Original Articles

Detection of Chlamydia ibidis in the neck skin microbiome of broiler carcasses at the end of slaughter

Publisher's note
All claims expressed in this article are solely those of the authors and do not necessarily represent those of their affiliated organizations, or those of the publisher, the editors and the reviewers. Any product that may be evaluated in this article or claim that may be made by its manufacturer is not guaranteed or endorsed by the publisher.
Received: 12 December 2025
Published: 4 March 2026
146
Views
113
Downloads

Authors

Chlamydia is the etiological agent of chlamydiosis in wild and domestic birds, mammals, and humans. In this study, Chlamydia reads were detected in the microbiome of the neck skin of 76 broiler carcasses collected in the same slaughterhouse at the end of the chilling tunnel. The carcasses originated from four different flocks of female Ross 308, reared in two broiler houses located in Northern Italy. One flock from each poultry house was sampled in 2019 and one flock in 2023. The carcass neck skin microbiome was investigated by shotgun metagenomic sequencing. Chlamydia reads displayed a mean relative abundance of 7.38%, with significant differences between carcasses obtained from the two poultry houses, sampled at both sampling times. Chlamydia ibidis was the prevalent species among time points and poultry houses. The zoonotic potential of C. ibidis and foodborne transmission have never been demonstrated. However, it is known that the genus Chlamydia has “spore”-like extracellular forms able to survive for months outside the host. Therefore, the presence of C. ibidis reads on broiler carcasses at the end of the chilling tunnel deserves further investigation. The results of this study highlight the feasibility of microbiome investigations to detect unexpected biological hazards in foods. 

Downloads

Download data is not yet available.

Commission of the European Communities, 2005. Commission Regulation (EC) No. 2073/2005 of the European Parliament and of the Council of 15 November 2005 on microbiological criteria for foodstuffs. In: Official Journal, L338/1, 22/12/2005.

De Cesare A, Caselli E, Lucchi A, Sala C, Parisi A, Manfreda G, Mazzacane S, 2019. Impact of a probiotic-based cleaning product on the microbiological profile of broiler litters and chicken cae-ca microbiota. Poult Sci 98:3602-10. DOI: https://doi.org/10.3382/ps/pez148

De Meyst A, De Clercq P, Porrez J, Geens T, Braeckman L, Ouburg S, Morré SA, Vanrompay D, 2024. Belgian cross-sectional epidemiological study on zoonotic avian Chlamydia spp. in chick-ens. Microorganisms 12:193. DOI: https://doi.org/10.3390/microorganisms12010193

Dembek ZF, Mothershead JL, Owens AN, Chekol T, Wu A, 2023. Psittacosis: an underappreciated and often undiagnosed disease. Pathogens 12:1165. DOI: https://doi.org/10.3390/pathogens12091165

EFSA, 2024. The European Union One Health 2023 zoonoses report, 2024. EFSA J 22:e9016. DOI: https://doi.org/10.2903/j.efsa.2024.p221202

EFSA Panel on Biological Hazards (BIOHAZ), Koutsoumanis K, Allende A, Álvarez-Ordóñez A, Bolton D, Bover-Cid S, Chemaly M, Davies R, De Cesare A, Herman L, Hilbert F, Lindqvist R, Nauta M, Ru G, Simmons M, Skandamis P, Suffredini E, Argüello H, Berendonk T, Cavaco LM, Gaze W, Schmitt H, Topp E, Guerra B, Liébana E, Stella P, Peixe L, 2021. Role played by the environment in the emergence and spread of antimicrobial resistance (AMR) through the food chain. EFSA J 19:e06651. DOI: https://doi.org/10.2903/j.efsa.2021.6651

EFSA Panel on Biological Hazards (BIOHAZ), Koutsoumanis K, Allende A, Álvarez-Ordóñez A, Bolton D, Bover-Cid S, Chemaly M, Davies R, De Cesare A, Herman L, Hilbert F, Lindqvist R, Nauta M, Ru G, Simmons M, Skandamis P, Suffredini E, Argüello-Rodríguez H, Dohmen W, Magistrali CF, Padalino B, Tenhagen B-A, Threlfall J, García-Fierro R, Guerra B, Liébana E, Stella P, Peixe L, 2022. Transmission of antimicrobial resistance (AMR) during animal transport. EFSA J 20:e07586. DOI: https://doi.org/10.2903/j.efsa.2022.7586

