BioMed Research International

BioMed Research International / 2013 / Article

Clinical Study | Open Access

Volume 2013 |Article ID 150372 |

A. C. Jenke, J. Postberg, B. Mariel, K. Hensel, D. Foell, J. Däbritz, S. Wirth, "S100A12 and hBD2 Correlate with the Composition of the Fecal Microflora in ELBW Infants and Expansion of E. coli Is Associated with NEC", BioMed Research International, vol. 2013, Article ID 150372, 8 pages, 2013.

S100A12 and hBD2 Correlate with the Composition of the Fecal Microflora in ELBW Infants and Expansion of E. coli Is Associated with NEC

Academic Editor: Hongjuan Liu
Received17 Jul 2013
Revised03 Sep 2013
Accepted09 Sep 2013
Published06 Nov 2013


Objective. To describe the development of the gut microbiota in extremely low birth weight (ELBW) infants with and without necrotizing enterocolitis (NEC) between April 2008 and December 2009, fecal microflora was prospectively analyzed in fecal samples of all ELBW infants using real-time PCR assays. In addition, fecal inflammatory were measured. Results. Fecal microflora established early in ELBW infants and microbiota composition remained stable over the first 28 days of life except for the prevalence of C. difficile which decreased with decreasing antibiotic use. Infants who subsequently developed NEC had an increase of total bacterial count (9.8-fold) 24 h prior to clinical symptoms mainly due to the expansion of E. coli species (21.6-fold), whereas microbiota composition did not differ from healthy ELBW infants five days before onset of NEC. Importantly, S100A12 and hBD2 positively correlated with the total and E. coli bacterial CFU/g feces ( 0.4 and 0.64, resp.). Conclusions. In summary, we found evidence for a disturbed homeostasis between the intestinal microbiome and host immunity in ELBW infants with NEC. Moreover, S100A12 and hBD2 correlate with the fecal microbiota thus linking the intestinal innate immune response to the bacterial colonization thus possibly providing a diagnostic tool in the future.

1. Introduction

Necrotizing enterocolitis (NEC) is a devastating disease affecting primarily premature infants. Although its etiology still remains unclear, the most widely accepted hypothesis is that NEC develops in the stressed, premature host suffering from an immature innate and adaptive immune system (reviewed in [1]) after a disruption in the intestinal barrier and translocation of bacterial endotoxins [2, 3]. Previous studies have shown that gut colonization in preterm infants is often delayed [4] and shows decreased diversity and abnormal microbiota, particularly in patients who develop NEC [58]. In addition, NEC has not been observed in germ-free animals [9] and infants with NEC frequently exhibit concomitant bacteremia and endotoxemia [10]. Although bacterial colonization in premature infants seems to be influenced by many host and environmental factors (reviewed in [8]), data on these processes is limited in extremely low birth weight (ELBW) infants who carry the highest risk for NEC with insufficient clinical data linking fecal inflammatory markers and antimicrobial peptides to fecal microbiota. This is particularly the case for S100A12, an endogenous damage-associated molecular pattern molecule released by activated or damaged cells under conditions of cell stress [11], and hBD2, an antimicrobial peptide and important factor in the innate host defense at the mucosal surface of the gastrointestinal tract [12]. We have previously analyzed these fecal biomarkers in ELBW infants demonstrating (i) that fecal calprotectin (fCP) levels depend on gestational and postnatal age and have a lower limit [13], (ii) that fecal S100A12 has an improved sensitivity and specificity for the detection of NEC when compared to fCP [14], and (iii) that high fecal and intestinal hBD2 concentrations, reflecting a strong intestinal immune response, were associated with a moderate course of NEC in ELBW infants [15].

Here, we now describe the development of the intestinal microbiota in ELBW infants with and without NEC. Importantly, in contrast to previous studies, we prospectively monitored the fecal inflammatory biomarkers fCP, S100A12, and hBD2 and correlated these with the composition of the intestinal microbiota in fecal samples of ELBW infants. By this means, we provide new insights into the development of intestinal microbiota in ELBW infants and their interaction with the intestinal innate immune system.

