检测到双歧杆菌DNA,每毫升的范围在40至10,000个16S rRNA基因拷贝之间。总之,母乳似乎是婴儿肠道中活双歧杆菌的一个来源。