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一种低聚半乳糖产品可降低乳鼠轮状病毒感染率。

A Galactooligosaccharide Product Decreases the Rotavirus Infection in Suckling Rats.

作者信息

Massot-Cladera Malén, Rigo-Adrover María Del Mar, Herrero Laura, Franch Àngels, Castell Margarida, Vulevic Jelena, Pérez-Cano Francisco J, Lagunas María J Rodríguez

机构信息

Departament de Bioquímica i Fisiologia, Facultat de Farmàcia i Ciències de l'Alimentació, Universitat de Barcelona (UB), Av. Joan XXIII 27-31, 08028 Barcelona, Spain.

Institut de Recerca en Nutrició i Seguretat Alimentària (INSA), C/Prat de la Riba 171, 08921 Santa Coloma de Gramanet, Spain.

出版信息

Cells. 2022 May 18;11(10):1669. doi: 10.3390/cells11101669.

DOI:10.3390/cells11101669
PMID:35626706
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9139879/
Abstract

The leading cause of gastroenteritis among young children worldwide is the Group A rotaviruses (RV), which produce a wide range of symptoms, from a limited diarrhea to severe dehydration and even death. After an RV infection, immunity is not complete and less severe re-infections usually occur. These infections could be ameliorated by nutritional interventions with bioactive compounds, such as prebiotics. The aim of this research was to study the impact of a particular galactooligosaccharide (B-GOS) on the RV symptomatology and immune response during two consecutive infections. Lewis neonatal rats were inoculated with SA11 (first RV infection) on day 6 of life and with EDIM (second RV infection) on day 17 of life. B-GOS group was administered by oral gavage with a daily dose of B-GOS between days three to nine of life. Clinical and immunological variables were assessed during both infective processes. In the first infection, after the prebiotic intervention with B-GOS, a lower incidence, duration, and overall severity of the diarrhea (p < 0.05) was observed. In addition, it improved another severity indicator, the fecal weight output, during the diarrhea period (p < 0.05). The second RV infection failed in provoking diarrhea in the groups studied. The immune response during first infection with SA11 was not affected by B-GOS administration and had no impact on second infection, but the prebiotic intervention significantly increased IFN-γ and TNF-α intestinal production after the second infection (p < 0.05). In summary, B-GOS supplementation is able to reduce the incidence and severity of the RV-associated diarrhea and to influence the immune response against RV infections.

摘要

全球范围内,幼儿肠胃炎的主要病因是A组轮状病毒(RV),它会引发一系列症状,从轻微腹泻到严重脱水甚至死亡。感染RV后,免疫并不完全,通常会发生不太严重的再次感染。这些感染可以通过使用生物活性化合物(如益生元)进行营养干预来改善。本研究的目的是研究一种特定的低聚半乳糖(B-GOS)在连续两次感染期间对RV症状和免疫反应的影响。在出生第6天给新生Lewis大鼠接种SA11(第一次RV感染),在出生第17天接种EDIM(第二次RV感染)。在出生后第3天至第9天,通过口服灌胃给B-GOS组每日服用一剂B-GOS。在两个感染过程中评估临床和免疫变量。在第一次感染中,用B-GOS进行益生元干预后,观察到腹泻的发生率、持续时间和总体严重程度较低(p<0.05)。此外,它还改善了腹泻期间的另一个严重程度指标——粪便重量输出(p<0.05)。在研究的组中,第二次RV感染未引发腹泻。第一次感染SA11期间的免疫反应不受B-GOS给药的影响,对第二次感染也没有影响,但益生元干预在第二次感染后显著增加了肠道IFN-γ和TNF-α的产生(p<0.05)。总之,补充B-GOS能够降低RV相关腹泻的发生率和严重程度,并影响针对RV感染的免疫反应。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b81e/9139879/3b9c47989dbe/cells-11-01669-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b81e/9139879/b316c3ee229a/cells-11-01669-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b81e/9139879/1294ef912548/cells-11-01669-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b81e/9139879/5b85d3669913/cells-11-01669-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b81e/9139879/fca7901bfdcd/cells-11-01669-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b81e/9139879/0f73c78ee934/cells-11-01669-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b81e/9139879/3b9c47989dbe/cells-11-01669-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b81e/9139879/b316c3ee229a/cells-11-01669-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b81e/9139879/1294ef912548/cells-11-01669-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b81e/9139879/5b85d3669913/cells-11-01669-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b81e/9139879/fca7901bfdcd/cells-11-01669-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b81e/9139879/0f73c78ee934/cells-11-01669-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b81e/9139879/3b9c47989dbe/cells-11-01669-g006.jpg

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