2. Material and Methods

2.1. Patient Cohort and Sample Collection

The same cohort of extremely low birth weight infants (gestational age up to 27 + 0 weeks, born <1000 g) was used as described previously [15]. Gestational age (GA) was determined based on fetal ultrasound before the 14th week of gestation. Stool samples were prospectively collected on alternate days for the first four weeks of life. Immediately after collection samples were stored for a maximum of 48 h at 4°C and then stored at −80°C. In addition, epidemiological parameters and data about the hospital course were collected daily. NEC was defined as NEC ≥ stage 2a according to the modified Bell’s criteria. Patients with spontaneous intestinal perforation (SIP) were excluded from the study.

2.2. Calprotectin, hBD2, and S100A12 Analysis in Fecal Samples

Fecal calprotectin (Immundiagnostik, Bensheim, Germany) and hBD2 (Immundiagnostik, Bensheim, Germany) concentrations were determined by enzyme-linked immunosorbent assays (ELISA) [16, 17] and S100A12 concentrations by double-sandwich ELISA as described previously [18]. All analyses were performed in triplicate and normalized against controls provided by the manufacturers or the in-house S100A12 standards, respectively. Intra- and interassay coefficients of variation were <5% and <15%, respectively. Laboratory personnel were blinded to the origin and identity of patient samples.

2.3. DNA Purification from Feces and Microbial Analysis with Real-Time PCR Assays

Fecal samples were 10-fold diluted in peptone/water. Bacterial DNA was isolated using the QIAamp DNA stool mini kit (Qiagen, Hilden, Germany) according to the instructions provided by the manufacturer. DNA was eluted in a final volume of 200 µL. DNA from all fecal samples was subjected to real-time PCR assays for Bifidobacteria, E. coli, C. difficile, Bacteroides fragilis group, Lactobacilli, and total bacteria based on 16S rDNA gene sequences as described previously [19]. In all cases, the SYBR Green I method (Bio-Rad Laboratories, Hercules, CA, USA) was used: Bifido_fw 5′-gcgtgcttaacacatgcaagtc-3′Bifido_rv 5′-cacccgtttccaggagctatt-3′E_coli_fw 5′-catgccgcgtgtatgaagaa-3′E_coli_rv 5′-cgggtaacgtcaatgagcaaa-3′C_difficile_fw 5′-ttgagcgatttacttcggtaaaga-3′C_difficile_rv 5′-tgtactggctcacctttgatattca-3′B_fragilis_fw 5′-cggaggatccgagcgtta-3′B_fragilis_rv 5′-ccgcaaactttcacaactgactta-3′Bifidobact_inf_fw 5′-ccccgtgttgccagcggatt-3′Lactobac spp for 5′-agcagtagggaatcttcca-3′Lactobac spp rev 5′-caccgctacacatggag-3′Total count for 5′-tcctacgggaggcagcagt-3′Total count rev 5′-ggactaccagggtatctaatcctgtt-3′

PCR conditions were as follows: 95°C for 15 min, 40 cycles of (95°C for 15 seconds and 60°C for 30 seconds). Melting of PCR product was performed using a temperature gradient from 55°C to 95°C, rising in 0.5°C increments.

2.4. Statistical Analysis

Median quantification levels of all analyzed microbes were obtained from triplicate real-time PCR measurements. Data are presented as the median +/− interquartile range (IQR), minimum, and maximum. Testing for significant differences between groups was performed using the one-way ANOVA test for values with Gaussian distribution and the Mann-Whitney test for values without Gaussian distribution. The Kolmogorov-Smirnov test was utilized to rule out non-Gaussian distribution. Values for were considered statistically significant. All analyses were performed using GraphPad version 5.01 (La Jolla, CA USA).

3. Results

3.1. Epidemiological Characteristics

68 ELBW infants were included in this study. Among those, 12 subsequently developed NEC and 56 had no gastrointestinal disorders (Table 1). We observed no significant differences between the disease and control group except for that infants who subsequently developed NEC tended to have a higher prevalence for antibiotic therapy at day 7 of life (Table 1). Six patients with NEC required surgery, whilst none in the other group. Mortality rate of NEC was 33% ( ), whereas in the other group no patients died. A total of 248 fecal samples were analyzed: 59 at the postnatal age of 7 days, 64 at 14 days, 59 at 21 days, and 50 at 28 days (mean 3.4 per individual, range 2 to 4) and 16 additional samples in patients with NEC in association with the disease.

