Section: Avian Bacteria

Bacteria on Chicken: Common Pathogens and Mitigation in Poultry Production

Introduction

Poultry production faces persistent challenges from bacterial pathogens that colonize the gastrointestinal tract, respiratory system, and integument of chickens, leading to clinical disease, reduced productivity, and contamination of meat and eggs [1, 2]. These pathogens include both obligate and opportunistic bacteria that exploit management practices, host genetics, and environmental conditions [3, 4]. The economic impact of bacterial diseases in commercial broiler and layer operations is substantial, encompassing mortality, medication costs, and condemnation at slaughter [1, 5]. Moreover, the emergence of antimicrobial resistance (AMR) in poultry-associated bacteria has intensified the need for integrated mitigation strategies that reduce pathogen load without relying solely on antibiotics [2, 6]. This article provides a detailed review of the most common bacterial pathogens found on chickens, their pathogenesis, and the current approaches to their control in poultry production systems.

Common Bacterial Pathogens on Chickens

Salmonella enterica

Salmonella enterica is a major foodborne pathogen associated with poultry products [7, 8]. In chickens, infection can be asymptomatic or cause clinical salmonellosis characterized by diarrhea, septicemia, and mortality, particularly in young birds [9]. The bacterium colonizes the ceca and invades intestinal epithelial cells, leading to systemic spread [10]. Serovars such as Salmonella Enteritidis and Salmonella Typhimurium are frequently isolated from broiler flocks and retail chicken meat [11, 12]. Molecular characterization using whole-genome sequencing has revealed the dissemination of multidrug-resistant (MDR) clones along the production chain [13]. The presence of the invA gene is a key marker for pathogenicity, and its detection via PCR is standard for identification [14]. Mitigation includes vaccination, competitive exclusion products, and strict biosecurity [15, 16].

Campylobacter jejuni and Campylobacter coli

Campylobacter species, particularly C. jejuni and C. coli, are commensal inhabitants of the chicken intestinal tract but are the leading bacterial cause of human foodborne illness [17, 18]. Colonization occurs rapidly in broiler flocks, with horizontal transmission through contaminated water, feed, and litter [19]. Campylobacter does not cause clinical disease in chickens, but its high prevalence in retail meat poses a public health risk [20]. Genomic studies have demonstrated clonal spread of Campylobacter within farms and its association with human infections [21]. Control measures include improved hygiene, bacteriophage therapy, and feed additives such as organic acids [22, 23].

Clostridium perfringens

Clostridium perfringens is a Gram-positive, spore-forming anaerobe that causes necrotic enteritis (NE) in broiler chickens, a disease of major economic importance [2, 24]. NE is often precipitated by predisposing factors such as coccidiosis (Eimeria spp.) or dietary changes that disrupt the intestinal microbiota [25, 26]. The bacterium produces several toxins, including alpha toxin and NetB toxin, which damage the intestinal mucosa and lead to necrosis [2, 27]. Subclinical NE results in reduced feed conversion and growth performance [28]. Control strategies have shifted from antibiotic growth promoters to alternatives such as probiotics, prebiotics, organic acids, and vaccines [2, 29]. Recombinant Lactobacillus vectors delivering nanobodies against NetB and alpha toxin have shown promise in experimental models [30].

Avian Pathogenic Escherichia coli (APEC)

Avian pathogenic Escherichia coli (APEC) is the causative agent of colibacillosis, a systemic disease manifesting as airsacculitis, pericarditis, peritonitis, and yolk sac infection in chicks [31, 32]. APEC strains possess virulence genes encoding adhesins (e.g., fimH), iron acquisition systems (e.g., iutA, fyuA), and immune evasion factors (e.g., iss) [33]. These genes are often carried on mobile genetic elements, facilitating the spread of MDR clones [34]. APEC shares genetic similarities with human extraintestinal pathogenic E. coli (ExPEC), raising zoonotic concerns [35]. Mitigation includes biosecurity, vaccination, and the use of probiotics such as Lactiplantibacillus plantarum [36, 37]. Bacteriophage therapy has also been investigated for controlling APEC infections [38].

Other Bacterial Pathogens

Several other bacteria are commonly isolated from chickens and contribute to disease or contamination. Staphylococcus aureus causes bumblefoot and osteomyelitis, particularly in broilers with lameness [39, 40]. Enterococcus faecalis and Enterococcus cecorum are associated with sternal bursitis and amyloid arthropathy [41, 42]. Pseudomonas aeruginosa and Proteus mirabilis are opportunistic pathogens found in poultry meat and can carry AMR genes [43, 44]. Mycoplasma gallisepticum and Mycoplasma synoviae are important respiratory pathogens that also affect egg production and cause synovitis [45, 46]. Avibacterium paragallinarum causes infectious coryza, a respiratory disease with significant economic impact [47, 48]. Pasteurella multocida is the agent of fowl cholera, a septicemic disease in chickens and turkeys [49, 50].

