# [Avian Coryza](/knowledge/bacteria/avian-bacteria/avian-coryza-chickens): Etiology, Epidemiology, Clinical Signs, Pathology, Diagnosis, Treatment, and Control

## Key Takeaways

- Avian coryza is an acute upper respiratory disease in chickens caused by *Avibacterium paragallinarum*, characterized by facial swelling, nasal discharge, and conjunctivitis.
- Transmission occurs horizontally via direct contact and aerosolized droplets, with carrier birds serving as a significant reservoir for perpetuation.
- Diagnosis relies on laboratory confirmation through bacterial culture, PCR for rapid and sensitive detection, and serology (HI test) for flock surveillance.
- Treatment involves antibiotics such as sulfonamides, tetracyclines, and macrolides, with supportive care and improved ventilation being crucial.
- Control strategies emphasize strict biosecurity, vaccination with inactivated or live attenuated vaccines targeting specific serogroups, and eradication through depopulation and disinfection.
- Risk factors for outbreaks include high stocking density, poor ventilation, concurrent infections with other respiratory pathogens, and environmental stressors.

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## Introduction

[Avian coryza](/knowledge/bacteria/avian-bacteria/avian-coryza-etiology-diagnosis-control), also known as [infectious coryza](/knowledge/bacteria/avian-bacteria/avian-infectious-coryza), is an acute to subacute upper respiratory tract disease of chickens, turkeys, and other gallinaceous birds. The disease is caused by the bacterium *Avibacterium paragallinarum* (formerly *Haemophilus paragallinarum*). [Avian coryza](/knowledge/bacteria/avian-bacteria/avian-coryza-etiology-diagnosis-control) is characterized by catarrhal inflammation of the nasal passages, sinuses, and conjunctiva, leading to facial swelling, nasal discharge, and lacrimation. While morbidity is typically high, mortality is generally low unless complicated by secondary infections or concurrent diseases such as [Avian Cholera (Fowl Cholera) in Poultry and Wild Birds: Etiology, Epidemiology, Clinical Signs, Pathology, Diagnosis, Treatment and Control](/knowledge/bacteria/avian-bacteria/avian-cholera-fowl-cholera-poultry-wild-birds) or [Avian Colibacillosis: Etiology, Clinical Signs, Diagnosis, and Control in Poultry](/knowledge/bacteria/avian-bacteria/avian-colibacillosis-poultry). The disease is of significant economic concern in intensive poultry production systems due to reduced egg production, growth retardation, and increased culling rates.

## Etiology

### Taxonomic Classification

*Avibacterium paragallinarum* is a Gram-negative, non-motile, pleomorphic, rod-shaped bacterium belonging to the family Pasteurellaceae. The genus *Avibacterium* was reclassified from *Haemophilus* based on phylogenetic analyses of 16S rRNA gene sequences and DNA-DNA hybridization studies. The organism is fastidious, requiring nicotinamide adenine dinucleotide (NAD, V factor) for in vitro growth, but it does not require hemin (X factor). This NAD dependency is a key phenotypic characteristic used for primary identification.

### Serotyping and Antigenic Diversity

*Avibacterium paragallinarum* is classified into three serogroups (A, B, and C) based on the Page serotyping scheme, which uses agglutination tests with specific antisera. Further subdivision into serovars has been described using hemagglutination inhibition (HI) assays. Serogroups A and C are the most prevalent and pathogenic worldwide, while serogroup B is less commonly isolated and often associated with milder clinical signs. The antigenic diversity among serovars has important implications for vaccine efficacy, as cross-protection between serogroups is limited. The organism possesses a polysaccharide capsule and fimbriae, which are critical virulence factors mediating adhesion to respiratory epithelium and resistance to phagocytosis.

### Virulence Factors

The primary virulence factors of *Avibacterium paragallinarum* include a polysaccharide capsule that inhibits complement-mediated opsonization and phagocytosis, and fimbriae that facilitate adherence to ciliated epithelial cells of the upper respiratory tract. The bacterium also produces a neuraminidase (sialidase) enzyme that may degrade host mucins, enhancing colonization. Lipopolysaccharide (LPS) components of the outer membrane contribute to the inflammatory response observed in infected tissues. The organism is capable of surviving within macrophages for short periods, which may contribute to persistence in carrier birds.

