Late-Onset Bloodstream Infection and Perturbed Maturation of the Gastrointestinal Microbiota in Premature Infants

被引:85
作者
Shaw, Alexander G. [1 ]
Sim, Kathleen [1 ]
Randell, Paul [1 ]
Cox, Michael J. [2 ]
McClure, Zoe E. [1 ]
Li, Ming-Shi [1 ]
Donaldson, Hugo [3 ]
Langford, Paul R. [1 ]
Cookson, William O. C. M. [2 ]
Moffatt, Miriam F. [2 ]
Kroll, J. Simon [1 ]
机构
[1] Univ London Imperial Coll Sci Technol & Med, Dept Med, Paediat Sect, London, England
[2] Univ London Imperial Coll Sci Technol & Med, Natl Heart & Lung Inst, Dept Mol Genet & Genom, London, England
[3] NHS Trust, Imperial Coll, Dept Microbiol, London, England
来源
PLOS ONE | 2015年 / 10卷 / 07期
基金
美国国家卫生研究院; 英国惠康基金;
关键词
BIRTH-WEIGHT INFANTS; SEPSIS; GUT; TRANSLOCATION; POPULATIONS; DIAGNOSIS;
D O I
10.1371/journal.pone.0132923
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Background Late-onset bloodstream infection (LO-BSI) is a common complication of prematurity, and lack of timely diagnosis and treatment can have life-threatening consequences. We sought to identify clinical characteristics and microbial signatures in the gastrointestinal microbiota preceding diagnosis of LO-BSI in premature infants. Method Daily faecal samples and clinical data were collected over two years from 369 premature neonates (<32 weeks gestation). We analysed samples from 22 neonates who developed LO-BSI and 44 matched control infants. Next-generation sequencing of 16S rRNA gene regions amplified by PCR from total faecal DNA was used to characterise the microbiota of faecal samples preceding diagnosis from infants with LO-BSI and controls. Culture of selected samples was undertaken, and bacterial isolates identified using MALDI-TOF. Antibiograms from bloodstream and faecal isolates were compared to explore strain similarity. Results From the week prior to diagnosis, infants with LO-BSI had higher proportions of faecal aerobes/facultative anaerobes compared to controls. Risk factors for LO-BSI were identified by multivariate analysis. Enterobacteriaceal sepsis was associated with antecedent multiple lines, low birth weight and a faecal microbiota with prominent Enterobacteriaceae. Staphylococcal sepsis was associated with Staphylococcus OTU faecal over-abundance, and the number of days prior to diagnosis of mechanical ventilation and of the presence of centrally-placed lines. In 12 cases, the antibiogram of the bloodstream isolate matched that of a component of the faecal microbiota in the sample collected closest to diagnosis. Conclusions The gastrointestinal tract is an important reservoir for LO-BSI organisms, pathogens translocating across the epithelial barrier. LO-BSI is associated with an aberrant microbiota, with abundant staphylococci and Enterobacteriaceae and a failure to mature towards predominance of obligate anaerobes.
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共 42 条
[1]  
[Anonymous], MAN OP 2
[2]  
[Anonymous], BSAC METH ANT SUSC T
[3]   Establishment and development of intestinal microbiota in preterm neonates [J].
Arboleya, Silvia ;
Binetti, Ana ;
Salazar, Nuria ;
Fernandez, Nuria ;
Solis, Gonzalo ;
Hernandez-Barranco, Ana ;
Margolles, Abelardo ;
de los Reyes-Gavilan, Clara G. ;
Gueimonde, Miguel .
FEMS MICROBIOLOGY ECOLOGY, 2012, 79 (03) :763-772
[4]   Serial serum C-reactive protein levels in the diagnosis of neonatal infection [J].
Benitz, WE ;
Han, MY ;
Madan, A ;
Ramachandra, P .
PEDIATRICS, 1998, 102 (04) :E41
[5]   Late-Onset Sepsis in Very Low Birth Weight Infants from Singleton and Multiple-Gestation Births [J].
Boghossian, Nansi S. ;
Page, Grier P. ;
Bell, Edward F. ;
Stoll, Barbara J. ;
Murray, Jeffrey C. ;
Cotten, C. Michael ;
Shankaran, Seetha ;
Walsh, Michele C. ;
Laptook, Abbot R. ;
Newman, Nancy S. ;
Hale, Ellen C. ;
McDonald, Scott A. ;
Das, Abhik ;
Higgins, Rosemary D. .
JOURNAL OF PEDIATRICS, 2013, 162 (06) :1120-+
[6]   Microbes in the neonatal intensive care unit resemble those found in the gut of premature infants [J].
Brooks, Brandon ;
Firek, Brian A. ;
Miller, Christopher S. ;
Sharon, Itai ;
Thomas, Brian C. ;
Baker, Robyn ;
Morowitz, Michael J. ;
Banfield, Jillian F. .
MICROBIOME, 2014, 2
[7]   QIIME allows analysis of high-throughput community sequencing data [J].
Caporaso, J. Gregory ;
Kuczynski, Justin ;
Stombaugh, Jesse ;
Bittinger, Kyle ;
Bushman, Frederic D. ;
Costello, Elizabeth K. ;
Fierer, Noah ;
Pena, Antonio Gonzalez ;
Goodrich, Julia K. ;
Gordon, Jeffrey I. ;
Huttley, Gavin A. ;
Kelley, Scott T. ;
Knights, Dan ;
Koenig, Jeremy E. ;
Ley, Ruth E. ;
Lozupone, Catherine A. ;
McDonald, Daniel ;
Muegge, Brian D. ;
Pirrung, Meg ;
Reeder, Jens ;
Sevinsky, Joel R. ;
Tumbaugh, Peter J. ;
Walters, William A. ;
Widmann, Jeremy ;
Yatsunenko, Tanya ;
Zaneveld, Jesse ;
Knight, Rob .
NATURE METHODS, 2010, 7 (05) :335-336
[8]   Sepsis From the Gut: The Enteric Habitat of Bacteria That Cause Late-Onset Neonatal Bloodstream Infections [J].
Carl, Mike A. ;
Ndao, I. Malick ;
Springman, A. Cody ;
Manning, Shannon D. ;
Johnson, James R. ;
Johnston, Brian D. ;
Burnham, Carey-Ann D. ;
Weinstock, Erica Sodergren ;
Weinstock, George M. ;
Wylie, Todd N. ;
Mitreva, Makedonka ;
Abubucker, Sahar ;
Zhou, Yanjiao ;
Stevens, Harold J. ;
Hall-Moore, Carla ;
Julian, Samuel ;
Shaikh, Nurmohammad ;
Warner, Barbara B. ;
Tarr, Phillip I. .
CLINICAL INFECTIOUS DISEASES, 2014, 58 (09) :1211-1218
[9]   Ribosomal Database Project: data and tools for high throughput rRNA analysis [J].
Cole, James R. ;
Wang, Qiong ;
Fish, Jordan A. ;
Chai, Benli ;
McGarrell, Donna M. ;
Sun, Yanni ;
Brown, C. Titus ;
Porras-Alfaro, Andrea ;
Kuske, Cheryl R. ;
Tiedje, James M. .
NUCLEIC ACIDS RESEARCH, 2014, 42 (D1) :D633-D642
[10]   Mucosa or skin as source of coagulase-negative staphylococcal bacteraemia? [J].
Costa, SF ;
Miceli, MH ;
Anaissie, EJ .
LANCET INFECTIOUS DISEASES, 2004, 4 (05) :278-286