Group with NEC stage ≥2 ( )Control group without any GI problems ( )P value

Gestational age25.4 (24.2–27)25.3 (23.3–27)ns
Birth weight in g747 (650–890)751 (354–990)ns
Umbilical artery pH at birth7.34 (7.26–7.45)7.32 (7.23–7.45)ns
CrP at birth in mg/dL1.52 (0.3–4.32)1.67 (0.2–4.64)ns
Oral feeding day 7 in mL/kg92.4 (50–142)84.9 (50–168)ns
Parenteral fluids day 7 in mL/kg77.6 (21–140)78.8 (0–128)ns
Mean onset of NEC (postnatal day)14.8 (8–28)
Female (N)50% (6)58.9% (33)ns
Delivery per caesarean section (N)91.6% (11)91.1% (51)ns
Antibiotic therapy at day 7 (N)83.3% (10)66% (37)ns
Exclusively breast fed at day 7 (N)16.7% (2)19.6% (11)ns
MEDIAN LOG10 CFU per mg at day 7
 Total Bacterial count8.5 (8.2–10.7)8.7 (7.8–9.1)ns
Lactobacilli 8.1 (7.2–9.0)7.4 (6.9–8.2)<0.01
C. difficile (if positive)7.5 (4.8–11.0)5.9 (5.2–9.6)ns
E. coli 7.0 (6.0–7.6)7.5 (6.6–7.9)<0.05
Bifidobacteria 7.4 (6.1–7.7)7.6 (5.5–7.9)ns
B. fragilis group 6.0 (5.2–6.6)6.0 (5.4–6.7)ns
 Others 7.7 (7.2–10.2)7.9 (6.8–10.9)ns
Prevalence of C. difficile at day 7 (N)33.3% (4)26.8% (15)ns

3.2. The Intestinal Microflora in ELBW Infants Is Established during the First Week of Life, While the Use of Antibiotics Influences C. difficile Prevalence

At the age of 7 days, there were no significant differences in the median total CFU/g feces between infants who subsequently developed NEC and healthy ELBW infants except for a higher proportion of Lactobacilli and a lower proportion of E. coli in the NEC group. Also, the prevalence of C. difficile was slightly higher in the NEC group (Table 1). Bifidobacteria, E. coli, Bacteroides fragilis group, and Lactobacilli were detectable in all patients and in more than 98% of the samples. When further investigating factors associated with the prevalence of C. difficile, we did not find any influence of a specific hospital or mode of delivery, but antibiotic therapy for more than 48 h during the first week of life was associated with a higher prevalence of C. difficile at the age of 7 postnatal days (23 versus 35%, OR 1.78 (0.94–3.38), ). At this age, the prevalence of antibiotic therapy in healthy ELBW infants was 66% and 83% in infants who subsequently developed NEC. In healthy ELBW infants, the prevalence of antibiotic therapy slowly declined thereafter to 53% at day 14 and 31% at days 21 and 28 which was mirrored by a similar decline in C. difficile prevalence from 33% to 25% and 19% at days 7, 14, and 28, respectively. Otherwise the overall relative composition of the fecal microflora in the reference population remained stable during the first four weeks of life (Figure 1).

3.3. The Composition of the Fecal Microbiota Is Altered in Patients with NEC Shortly before Onset of Symptoms

Next, we analyzed the dynamics of the composition of the fecal microbiota in infants who subsequently developed NEC. Here, we noted a marked 9.8-fold increase in the median total bacterial count shortly before onset of clinical symptoms when compared to a previous time point both in the same patients and the reference population (Figure 2(a)). This expansion was paralleled by a substantial change in the composition of the fecal microbiota mainly characterized by a steep increase in the median E. coli CFU/g by 21.6-fold (Table 2) and a trend for a lower median percentage of other bacteria not detected by our RT-PCR assays shortly before NEC (11.9% (9.1–19.9, range 2.2 to 24.1)) when compared to a period 90 to 120 h before onset of clinical symptoms (16.7% (12.3–24.2, range 9.6 to 37.9); ). However, on an individual level, two of the twelve patients (16.7%) also showed a substantial decrease in total bacterial and E. coli CFU/g feces before NEC (Figures 2(b)–2(d)).

