Use of 16S rRNA gene sequencing for prediction of new opportunistic pathogens in chicken ileal and cecal microbiota.

In this study, we addressed differences in the development of gut microbiota in 4 successive batches of commercially hatched broiler parent chickens. When planning this study, we expected to find a batch with compromised performance which would allow identification of microbiota of suboptimal composition. Microbiota composition was determined only by sequencing the V3/V4 region of 16S rRNA genes in samples collected from chickens 5 to 18 wk of age. In a total, 100 and 160 samples originating from the ileum or cecum were processed, respectively. In one of the flocks with suboptimal performance we identified an increased abundance of Helicobacter brantae forming over 80% of ileal microbiota in individual chickens. Moreover, we also tested samples of 53-wk-old hens from the same genetic line in which egg production decreased. In this case, cecal microbiota was enriched for Fusobacterium mortiferum forming over 30% of total cecal microbiota. Although none of the identified unusual microbiota members have been well recognized as pathogenic, they may represent new opportunistic pathogens of chickens worth of further investigation. Analysis of gut microbiota composition by next generation sequencing thus proved as a useful and unbiased alternative to bacterial culture, especially in the cases of unspecific symptoms like decrease in flock performance.

[1]  T. Zhang,et al.  Antibiotic-mediated changes in the fecal microbiome of broiler chickens define the incidence of antibiotic resistance genes , 2018, Microbiome.

[2]  D. Zeng,et al.  Bacillus licheniformis normalize the ileum microbiota of chickens infected with necrotic enteritis , 2018, Scientific Reports.

[3]  P. Lawlor,et al.  Intestinal microbiota profiles associated with low and high residual feed intake in chickens across two geographical locations , 2017, PloS one.

[4]  P. Lawlor,et al.  Fecal Microbiota Transplant from Highly Feed-Efficient Donors Shows Little Effect on Age-Related Changes in Feed-Efficiency-Associated Fecal Microbiota from Chickens , 2017, Applied and Environmental Microbiology.

[5]  Heping Zhang,et al.  Feed-additive probiotics accelerate yet antibiotics delay intestinal microbiota maturation in broiler chicken , 2017, Microbiome.

[6]  J. Weese,et al.  Different antibiotic growth promoters induce specific changes in the cecal microbiota membership of broiler chicken , 2017, PloS one.

[7]  A. Camarinha-Silva,et al.  Insights into Broilers' Gut Microbiota Fed with Phosphorus, Calcium, and Phytase Supplemented Diets , 2016, Front. Microbiol..

[8]  M. Wagner,et al.  Age-Related Differences in the Luminal and Mucosa-Associated Gut Microbiome of Broiler Chickens and Shifts Associated with Campylobacter jejuni Infection , 2016, Front. Cell. Infect. Microbiol..

[9]  J. Volf,et al.  Transient and Prolonged Response of Chicken Cecum Mucosa to Colonization with Different Gut Microbiota , 2016, PloS one.

[10]  T. Kubasová,et al.  Composition of Gut Microbiota Influences Resistance of Newly Hatched Chickens to Salmonella Enteritidis Infection , 2016, Front. Microbiol..

[11]  E. Kiarie,et al.  Impact of combined β-glucanase and xylanase enzymes on growth performance, nutrients utilization and gut microbiota in broiler chickens fed corn or wheat-based diets. , 2016, Poultry science.

[12]  G. Tannock,et al.  Bacterial Succession in the Broiler Gastrointestinal Tract , 2016, Applied and Environmental Microbiology.

[13]  Z. Huang,et al.  Effect of Bacillus subtilis CGMCC 1.1086 on the growth performance and intestinal microbiota of broilers , 2016, Journal of applied microbiology.

[14]  Ondřej Polanský,et al.  Important Metabolic Pathways and Biological Processes Expressed by Chicken Cecal Microbiota , 2015, Applied and Environmental Microbiology.

[15]  Karel Sedlar,et al.  Succession and Replacement of Bacterial Populations in the Caecum of Egg Laying Hens over Their Whole Life , 2014, PloS one.

[16]  Karel Sedlar,et al.  Characterization of Egg Laying Hen and Broiler Fecal Microbiota in Poultry Farms in Croatia, Czech Republic, Hungary and Slovenia , 2014, PloS one.

[17]  C. Constantinidou,et al.  Extensive Microbial and Functional Diversity within the Chicken Cecal Microbiome , 2014, PloS one.

[18]  M. Contreras,et al.  Low Occurrence of Helicobacter DNA in Tropical Wild Birds, Venezuela , 2013, Journal of wildlife diseases.

[19]  F. Haesebrouck,et al.  The local immune response of mice after Helicobacter suis infection: strain differences and distinction with Helicobacter pylori , 2012, Veterinary Research.

[20]  R. Hughes,et al.  Identification and Characterization of Potential Performance-Related Gut Microbiotas in Broiler Chickens across Various Feeding Trials , 2011, Applied and Environmental Microbiology.

[21]  William A. Walters,et al.  QIIME allows analysis of high-throughput community sequencing data , 2010, Nature Methods.

[22]  D. Maes,et al.  Pathogenesis of Helicobacter pullorum infections in broilers. , 2007, International journal of food microbiology.

[23]  F. Dewhirst,et al.  Helicobacter anseris sp. nov. and Helicobacter brantae sp. nov., Isolated from Feces of Resident Canada Geese in the Greater Boston Area , 2006, Applied and Environmental Microbiology.

[24]  S. Tsiodras,et al.  Thyroid Abscess Due to a Mixed Anaerobic Infection with Fusobacterium mortiferum , 2005, Journal of Clinical Microbiology.

[25]  J. Maurer,et al.  Diversity and Succession of the Intestinal Bacterial Community of the Maturing Broiler Chicken , 2003, Applied and Environmental Microbiology.

[26]  T. Horie,et al.  Multibacterial sepsis in an alcohol abuser with hepatic cirrhosis. , 2003, Internal medicine.