Essig A, Longbottom D, 2015. Chlamydia abortus: new aspects of infectious abortion in sheep and potential risk for pregnant women. Curr Clin Microbiol Rep 2:22-34. DOI: https://doi.org/10.1007/s40588-015-0014-2

European Parliament, Council of the European Union, 2002. Commission Regulation (EC) No 178/2002 of the European Parliarment and of the Council of 28 January 2002 laying down the general principles and requirements of food law, establishing the European Food Safety Authori-ty and laying down proc dures in matters of food safety. In: Official Journal, L 031, 28/01/2002.

Heijne M, Jelocnik M, Umanets A, Brouwer MSM, Dinkla A, Harders F, van Keulen LJM, Roest HJ, Schaafsma F, Velkers FC, van der Goot JA, Pannekoek Y, Koets AP, 2021. Genetic and phenotypic analysis of the pathogenic potential of two novel Chlamydia gallinacea strains com-pared to Chlamydia psittaci. Sci Rep 11:16516. DOI: https://doi.org/10.1038/s41598-021-95966-9

Hogerwerf L, Holstege MMC, Benincà E, Dijkstra F, van der Hoek W, 2017. Temporal and spatial analysis of psittacosis in association with poultry farming in the Netherlands, 2000-2015. BMC Infect Dis 2017;17:519. DOI: https://doi.org/10.1186/s12879-017-2608-1

Kaleta EF, Taday EMA, 2003. Avian host range of Chlamydophila spp. based on isolation, antigen detection and serology. Avian Pathol 32:435-61. DOI: https://doi.org/10.1080/03079450310001593613

Kowalczyk K, Wójcik-Fatla A, 2022. Chlamydia psittaci in faecal samples of feral pigeons (Columba livia forma urbana) in urban areas of Lublin city, Poland. Curr Microbiol 79:367. DOI: https://doi.org/10.1007/s00284-022-03072-4

Krawiec M, Piasecki T, Wieliczko A, 2015. Prevalence of Chlamydia psittaci and Other Chlamydia Species in Wild Birds in Poland. Vector Borne Zoonotic Dis 15:652-55. DOI: https://doi.org/10.1089/vbz.2015.1814

Laroucau K, Aaziz R, Meurice L, Servas V, Chossat I, Royer H, de Barbeyrac B, Vaillant V, Moyen JL, Meziani F, Sachse K, Rolland P, 2015. Outbreak of psittacosis in a group of women exposed to Chlamydia psittaci-infected chickens. Euro Surveill 20:21155. DOI: https://doi.org/10.2807/1560-7917.ES2015.20.24.21155

Lee HJ, Lee OM, Kang SI, Yeo YG, Jeong JY, Kwon YK, Kang MS, 2023. Prevalence of asympto-matic infections of Chlamydia psittaci in psittacine birds in Korea. Zoonoses Public Health 70:451-8. DOI: https://doi.org/10.1111/zph.13039

Long J-M, Zhong H-T, Deng Y-Y, Yang J-W, Chen M-C, Liang Y-J, Chen K-W, Yang J-T, Wei T-C, Wei P, Huang J-N, 2025. Prevalence and genetic characteristics of avian Chlamydia in birds in Guangxi, Southwestern China. Microorganisms 13:2220. DOI: https://doi.org/10.3390/microorganisms13092220

Marchino M, Rizzo F, Barzanti P, Sparasci OA, Bottino P, Vicari N, Rigamonti S, Braghin S, Aaziz R, Vorimore F, Ru G, Laroucau K, Mandola ML, 2022. Chlamydia species and related risk fac-tors in poultry in North-Western Italy: possible bird-to-human transmission for C. gallinacea. Int J Environ Res Public Health 19:2174. DOI: https://doi.org/10.3390/ijerph19042174

Marmion M, Ferone MT, Whyte P, Scannell AGM, 2021. The changing microbiome of poultry meat; from farm to fridge. Food Microbiol 99:103823. DOI: https://doi.org/10.1016/j.fm.2021.103823

Menzel P, Ng KL, Krogh A, 2016. Fast and sensitive taxonomic classification for metagenomics with Kaiju. Nat Commun 7:11257. DOI: https://doi.org/10.1038/ncomms11257