96 to 120 h prior to NEC ( )Within 24 h of onset of NEC ( )P value

MEDIAN LOG10 CFU per g at day 7
 Total bacterial count9 (8.4–10.4)9.9 (9.4–10.6)0.04
Lactobacilli 8.7 (7.8–10.5)8.9 (8.6–9.2)0.49
C. difficile (if positive)6.3 (4.4–8.3)6.7 (4.1–9.3)0.46
E. coli 7.9 (5.1–8.1)9.5 (8.8–10.3)<0.001
Bifidobacteria 7.5 (5.1–7.6)8.3 (6.7–9.2)0.11
B. fragilis group 5.8 (5.6–6.3)7.0 (6.6–7.3)0.28
 Others8.6 (7.7–9.9)9.1 (8.4–9.5)0.44
Prevalence of C. difficile (N)33.3% (4)27.2% (3)

3.4. S100A12 and hBD2 Directly Correlate with Total and E. coli CFU/g Feces

In the last part of this study, we correlated fecal antimicrobial peptides and inflammatory markers with fecal microbiota. Here, we did not find any correlation between fCP levels and total bacterial count or any of the analyzed bacteria (Figures 3(a) and 3(b)). In contrast even though S100A12 did not correlate with CFU/g feces of Lactobacilli, Bifidobacteria or B. fragilis group, it directly correlated with the total bacterial and E. coli count with a correlation coefficient of 0.4 in both cases (Figures 3(c) and 3(d)). Interestingly, the antimicrobial peptide hBD2 showed a similar direct correlation with total bacterial and E. coli count with of 0.69 and 0.64, respectively (Figures 3(e) and 3(f)). A combination of hBD2 and S100A12 did not improve the correlation coefficient or predictive value compared to the use as single parameters.

4. Discussion

It is clear that intestinal microbiota have a role in the pathogenesis of necrotizing enterocolitis (NEC) and it is undoubted that a better understanding of the physiology of bacterial colonization in premature infants under per se nonphysiological conditions of a neonatal intensive care unit is an important tessera to elucidate mechanisms predisposing these infants to NEC. Since several previous studies revealed contradicting results, more data is needed to better characterize the exact role of intestinal microbiota in NEC pathogenesis.

In this study, we investigate the development of the intestinal microbiota in a large cohort of ELBW infants including 12 cases of NEC. Even though we did not sequence 16S bacterial rRNA subunits but used real-time PCR assays instead, we included all major groups of intestinal bacteria like Actinobacteria (Bifidobacteria), Firmicutes (Lactobacilli and C. difficile), Proteobacteria (E. coli), and Bacteroides (Bacteroides fragilis group) [19]. Moreover, this is the first study to our knowledge that in parallel measured the fecal inflammatory markers calprotectin (fCP) and S100A12 and the antimicrobial peptide hBD2 and correlated these with fecal microbiota.

Interestingly, in contrast to several previous studies [20, 21], we found Lactobacilli, Bifidobacteria, E. coli, and B. fragilis group in all patients after the first week of life. Particularly surprising was this observation for B. fragilis group since the rate of cesarean section was above 90% in our study group and colonization with B. fragilis group has been previously reported to depend on the mode of delivery with much lower prevalence in infants born through cesarean section [22]. Since patients in our study were included at several separated NICUs, this cannot be biased by a site-associated effect. To date, we therefore can only speculate that differences in analytical techniques and in study populations may account for this observation. The prevalence of C. difficile was within limits of previous reports [1921]. We also found a direct correlation between the prevalence of antibiotic therapy and C. difficile colonization as described previously [19]. Regarding the further development of the intestinal microbiome, we found only minor variations during the following weeks in spite of increasing amounts of enteral and decreasing of parenteral feeding. The only exception was a decrease in the prevalence of C. difficile paralleled by a reduced frequency of antibiotic therapy. It therefore seems that the primary colonization has a long impact on the intestinal microbiota which is in line with previous studies on mouse models [23]. When comparing the early fecal microbiota of premature infants without gastrointestinal disorders with infants who subsequently developed NEC, we did not find significant differences but observed a tendency to higher medium CFU/g feces of C. difficile. However, regarding the development of NEC, we noted a rapid substantial increase in the median total bacterial CFU/g feces which mainly consisted of an increase in the median number of E. coli. This is in line with a previous report suggesting that premature infants might develop NEC possibly due to the insufficiency to mount an adequate adaptive immunological response to a subsequent expansion of Proteobacteria later in life [7]. This idea is also supported by recent data from a mouse model showing that gram-negative bacteria are associated with early stages of NEC when inflammatory markers are still negative [24]. Similarly, a high susceptibility of the premature porcine gut to E. coli infection has been demonstrated after delivery through cesarean section and in the absence of breastfeeding [25].