Mitigation Strategies in Poultry Production

Biosecurity and Management

Biosecurity is the cornerstone of bacterial pathogen control in poultry operations [1, 51]. Measures include all-in/all-out production, cleaning and disinfection of houses, control of rodents and insects, and restricted access for personnel and equipment [52]. Litter management is critical because reused litter can harbor pathogens such as Salmonella and Campylobacter [53, 54]. Water quality and biofilm control in drinking lines also reduce bacterial load [55].

Vaccination

Vaccines are available for several bacterial pathogens. Live and inactivated vaccines against Salmonella Enteritidis and Salmonella Typhimurium are used in layers and breeders [15, 56]. Autogenous vaccines for APEC are employed in some flocks [57]. Vaccination against Clostridium perfringens toxins (toxoid vaccines) can reduce NE severity [2]. For Mycoplasma gallisepticum, live attenuated vaccines (e.g., ts-11) are used in layers [58]. However, vaccine efficacy can be variable, and strain diversity requires ongoing surveillance [59].

Probiotics, Prebiotics, and Synbiotics

Probiotics, particularly Lactobacillus and Bacillus species, are widely used to improve gut health and exclude pathogens [60, 61]. They compete for adhesion sites, produce antimicrobial metabolites, and modulate the immune response [62]. Prebiotics such as mannan-oligosaccharides and fructo-oligosaccharides promote beneficial microbiota [63]. Synbiotics combine both approaches and have shown efficacy against Salmonella and Campylobacter colonization [64, 65].

Organic Acids and Phytogenics

Organic acids (e.g., formic, propionic, butyric acids) are added to feed or water to reduce pH and inhibit pathogen growth [66]. Butyric acid also supports intestinal epithelial integrity [67]. Phytogenic feed additives, including essential oils and plant extracts, possess antimicrobial and anti-inflammatory properties [68, 69]. Their mechanisms include disruption of bacterial cell membranes and modulation of gut microbiota [70].

Bacteriophage Therapy

Bacteriophages are viruses that specifically lyse bacterial cells. They have been investigated for controlling Salmonella, Campylobacter, and APEC in poultry [71, 72]. Phage cocktails can be applied via feed, water, or spray to reduce pathogen load on carcasses [73]. Challenges include phage stability, narrow host range, and the potential for bacterial resistance [74].

Antimicrobial Stewardship

The reduction of antibiotic use in poultry is a global priority to combat AMR [75]. Alternatives such as those described above are increasingly adopted. When antibiotics are necessary, culture and susceptibility testing should guide selection [76]. Monitoring of AMR genes through genomic surveillance is essential for detecting emerging resistance [77, 78].

Diagnostic Approaches

Accurate diagnosis of bacterial infections in poultry relies on culture, molecular methods, and serology [79]. Matrix-assisted laser desorption/ionization time-of-flight (MALDI-TOF) mass spectrometry enables rapid species identification [14]. PCR and quantitative PCR (qPCR) are used for detecting specific pathogens and virulence genes [80, 81]. Multiplex qPCR assays can differentiate wild-type from vaccine strains (e.g., for Mycoplasma gallisepticum) [82]. Whole-genome sequencing provides detailed information on serovars, AMR genes, and phylogenetic relationships [83, 84]. For field deployment, isothermal amplification methods such as recombinase-aided amplification (RAA) combined with CRISPR/Cas12a have been developed for Mycoplasma detection [85, 86].

Integrated Pathogen Management Decision Tree

The following Mermaid diagram illustrates a decision framework for managing bacterial pathogens in broiler production.

flowchart TD
    A["Start: Flock Health Assessment"] --> B{Clinical signs present?}
    B -->|Yes| C[Perform necropsy and laboratory diagnostics]
    B -->|No| D[Implement routine biosecurity and monitoring]
    C --> E{Pathogen identified?}
    E -->|Salmonella| F[Vaccination + competitive exclusion + hygiene]
    E -->|Campylobacter| G[Bacteriophage + organic acids + litter management]
    E -->|Clostridium perfringens| H[Probiotics + coccidiosis control + toxin vaccine]
    E -->|APEC| I[Autogenous vaccine + biosecurity + phage therapy]
    E -->|Other| J[Targeted antimicrobial therapy based on AST]
    F --> K[Monitor AMR and adjust strategy]
    G --> K
    H --> K
    I --> K
    J --> K
    D --> L["Regular surveillance (culture, PCR, WGS")]
    L --> M{Pathogen detected?}
    M -->|Yes| N[Implement targeted mitigation]
    M -->|No| O[Continue routine management]
    N --> K
    O --> P[Review and update biosecurity protocols]
    P --> A