Ossa-Giraldo AC, Úsuga-Perilla X, Correa JS, Segura JA, 2023. Chlamydia psittaci seropositivity in workers exposed to birds and review of the literature: Evidence of circulation in Antioquia. Bio-medica 43:330-43. DOI: https://doi.org/10.7705/biomedica.6832

Park J, Bae D, Kim SA, 2023. Microbial trace investigation throughout the entire chicken supply chain based on metagenomic high-throughput sequencing. Food Res Int 169:112775. DOI: https://doi.org/10.1016/j.foodres.2023.112775

Rehn M, Ringberg H, Runehagen A, Herrmann B, Olsen B, Petersson AC, Hjertqvist M, Kühlmann-Berenzon S, Wallensten A, 2013. Unusual increase of psittacosis in southern Sweden linked to wild bird exposure, January to April 2013. Euro Surveill 18:20478. DOI: https://doi.org/10.2807/ese.18.19.20478-en

Sala C, Mordhorst H, Grützke J, Brinkmann A, Petersen TN, Poulsen C, Cotter PD, Crispie F, Ellis RJ, Castellani G, Amid C, Hakhverdyan M, Guyader S Le, Manfreda G, Mossong J, Nitsche A, Ragimbeau C, Schaeffer J, Schlundt J, Tay MYF, Aarestrup FM, Hendriksen RS, Pamp SJ, De Cesare A, 2020. Metagenomics-based proficiency test of smoked salmon spiked with a mock community. Microorganisms 8:1861. DOI: https://doi.org/10.3390/microorganisms8121861

Sharma V, Khan MM, 2025. Current Progress and Future Perspective of Chlamydia trachomatis In-fection: A Rising Threat to Women Health. Curr Microbiol 82:314. DOI: https://doi.org/10.1007/s00284-025-04287-x

Shaw KA, Szablewski CM, Kellner S, Kornegay L, Bair P, Brennan S, Kunkes A, Davis M, McGovern OL, Winchell J, Kobayashi M, Burton N, de Perio MA, Gabel J, Drenzek C, Mur-phy J, Holsinger C, Forlano L, 2019. Psittacosis outbreak among workers at chicken slaughter plants, Virginia and Georgia, USA, 2018. Emerg Infect Dis 25:2143-5. DOI: https://doi.org/10.3201/eid2511.190703

Stokes HS, Berg ML, Bennett ATD, 2021. A review of Chlamydial infections in wild birds. Patho-gens 10:948. DOI: https://doi.org/10.3390/pathogens10080948

Vorimore F, Thébault A, Poisson S, Cléva D, Robineau J, de Barbeyrac B, Durand B, Laroucau K, 2015. Chlamydia psittaci in ducks: a hidden health risk for poultry workers. Pathog Dis 73:1-9. DOI: https://doi.org/10.1093/femspd/ftu016

Wallensten A, Fredlund H, Runehagen A, 2014. Multiple human-to-human transmission from a se-vere case of psittacosis, Sweden, January-February 2013. Euro Surveill 19:20937. DOI: https://doi.org/10.2807/1560-7917.ES2014.19.42.20937

Zaręba-Marchewka K, Szymańska-Czerwińska M, Niemczuk K, 2020. Chlamydiae - what’s New? J Vet Res 64; 461-7. DOI: https://doi.org/10.2478/jvetres-2020-0077

Zhang S, Fu Y, Fang L, Xu Q, Gu S, Zhou H, Zhou J, 2025. Psittacosis pneumonia with the reversed halo sign: a case report and literature review. BMC Infect Dis 25:717. DOI: https://doi.org/10.1186/s12879-025-11081-4

CRediT authorship contribution

Yitagele Terefe Mekonnen: writing – original draft, methodology, investigation. Valentina Indio: writing – original draft, formal analysis, data curation. Alex Lucchi: writing – re- view and editing, investigation. Gerardo Manfreda: writing – review and editing. Andrea Serraino: writing – review and editing. Alessandra De Cesare: writing – original draft, conceptualization, methodology, project administration.

How to Cite



1.
Detection of Chlamydia ibidis in the neck skin microbiome of broiler carcasses at the end of slaughter. Ital J Food Safety [Internet]. 2026 Mar. 4 [cited 2026 May 22];. Available from: https://www.pagepressjournals.org/ijfs/article/view/14726