Furthermore, we found that the antimicrobial peptide hBD2 directly correlated with the total bacterial and E. coli CFU/g feces. Since hBD2 is at least partly regulated by TLR4 and MD2 signaling [26, 27], which is mainly stimulated by lipopolysaccharide (LPS), the glycolipid component of the outer membrane of gram-negative bacteria such as E. coli, this finding links the microbiota to the intestinal innate immunity. Importantly, we have reported earlier that ELBW infants with a particularly severe course of NEC lack an increase in hBD2 [15]. This adds further evidence to the hypothesis that an inadequate intestinal innate immune response to the intestinal microbiota plays an important role in the development of NEC. Nevertheless, we would like to emphasize that there were also patients without an increase and even a decrease in total bacterial and E. coli CFU/g feces prior to NEC and there was a considerable individual variation in bacterial composition as described previously [28]. Therefore, we believe that the observed changes in fecal microbiota do not represent a sine qua non condition for the development of NEC and are more likely just a symptom of a disturbed homeostasis at the intestinal endothelial barrier. In addition, it is important to keep in mind that fecal microbiota may not necessarily represent microbiota at the point of intestinal injury [29, 30].

Regarding the analysis of inflammatory markers, we found no correlation between fCP and fecal microbiota which is in line with a previous report [31]. Neutrophil-derived S100A12 in contrast correlated, similar to hBD2, with total bacterial and E. coli count possibly explaining why S100A12 is more sensitive and specific in predicting NEC than fCP [14].

In summary, this study provides additional evidence for the role of a differential intestinal colonization in NEC pathogenesis. Moreover, we show that the hBD2 and S100A12 directly correlate with the composition of the fecal microbiota linking it to the intestinal innate immunity. Further studies analyzing this complex interaction between gut microbes and the intestinal innate immune system might be a promising approach to gain new insights into the pathophysiology and etiology of NEC.

Ethical Approval

This study was conducted with approval of the Witten/Herdecke University Ethics Board.

Conflict of Interests

None of the authors had any conflict of interests.


This study was funded by the HELIOS Research Center (HRC). D. Foell and J. Däbritz received funding from the German Research Foundation (DFG FO354/3-1 and DFG DA1161/4-1). The authors would like to thank Claudia Förster for her excellent technical support.


