The Nasopharyngeal Microbiota of Children With Respiratory Infections in Botswana

被引:35
作者
Kelly, Matthew S. [1 ,2 ]
Surette, Michael G. [3 ]
Smieja, Marek [4 ,5 ]
Pernica, Jeffrey M. [6 ]
Rossi, Laura [3 ]
Luinstra, Kathy [5 ]
Steenhoff, Andrew P. [1 ,7 ]
Feemster, Kristen A. [7 ,8 ]
Goldfarb, David M. [1 ,9 ]
Arscott-Mills, Tonya [1 ,7 ,8 ]
Boiditswe, Sefelani [1 ]
Rulaganyang, Ikanyeng [1 ]
Muthoga, Charles [1 ]
Gaofiwe, Letang [1 ]
Mazhani, Tiny [10 ]
Rawls, John F. [11 ]
Cunningham, Coleen K. [2 ]
Shah, Samir S. [12 ,13 ]
Seed, Patrick C. [2 ]
机构
[1] Botswana UPenn Partnership, Gaborone, Botswana
[2] Duke Univ, Med Ctr, Div Pediat Infect Dis, Box 3499, Durham, NC 27710 USA
[3] McMaster Univ, Dept Med, Hamilton, ON, Canada
[4] McMaster Univ, Dept Pathol & Mol Med, Hamilton, ON, Canada
[5] St Josephs Healthcare, Hamilton, ON, Canada
[6] McMaster Univ, Dept Pediat, Hamilton, ON, Canada
[7] Childrens Hosp Philadelphia, Global Hlth Ctr, Philadelphia, PA 19104 USA
[8] Childrens Hosp Philadelphia, Div Pediat Infect Dis, Philadelphia, PA 19104 USA
[9] BC Childrens Hosp, Dept Pathol & Lab Med, Vancouver, BC, Canada
[10] Univ Botswana, Sch Med, Gaborone, Botswana
[11] Duke Univ, Med Ctr, Dept Mol Genet & Microbiol, Ctr Genom Microbial Syst, Durham, NC USA
[12] Cincinnati Childrens Hosp Med Ctr, Div Hosp Med, Cincinnati, OH 45229 USA
[13] Cincinnati Childrens Hosp Med Ctr, Div Infect Dis, Cincinnati, OH 45229 USA
基金
美国国家卫生研究院;
关键词
microbiota; microbial communities; respiratory infections; pneumonia; children; HEALTHY-CHILDREN; PNEUMONIA; COMMUNITIES; INFANTS; DISEASE; ETIOLOGY; TRACT;
D O I
10.1097/INF.0000000000001607
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Background: Nearly half of child pneumonia deaths occur in sub-Saharan Africa. Microbial communities in the nasopharynx are a reservoir for pneumonia pathogens and remain poorly described in African children. Methods: Nasopharyngeal swabs were collected from children with pneumonia (N = 204), children with upper respiratory infection symptoms (N = 55) and healthy children (N = 60) in Botswana between April 2012 and April 2014. We sequenced the V3 region of the bacterial 16S ribosomal RNA gene and used partitioning around medoids to cluster samples into microbiota biotypes. We then used multivariable logistic regression to examine whether microbiota biotypes were associated with pneumonia and upper respiratory infection symptoms. Results: Mean ages of children with pneumonia, children with upper respiratory infection symptoms and healthy children were 8.2, 11.4 and 8.0 months, respectively. Clustering of nasopharyngeal microbiota identified 5 distinct biotypes: Corynebacterium/Dolosigranulum-dominant (23%), Haemophilus-dominant (11%), Moraxella-dominant (24%), Staphylococcus-dominant (13%) and Streptococcus-dominant (28%). The Haemophilus-dominant [odds ratio (OR): 13.55; 95% confidence interval (CI): 2.10-87.26], the Staphylococcus-dominant (OR: 8.27; 95% CI: 2.13-32.14) and the Streptococcus-dominant (OR: 39.97; 95% CI: 6.63-241.00) biotypes were associated with pneumonia. The Moraxella-dominant (OR: 3.71; 95% CI: 1.09-12.64) and Streptococcus-dominant (OR: 12.26; 95% CI: 1.81-83.06) biotypes were associated with upper respiratory infection symptoms. In children with pneumonia, HIV infection was associated with a lower relative abundance of Dolosigranulum (P = 0.03). Conclusions: Pneumonia and upper respiratory infection symptoms are associated with distinct nasopharyngeal microbiota biotypes in African children. A lower abundance of the commensal genus Dolosigranulum may contribute to the higher pneumonia risk of HIV-infected children.
引用
收藏
页码:E211 / E218
页数:8
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