Conclusion

Bacterial pathogens on chickens represent a complex challenge requiring multifaceted mitigation approaches. Salmonella, Campylobacter, Clostridium perfringens, and APEC are the most significant in terms of disease burden and food safety. Integrated strategies combining biosecurity, vaccination, probiotics, organic acids, bacteriophages, and antimicrobial stewardship are essential for sustainable poultry production. Advances in molecular diagnostics and genomics enable precise pathogen identification and surveillance, supporting evidence-based interventions. Continued research into host-pathogen interactions and novel control measures will further reduce the impact of these bacteria on poultry health and public health.

References

[1] Fasina Y, Suarez DL, Ritter GD, et al. Unraveling frontiers in poultry health (part 1) – Mitigating economically important viral and bacterial diseases in commercial Chicken and Turkey production. Poultry Science. 2024. URL: https://www.semanticscholar.org/paper/fbfef3fa6f334870f2fbd2fe3339be334a7c7006

[2] Villagrán-de la Mora Z, Macías-Rodríguez ME, Arratia-Quijada J, et al. Clostridium perfringens as Foodborne Pathogen in Broiler Production: Pathophysiology and Potential Strategies for Controlling Necrotic Enteritis. Animals. 2020. URL: https://www.semanticscholar.org/paper/bb36940ad89938ae8aebbe98355429410804b6f1

[3] Shange R, Ankumah R, Zabawa R, et al. Bacterial Community Structure and Composition in Soils under Industrial Poultry Production Activities: An Observational study. Journal. 2013. URL: https://www.semanticscholar.org/paper/defb1f108883ad6cc1c45cb4eb7398539b00d829

[4] Gómez-Osorio L, Chaparro-Gutiérrez J, López-Osorio S. Nutrition and Poultry Coccidiosis: Causes, Consequences and Current Strategies to Modulate the Disease. Advances in Poultry Nutrition Research. 2021. URL: https://www.semanticscholar.org/paper/cfab094034d8d4821984654988680d36401a17dd

[5] Xu J, Tao L, Zhang M, et al. Panaxadiol acts as an HIF-1α inhibitor to suppress H9N2-induced inflammation. Veterinary Microbiology. 2025. URL: https://www.semanticscholar.org/paper/1f08f64d2848ec831763dc177d390aa722ed2afa

[6] Zhang B, Kuang S, He Z, et al. Avian HEV triggered egg decline: Viral-host, immune-neuroendocrine mechanisms in layers. Veterinary Microbiology. 2025. URL: https://www.semanticscholar.org/paper/5e927e11f2960a66ff2b4b2cd7a2ffe9e4f33743

[7] Liu B, Yu H, Yan Z, et al. Identification of thermostability-enhancing mutations in H9N2 avian influenza virus hemagglutinin. Journal of Virology. 2026. URL: https://www.semanticscholar.org/paper/08bd03de5ef23ed146f01aa50afe2e4a98c613d0

[8] O Nyararai Y, Blessing M Ndau, V M, et al. A Review of Avian Pathogenic Escherichia Coli (APEC) in Guinea Fowls (Numida Meleagris) of Southern Africa: Antimicrobial Resistance and Virulence Genomics and Control Strategies. International journal of research and scientific innovation. 2026. URL: https://www.semanticscholar.org/paper/56b965cb044de904e35825ab69a48e9da1b2d48b

[9] Bommineni V, Edison L, Gottapu C, et al. Hepatic Transcriptomic Landscape of Chicken Reveals Host Responses to Spotty Liver Disease. bioRxiv. 2026. URL: https://www.semanticscholar.org/paper/30881c3cae5032a5372499feb685e020a7a6fd95

[10] Asnayanti A, Do A, Alharbi KS, et al. Inducing experimental bacterial chondronecrosis with osteomyelitis lameness in broiler chickens using aerosol transmission model. Poultry Science. 2024. URL: https://www.semanticscholar.org/paper/69753c33dca0de44f99402530c082d1da34db18c

[11] Gangaiah D, Ryan V, Van Hoesel D, et al. Recombinant Limosilactobacillus (Lactobacillus) delivering nanobodies against Clostridium perfringens NetB and alpha toxin confers potential protection from necrotic enteritis. MicrobiologyOpen. 2022. URL: https://www.semanticscholar.org/paper/0a9b9b901a21fb4e7182e50e01d8d4932f75feff