  1. J. Neu and W. A. Walker, “Necrotizing enterocolitis,” The New England Journal of Medicine, vol. 364, no. 3, pp. 255–264, 2011. View at: Publisher Site | Google Scholar
  2. C. L. Leaphart, F. Qureshi, S. Cetin et al., “Interferon-γ Inhibits Intestinal Restitution by Preventing Gap Junction Communication Between Enterocytes,” Gastroenterology, vol. 132, no. 7, pp. 2395–2411, 2007. View at: Publisher Site | Google Scholar
  3. R. Sharma, J. J. Tepas III, M. L. Hudak et al., “Neonatal gut barrier and multiple organ failure: role of endotoxin and proinflammatory cytokines in sepsis and necrotizing enterocolitis,” Journal of Pediatric Surgery, vol. 42, no. 3, pp. 454–461, 2007. View at: Publisher Site | Google Scholar
  4. J. L. Blakey, L. Lubitz, and G. L. Barnes, “Development of gut colonisation in pre-term neonates,” Journal of Medical Microbiology, vol. 15, no. 4, pp. 519–529, 1982. View at: Google Scholar
  5. Y. Wang, J. D. Hoenig, K. J. Malin et al., “16S rRNA gene-based analysis of fecal microbiota from preterm infants with and without necrotizing enterocolitis,” ISME Journal, vol. 3, no. 8, pp. 944–954, 2009. View at: Publisher Site | Google Scholar
  6. M. Mshvildadze, J. Neu, J. Shuster, D. Theriaque, N. Li, and V. Mai, “Intestinal microbial ecology in premature infants assessed with non-culture-based techniques,” Journal of Pediatrics, vol. 156, no. 1, pp. 20–25, 2010. View at: Publisher Site | Google Scholar
  7. V. Mai, C. M. Young, M. Ukhanova et al., “Fecal microbiota in premature infants prior to necrotizing enterocolitis,” PLoS One, vol. 6, no. 6, Article ID e20647, 2011. View at: Publisher Site | Google Scholar
  8. M. S. Cilieborg, M. Boye, and P. T. Sangild, “Bacterial colonization and gut development in preterm neonates,” Early Human Development, vol. 88, supplement 1, pp. S41–S49, 2012. View at: Publisher Site | Google Scholar
  9. M. J. Morowitz, V. Poroyko, M. Caplan, J. Alverdy, and D. C. Liu, “Redefining the role of intestinal microbes in the pathogenesis of necrotizing enterocolitis,” Pediatrics, vol. 125, no. 4, pp. 777–785, 2010. View at: Publisher Site | Google Scholar
  10. A. Schwiertz, B. Gruhl, M. Löbnitz, P. Michel, M. Radke, and M. Blaut, “Development of the intestinal bacterial composition in hospitalized preterm infants in comparison with breast-fed, full-term infants,” Pediatric Research, vol. 54, no. 3, pp. 393–399, 2003. View at: Publisher Site | Google Scholar
  11. D. Foell, H. Wittkowski, Z. Ren et al., “Phagocyte-specific S100 proteins are released from affected mucosa and promote immune responses during inflammatory bowel disease,” Journal of Pathology, vol. 216, no. 2, pp. 183–192, 2008. View at: Publisher Site | Google Scholar
  12. K. M. Huttner and C. L. Bevins, “Antimicrobial peptides as mediators of epithelial host defense,” Pediatric Research, vol. 45, no. 6, pp. 785–794, 1999. View at: Google Scholar
  13. L. Zoppelli, C. Guttel, H. J. Bittrich, C. Andree, S. Wirth, and A. Jenke, “Fecal calprotectin concentrations in premature infants have a lower limit and show postnatal and gestational age dependence,” Neonatology, vol. 102, no. 1, pp. 68–74, 2012. View at: Publisher Site | Google Scholar
  14. J. Dabritz, A. Jenke, S. Wirth, and D. Foell, “Fecal phagocyte-specific S100A12 for diagnosing necrotizing enterocolitis.,” Journal of Pediatrics, vol. 161, no. 6, pp. 1059–1064, 2012. View at: Publisher Site | Google Scholar
  15. A. C. Jenke, M. Zilbauer, J. Postberg, and S. Wirth, “Human beta-defensin 2 expression in ELBW infants with severe necrotizing enterocolitis.,” Pediatric Research, vol. 72, no. 5, pp. 513–520, 2012. View at: Publisher Site | Google Scholar
  16. M. Richter, H.-G. Topf, M. Gröschl et al., “Influence of gestational age, cesarean section, and type of feeding on fecal human β-defensin 2 and tumor necrosis factor-α,” Journal of Pediatric Gastroenterology and Nutrition, vol. 51, no. 1, pp. 103–105, 2010. View at: Publisher Site | Google Scholar
