Zinc influences innate and adaptive immune responses in mice with enterotoxigenic Escherichia coli-induced diarrhea

被引:0
|
作者
Yu, Jifeng [1 ,2 ]
Cao, Ye [1 ,2 ]
Xie, Jing [1 ,2 ]
Kang, Runmin [1 ,2 ]
Wei, Yong [1 ,2 ]
Ye, Yonggang [1 ,2 ]
Liao, Dangjin [1 ,2 ]
Li, Xingli [1 ,2 ]
Lin, Yi [1 ,2 ]
Dai, Zhuojian [1 ,2 ]
Pan, Meng [1 ,2 ]
Ye, Jianqiang [1 ,2 ]
机构
[1] Sichuan Anim Sci Acad, Inst Vet Med, Chengdu 610066, Sichuan, Peoples R China
[2] Key Lab Anim Genet & Breeding Sichuan Prov, 7 Niusha Rd, Chengdu 610066, Sichuan, Peoples R China
来源
INTERNATIONAL JOURNAL OF CLINICAL AND EXPERIMENTAL MEDICINE | 2018年 / 11卷 / 09期
关键词
Diarrhea; enterotoxigenic Escherichia coli; zinc deficiency; immune responses; DEVELOPING-COUNTRIES; VIRULENCE FACTORS; ORAL ZINC; DEFICIENCY; CHILDREN; MALNUTRITION; SUPPLEMENTATION; COLONIZATION; EPIDEMIOLOGY; INFECTION;
D O I
暂无
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
Enterotoxigenic Escherichia coli (ETEC) is a major cause of diarrheal disease. Information is limited on the effect of zinc on immune responses to diarrhea induced by ETEC. We investigated the immunological effects of zinc treatment in mice with diarrhea caused by ETEC. Our study included a total of 6 C57BL/6 mice aged 7-8 weeks that were treated with a high zinc diet for 2 weeks as well as 6 mice with ETEC-induced diarrhea that were not treated with zinc (UT). Six control mice (CON) of the same age group were also studied. The UT group showed more severe disruption to intestinal morphogenesis than ZT group. Serum zinc, complement C3, IgG, and IgM concentrations were higher in the ZT group than those in UT group but did not differ from those in the CON group. Phagocytic activity in mice in ZT group was greater than that in the UT group. However, oxidative burst capacity was lower in ZT group than in the UT group. The CD4/CD8 T-cell ratio in ZT group was higher than that in the UT group. Increased responses including complement C3, phagocytic activity, and changes in T-cell phenotypes suggests that zinc treatment enhances innate and adaptive immunity against ETEC infection in mice.
引用
收藏
页码:9248 / 9255
页数:8
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