[12] Yan H, Wang G, Zhao R, et al. Biological characterization of an avian leukosis virus subgroup J isolate from yunnan indigenous black-bone chickens and generation of its full-length infectious clone. Archives of Virology. 2026. URL: https://www.semanticscholar.org/paper/187dabae3774fc3cb0d82aa149cb08239fd1e97b

[13] Liu J, Guo J, Whitmore MA, et al. Intestinal Dysbiosis in Necrotic Enteritis: Dissecting the Roles of Eimeria and Clostridium perfringens. bioRxiv. 2026. URL: https://www.semanticscholar.org/paper/a40bd9bd5a21d56abc0cacc66c2ec46035209ad5

[14] Microbiology, induction, and management practices to mitigate lameness caused by bacterial chondronecrosis with osteomyelitis in broiler chickens. German Journal of Veterinary Research. 2024. URL: https://www.semanticscholar.org/paper/21976f87c32731f2f7447f055016c41edf955a39

[15] Wang JY, Bajagai YS, Sajid GA, et al. Transcriptomic analysis reveals a crucial role of the yolk sac during Avian Pathogenic Escherichia coli infection in chicken embryos. Poultry Science. 2026. URL: https://www.semanticscholar.org/paper/e019cfbd7a75ee365ee9fad67612bebc50b88f8d

[16] Mahmoud ME, Ali A, Farooq M, et al. Cyclooxygenase-2/prostaglandin E2 pathway orchestrates the replication of infectious bronchitis virus in chicken tracheal explants. Microbiology spectrum. 2024. URL: https://www.semanticscholar.org/paper/c2ad9689e48e3b46c33e5ade6e4a9a98215366a4

[17] Phytogenics Improve First-line Defence in Swine and Poultry. Journal. 2016. URL: https://www.semanticscholar.org/paper/ee7cf6be7bd4043dc60aee91e13951ad88c497a1

[18] Saleh A, Cho S, Shaban MZ, et al. Effect of dietary supplementation of betaine and organic minerals on growth performance, serum biochemical parameters, nutrients digestibility, and growth-related genes in broilers under heat stress. Poultry Science. 2023. URL: https://www.semanticscholar.org/paper/15d357a9d15fe9162b7d7d963f306e61796215be

[19] Quyen D, Lanh PT, Oanh NK, et al. Isolation and characterization of Salmonella enterica associated with diarrhea in chickens and ducks in Hai Duong province. Vietnam Journal of Biotechnology. 2024. URL: https://www.semanticscholar.org/paper/ccbd403dd1f14b3db4e6d14f8acf3a292ff8b18d

[20] Saleem G. Necrotic enteritis, disease induction, predisposing factors and novel biochemical markers in broilers chickens. Journal. 2013. URL: https://www.semanticscholar.org/paper/e30fe841f5e6c709f2d59d2a46347824ffc9a653

[21] He X, Lu Z, Ma B, et al. Effects of dietary taurine supplementation on growth performance, jejunal morphology, appetite-related hormones, and genes expression in broilers subjected to chronic heat stress. Poult Sci. 2019. URL: https://pubmed.ncbi.nlm.nih.gov/30778570/

[22] Li Y, Xue Y, Quan Y, et al. Direct interaction between avian pathogenic Escherichia coli and H9N2 avian influenza virus promotes bacterial adhesion during their infections. Microbiol Spectr. 2026. URL: https://pubmed.ncbi.nlm.nih.gov/42294695/

[23] Kanwal B, Asif E, Kalhoro NH, et al. Prevalence of Antimicrobial-Resistant Bacterial Pathogens Among Livestock in Subtropical Environments. Antibiotics (Basel). 2026. URL: https://pubmed.ncbi.nlm.nih.gov/42192683/

[24] Kamali SK, Tajbakhsh E, Khamsipour F, et al. Molecular Insights and Antibiotic Resistance of Proteus mirabilis from Retail Meat Sources in Iran. Food Sci Nutr. 2026. URL: https://pubmed.ncbi.nlm.nih.gov/42145818/

[25] Derks MFL, Dibbits B, Crooijmans RPMA, et al. Discovery of Novel Viruses and Common Contaminants From Unmapped DNA and RNA in Pigs and Chickens Under Different Housing Conditions. Anim Genet. 2026. URL: https://pubmed.ncbi.nlm.nih.gov/42126340/