  17. O. Schröder, M. Naumann, Y. Shastri, N. Povse, and J. Stein, “Prospective evaluation of faecal neutrophil-derived proteins in identifying intestinal inflammation: combination of parameters does not improve diagnostic accuracy of calprotectin,” Alimentary Pharmacology and Therapeutics, vol. 26, no. 7, pp. 1035–1042, 2007. View at: Publisher Site | Google Scholar
  18. D. Foell, T. Kucharzik, M. Kraft et al., “Neutrophil derived human S100A12 (EN-RAGE) is strongly expressed during chronic active inflammatory bowel disease,” Gut, vol. 52, no. 6, pp. 847–853, 2003. View at: Publisher Site | Google Scholar
  19. J. Penders, C. Thijs, C. Vink et al., “Factors influencing the composition of the intestinal microbiota in early infancy,” Pediatrics, vol. 118, no. 2, pp. 511–521, 2006. View at: Publisher Site | Google Scholar
  20. H. Sakata, H. Yoshioka, and K. Fujita, “Development of the intestinal flora in very low birth weight infants compared to normal full-term newborns,” European Journal of Pediatrics, vol. 144, no. 2, pp. 186–190, 1985. View at: Google Scholar
  21. P. L. Stark and A. Lee, “The bacterial colonization of the large bowel of pre-term low birth weight neonates,” Journal of Hygiene, vol. 89, no. 1, pp. 59–67, 1982. View at: Google Scholar
  22. M.-M. Grönlund, O.-P. Lehtonen, E. Eerola, and P. Kero, “Fecal microflora in healthy infants born by different methods of delivery: permanent changes in intestinal flora after cesarean delivery,” Journal of Pediatric Gastroenterology and Nutrition, vol. 28, no. 1, pp. 19–25, 1999. View at: Publisher Site | Google Scholar
  23. T. Olszak, D. An, S. Zeissig et al., “Microbial exposure during early life has persistent effects on natural killer T cell function,” Science, vol. 336, no. 6080, pp. 489–493, 2012. View at: Publisher Site | Google Scholar
  24. E. M. Carlisle, V. Poroyko, M. S. Caplan, J. A. Alverdy, and D. Liu, “Gram negative bacteria are associated with the early stages of necrotizing enterocolitis,” PLoS One, vol. 6, no. 3, Article ID e18084, 2011. View at: Publisher Site | Google Scholar
  25. M. L. Jensen, M. S. Cilieborg, M. V. Ostergaard, S. B. Bering, C. B. Jorgensen, and P. T. Sangild, “Escherichia coli challenge in newborn pigs,” Journal of Animal Science, vol. 90, supplement 4, pp. 43–45, 2012. View at: Google Scholar
  26. D. Varoga, E. Klostermeier, F. Paulsen et al., “The antimicrobial peptide HBD-2 and the Toll-like receptors-2 and -4 are induced in synovial membranes in case of septic arthritis,” Virchows Archiv, vol. 454, no. 6, pp. 685–694, 2009. View at: Publisher Site | Google Scholar
  27. S. Gariboldi, M. Palazzo, L. Zanobbio et al., “Low molecular weight hyaluronic acid increases the self-defense of skin epithelium by induction of β-defensin 2 via TLR2 and TLR4,” Journal of Immunology, vol. 181, no. 3, pp. 2103–2110, 2008. View at: Google Scholar
  28. F. Magne, A. Suau, P. Pochart, and J.-F. Desjeux, “Fecal microbial community in preterm infants,” Journal of Pediatric Gastroenterology and Nutrition, vol. 41, no. 4, pp. 386–392, 2005. View at: Publisher Site | Google Scholar
  29. P. B. Eckburg, E. M. Bik, C. N. Bernstein et al., “Microbiology: diversity of the human intestinal microbial flora,” Science, vol. 308, no. 5728, pp. 1635–1638, 2005. View at: Publisher Site | Google Scholar
  30. P. Lepage, P. Seksik, M. Sutren et al., “Biodiversity of the mucosa-associated microbiota is stable along the distal digestive tract in healthy individuals and patients with IBD,” Inflammatory Bowel Diseases, vol. 11, no. 5, pp. 473–480, 2005. View at: Publisher Site | Google Scholar
  31. M. V. Björkström, L. Hall, S. Söderlund, E. G. Håkansson, S. Håkansson, and M. Domellöf, “Intestinal flora in very low-birth weight infants,” Acta Paediatrica, International Journal of Paediatrics, vol. 98, no. 11, pp. 1762–1767, 2009. View at: Publisher Site | Google Scholar

Copyright © 2013 A. C. Jenke et al. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

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