Diarrhea in young children from low-income countries leads to large-scale alterations in intestinal microbiota composition

被引:181
作者
Pop, Mihai [1 ]
Walker, Alan W. [2 ]
Paulson, Joseph [1 ]
Lindsay, Brianna [3 ]
Antonio, Martin [4 ]
Hossain, M. Anowar [5 ]
Oundo, Joseph [6 ]
Tamboura, Boubou [7 ]
Mai, Volker
Astrovskaya, Irina [1 ]
Bravo, Hector Corrada [1 ]
Rance, Richard [2 ]
Stares, Mark [2 ]
Levine, Myron M. [3 ]
Panchalingam, Sandra [3 ]
Kotloff, Karen [3 ]
Ikumapayi, Usman N. [4 ]
Ebruke, Chinelo [4 ]
Adeyemi, Mitchell [4 ]
Ahmed, Dilruba [5 ]
Ahmed, Firoz [5 ]
Alam, Meer Taifur [5 ]
Amin, Ruhul [5 ]
Siddiqui, Sabbir [5 ]
Ochieng, John B. [6 ]
Ouma, Emmanuel [6 ]
Juma, Jane [6 ]
Mailu, Euince [6 ]
Omore, Richard [6 ]
Morris, J. Glenn [8 ]
Breiman, Robert F. [9 ]
Saha, Debasish [4 ]
Parkhill, Julian [2 ]
Nataro, James P. [10 ]
Stine, O. Colin [3 ]
机构
[1] Univ Maryland, College Pk, MD 20742 USA
[2] Wellcome Trust Sanger Inst, Hinxton, Cambs, England
[3] Univ Maryland, Sch Med, Baltimore, MD 21201 USA
[4] MRC Unit, Serrekunda, Gambia
[5] Int Ctr Diarrhoeal Dis Res, Dhaka 1000, Bangladesh
[6] Kenya Med Res Inst KEMRI, US Ctr Dis Control & Prevent Res Collaborat, Kisumu, Kenya
[7] Ctr Vaccine Dev, Bamako, Mali
[8] Univ Florida, Gainesville, FL USA
[9] Emory Univ, Atlanta, GA 30322 USA
[10] Univ Virginia, Charlottesville, VA USA
来源
GENOME BIOLOGY | 2014年 / 15卷 / 06期
基金
美国国家科学基金会; 英国惠康基金; 美国国家卫生研究院;
关键词
GLOBAL ENTERIC MULTICENTER; CLOSTRIDIUM-DIFFICILE; GUT MICROBIOTA; INFANTS; DIVERSITY; ETIOLOGY; DISEASE; GEMS; COMMUNITIES; STABILITY;
D O I
10.1186/gb-2014-15-6-r76
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Background: Diarrheal diseases continue to contribute significantly to morbidity and mortality in infants and young children in developing countries. There is an urgent need to better understand the contributions of novel, potentially uncultured, diarrheal pathogens to severe diarrheal disease, as well as distortions in normal gut microbiota composition that might facilitate severe disease. Results: We use high throughput 16S rRNA gene sequencing to compare fecal microbiota composition in children under five years of age who have been diagnosed with moderate to severe diarrhea (MSD) with the microbiota from diarrhea-free controls. Our study includes 992 children from four low-income countries in West and East Africa, and Southeast Asia. Known pathogens, as well as bacteria currently not considered as important diarrhea-causing pathogens, are positively associated with MSD, and these include Escherichia/Shigella, and Granulicatella species, and Streptococcus mitis/pneumoniae groups. In both cases and controls, there tend to be distinct negative correlations between facultative anaerobic lineages and obligate anaerobic lineages. Overall genus-level microbiota composition exhibit a shift in controls from low to high levels of Prevotella and in MSD cases from high to low levels of Escherichia/Shigella in younger versus older children; however, there was significant variation among many genera by both site and age. Conclusions: Our findings expand the current understanding of microbiota-associated diarrhea pathogenicity in young children from developing countries. Our findings are necessarily based on correlative analyses and must be further validated through epidemiological and molecular techniques.
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