[26] Zaman S, Ali N, Ullah W, et al. Metagenomic Profiling Reveals Extensive Bacterial Diversity in Chicken Manure and Associated Contaminated Wastewater. Int J Mol Sci. 2026. URL: https://pubmed.ncbi.nlm.nih.gov/42123326/

[27] Li Y, Tang H, Chen Y, et al. Emergence of Linezolid Resistance Genes optrA and poxtA in an Avian Enterococcus asini. Int J Mol Sci. 2026. URL: https://pubmed.ncbi.nlm.nih.gov/42123305/

[28] Biswas P, Ahmed S, Mondal S, et al. Recombinant LAB vector-based multicomponent vaccine against Campylobacter jejuni potentially promoting a healthier microbial balance in the poultry gut. Microbiome. 2026. URL: https://pubmed.ncbi.nlm.nih.gov/42098871/

[29] Zhang K, Chen Q, Chen J, et al. Contactless gas-sensitive photoelectrochemical biosensor for determination of Salmonella typhimurium based on SnO(2)/CeO(2) heterojunction. Anal Chim Acta. 2026. URL: https://pubmed.ncbi.nlm.nih.gov/42067303/

[30] Wattrang E, Näslund K, Tamminen LM, et al. Immune parameters monitored during the production period of laying hens managed with or without single-dose vaccination against erysipelas. BMC Vet Res. 2026. URL: https://pubmed.ncbi.nlm.nih.gov/42063043/

[31] Li Y, Quan Y, Quan K, et al. Construction and immunogenicity evaluation of avian Escherichia coli-derived bacterial biomimetic vesicles displaying H9 subtype avian influenza virus HA1 protein. Vet Microbiol. 2026. URL: https://pubmed.ncbi.nlm.nih.gov/42061219/

[32] Song H, Wang J, Hao Y, et al. Gut microbiota dysbiosis induced by tibial dyschondroplasia in turn accelerates disease pathogenesis through the gut-bone axis in broilers. Poult Sci. 2026. URL: https://pubmed.ncbi.nlm.nih.gov/42025006/

[33] Höller P, Asp E, Pärssinen J, et al. Avian influenza and coronaviruses in live animal and wet markets in Laos: prevalence and public health considerations. Front Cell Infect Microbiol. 2026. URL: https://pubmed.ncbi.nlm.nih.gov/42022805/

[34] Ager EO, Nickodem CA, Brown J, et al. Diet-vaccine interactions: SQM Iron and Salmonella vaccination shape poultry gut microbiota. Appl Environ Microbiol. 2026. URL: https://pubmed.ncbi.nlm.nih.gov/41979594/

[35] Wu L, Li P, Bai M, et al. Whole-genome analysis of a polyvalent Salmonella phage reveals its potential to combat intracellular infection and food contamination. Food Res Int. 2026. URL: https://pubmed.ncbi.nlm.nih.gov/41942208/

[36] Akrami F, Jamali H, Houle S, et al. Host range and zoonotic potential linked to P-like fimbrial (PLF) adhesin specificity in avian pathogenic Escherichia coli. PLoS Pathog. 2026. URL: https://pubmed.ncbi.nlm.nih.gov/41941531/

[37] Shaufi MAM, Chia SL, Hassim HA, et al. Effect of bacteriophages on growth performance and health indicators in broiler chickens in the absence of bacterial challenge - A review. Vet Med (Praha). 2026. URL: https://pubmed.ncbi.nlm.nih.gov/41869088/

[38] Xu T, Yang W, Cao J, et al. Isolation and therapeutic potential of phage vB_EcoM_GXW16 against a drug-resistant avian pathogenic Escherichia coli strain. Poult Sci. 2026. URL: https://pubmed.ncbi.nlm.nih.gov/41833115/

[39] Zhang Y, Chu M, Samala S, et al. Mobile genetic elements drive the evolution and multidrug resistance of Salmonella infantis along the United States poultry production line. BMC Genomics. 2026. URL: https://pubmed.ncbi.nlm.nih.gov/41776394/

[40] El-Shall NA, Adiguzel MC, Abd El-Ghany WA, et al. Salmonella infection in chickens: pathogen, pathogenesis, and dietary non-drug feed additives as alternatives to antibiotics - a comprehensive review. Folia Microbiol (Praha). 2026. URL: https://pubmed.ncbi.nlm.nih.gov/41762430/

[41] Ribeiro J, Silva V, Pinto P, et al. Genomic and phenotypic characterization


Disclaimer: This article is for educational and informational purposes only. It is not intended to substitute for professional veterinary advice, diagnosis, treatment, or regulatory guidance. Always consult a licensed veterinarian or qualified specialist regarding animal health, disease diagnosis, and therapeutic decisions.