Comparison and assessment of necropsy lesions in end-of-lay laying hens from different housing systems in Denmark.

Apperantly healthy laying hens at the end of production (60 to 91 wk) were investigated for the occurrence of pathology and bacterial infections. In total, 7,477 hens from 15 flocks representing the following production systems: Enriched cages, barn housed layers, and organic/free range layers were necropsied. Indications of bacterial infection were investigated by bacteriological cultivation. The overall prevalence of lesions was 16.60%, including lesions of both infectious and non-infectious origin. The most prevalent lesions were bursitis presternalis (6.65%), reproductive tract lesions (e.g., salpingitis and/or peritonitis and/or oophoritis) (3.50%), serosal scarification (e.g., fibrotic adhesive peritonitis) 1.55%, and neoplasm 1.73%. Significant differences were observed between different production systems and/or flocks in the prevalence of reproductive tract lesions, bursitis presternalis, serosal scarification, skin infections, juvenile hens, and traumas/fractures. No significant difference was observed between different production systems in the prevalence of neoplasia, infection of septicemic etiology, and pododermatitis. In total, 3.4% of the hens were out of lay, with significantly higher rate in organic flocks. Infections of the reproductive tract were the most prevalent lesions with bacterial etiology in all productions systems. In total, 40% of the hens with lesions associated to the oviduct were out of lay and significant difference between production systems were observed. Escherichia coli was the most commonly isolated bacteria and in 90% of the cases they were isolated from the reproductive tract lesions. The second most prevalent bacteria was Gallibacteruim anatis. Significant difference in the prevalence of E. coli positive hens was observed between production systems (P < 0.05). In conclusion, the prevalence of reproductive tract lesions in apparently healthy end-of-lay laying was higher than indicated in previous reports. These findings support the previous suggestions that E. coli and G. anatis are the major pathogens causing reproductive tract lesions.

[1]  John M. Fairbrother,et al.  Colibacillosis , 2019, Diseases of Swine.

[2]  R. Swick,et al.  Performance, egg quality, and liver lipid reserves of free‐range laying hens naturally infected with Ascaridia galli , 2018, Poultry science.

[3]  M. Kogut,et al.  Inflammation: friend or foe for animal production? , 2018, Poultry science.

[4]  J. Christensen,et al.  Longitudinal study of transmission of Escherichia coli from broiler breeders to broilers. , 2017, Veterinary microbiology.

[5]  B. Lupiani,et al.  Marek's disease vaccines: Current status, and strategies for improvement and development of vector vaccines. , 2017, Veterinary microbiology.

[6]  M. Kogut,et al.  Immunometabolic Phenotype Alterations Associated with the Induction of Disease Tolerance and Persistent Asymptomatic Infection of Salmonella in the Chicken Intestine , 2017, Front. Immunol..

[7]  B. Lilje,et al.  Spread of avian pathogenic Escherichia coli ST117 O78:H4 in Nordic broiler production , 2017, BMC Genomics.

[8]  S. Nahashon,et al.  Prevalence and Antimicrobial Resistance of Enterobacteriaceae in Shell Eggs from Small-Scale Poultry Farms and Farmers' Markets. , 2016, Journal of food protection.

[9]  J. Christensen,et al.  Experimental induced avian E. coli salpingitis: Significant impact of strain and host factors on the clinical and pathological outcome. , 2016, Veterinary microbiology.

[10]  J. Christensen,et al.  Pathology and Molecular Characterization of Escherichia Coli Associated With the Avian Salpingitis-Peritonitis Disease Syndrome , 2016, Avian diseases.

[11]  A. Bojesen,et al.  Rapid and accurate identification of Streptococcus equi subspecies by MALDI-TOF MS. , 2015, Systematic and applied microbiology.

[12]  A. Bojesen,et al.  Bacterial determinants of importance in the virulence of Gallibacterium anatis in poultry , 2015, Veterinary Research.

[13]  S. More,et al.  Scientific Opinion on welfare aspects of the use of perches for laying hens , 2015 .

[14]  M. Hess,et al.  Pathogenesis of Gallibacterium anatis in a natural infection model fulfils Koch's postulates: 1. Folliculitis and drop in egg production are the predominant effects in specific pathogen free layers , 2014, Avian pathology : journal of the W.V.P.A.

[15]  J. Christensen,et al.  Variations in virulence of avian pathogenic Escherichia coli demonstrated by the use of a new in vivo infection model. , 2014, Veterinary microbiology.

[16]  H. Hafez,et al.  [Amyloidosis in turkeys (Meleagris gallopavo f. domestica)--a case report]. , 2014, Berliner und Münchener tierärztliche Wochenschrift (1946).

[17]  W. Landman,et al.  Reproduction of the Escherichia coli peritonitis syndrome in laying hens , 2013, Avian Pathology.

[18]  M. Bisgaard,et al.  Causes of Mortality in Commercial Organic Layers in Denmark , 2010, Avian diseases.

[19]  H. Ozaki,et al.  Multiple routes of entry for Escherichia coli causing colibacillosis in commercial layer chickens. , 2009, The Journal of veterinary medical science.

[20]  A. Bojesen,et al.  Tissue distribution of haemolytic Gallibacterium anatis isolates in laying birds with reproductive disorders , 2009, Avian pathology : journal of the W.V.P.A.

[21]  M. Uyttendaele,et al.  Eggshell factors influencing eggshell penetration and whole egg contamination by different bacteria, including Salmonella enteritidis. , 2006, International journal of food microbiology.

[22]  N. Williams,et al.  Observations on salpingitis, peritonitis and salpingoperitonitis in a layer breeder flock , 2005, Veterinary Record.

[23]  T. Johnson,et al.  Comparison of Escherichia coli isolates implicated in human urinary tract infection and avian colibacillosis. , 2005, Microbiology.

[24]  A. Bojesen,et al.  In vivo studies of Gallibacterium anatis infection in chickens , 2004, Avian pathology : journal of the W.V.P.A.

[25]  S. Nielsen,et al.  Prevalence and transmission of haemolytic Gallibacterium species in chicken production systems with different biosecurity levels , 2003, Avian pathology : journal of the W.V.P.A.

[26]  M. Echols Surgery of the avian reproductive tract , 2002 .

[27]  Sherilyn J. Sawyer,et al.  Salpingitis in Pekin Ducks Associated with Concurrent Infection with Tetratrichomonas sp. and Escherichia Coli , 2001, Journal of veterinary diagnostic investigation : official publication of the American Association of Veterinary Laboratory Diagnosticians, Inc.

[28]  W. Landman,et al.  Avian amyloidosis. , 1998, Avian pathology : journal of the W.V.P.A.

[29]  L. N. Payne Leukosis/sarcoma group , 1997 .

[30]  M. Bisgaard Salpingitis in web-footed birds: prevalence, aetiology and significance. , 1995, Avian pathology : journal of the W.V.P.A.

[31]  S. T. Cowan,et al.  Cowan and Steel's manual for the identification of medical bacteria , 1993 .

[32]  T. Fredrickson Ovarian tumors of the hen. , 1987, Environmental health perspectives.

[33]  P. Blackall,et al.  A survey of disease in five commercial flocks of meat breeder chickens. , 1984, Australian veterinary journal.

[34]  M. Bisgaard,et al.  Salpingitis in poultry. II. Prevalence, bacteriology, and possible pathogenesis in egg-laying chickens. , 1981, Nordisk veterinaermedicin.

[35]  P. Klemperer Reticuloendotheliosis. , 2022, Bulletin of the New York Academy of Medicine.