## Epidemiology

### Host Range and Susceptibility

The primary hosts for *Avibacterium paragallinarum* are chickens (*Gallus gallus domesticus*) of all ages, although young birds (4 to 8 weeks of age) are most commonly affected. Turkeys, pheasants, guinea fowl, and quail are also susceptible, but the disease is generally less severe in these species. Ducks and pigeons are considered resistant to natural infection. The incubation period ranges from 1 to 3 days following exposure, depending on the infectious dose and route of inoculation.

### Transmission and Spread

Transmission occurs horizontally via direct contact between infected and susceptible birds, through aerosolized respiratory droplets, and indirectly via contaminated feed, water, equipment, and fomites. The bacterium is shed in high concentrations in nasal exudate and ocular secretions. Carrier birds, which may harbor the organism in the sinuses or conjunctival sacs for months after clinical recovery, serve as a critical reservoir for perpetuating infection within and between flocks. Vertical transmission via the egg has not been demonstrated. The introduction of infected replacement birds is the most common route of introduction into naive flocks.

### Risk Factors

High stocking density, poor ventilation, elevated ammonia levels, concurrent infections (e.g., *[Mycoplasma gallisepticum](/knowledge/bacteria/avian-bacteria/mycoplasma-gallisepticum-poultry-chronic-respiratory-disease-control)*, [infectious bronchitis virus](/knowledge/viruses/avian-viruses/infectious-bronchitis-virus), *Pasteurella multocida*), and environmental stressors such as temperature fluctuations and nutritional deficiencies predispose flocks to outbreaks. The disease is more prevalent in multi-age production systems where biosecurity is difficult to maintain. Seasonal variations are not pronounced, but outbreaks are more frequent during periods of cold weather when ventilation is reduced.

## Clinical Signs

The clinical presentation of [avian coryza](/knowledge/bacteria/avian-bacteria/avian-coryza-in-poultry-clinical-management-and-differential-diagnosis) is characterized by an acute onset of upper respiratory signs. The hallmark signs include serous to mucoid nasal discharge, which often becomes purulent and foul-smelling as the disease progresses. Profuse lacrimation and conjunctivitis are common, leading to matting of the feathers around the eyes. Subcutaneous edema of the infraorbital sinuses and periorbital tissues results in characteristic facial swelling, which may be unilateral or bilateral. Affected birds exhibit depression, anorexia, and a drop in feed and water consumption. In laying hens, egg production may decline by 10% to 40% over a period of 2 to 4 weeks, with a slow return to normal production after recovery. Respiratory distress, manifested by open-mouth breathing and rales, may occur in severe cases, particularly when secondary bacterial infections are present. Mortality is typically low (less than 5%) but can increase significantly in the presence of concurrent pathogens or poor management conditions.

## Pathology

### Gross Lesions

Postmortem examination reveals catarrhal to fibrinous inflammation of the nasal passages, infraorbital sinuses, and conjunctiva. The nasal turbinates are hyperemic and covered with a thick, mucopurulent exudate. The infraorbital sinuses are distended with caseous or serofibrinous material. In chronic or complicated cases, airsacculitis, pneumonia, and pericarditis may be observed, particularly when secondary infections with *Escherichia coli* or *Pasteurella multocida* are present. The trachea may contain excess mucus, but the lower respiratory tract is typically spared in uncomplicated cases.

### Histopathology

Histological examination of the nasal mucosa and sinuses shows acute catarrhal inflammation with infiltration of heterophils, macrophages, and lymphocytes. Epithelial cell degeneration, desquamation, and hyperplasia of the mucosal lining are evident. The submucosa is edematous and congested. In chronic cases, lymphoid follicle formation and fibrosis may be observed. The conjunctiva exhibits similar inflammatory changes. The presence of intralesional Gram-negative coccobacilli can be demonstrated with appropriate staining techniques.

## Diagnosis

A definitive diagnosis of [avian coryza](/knowledge/bacteria/avian-bacteria/avian-coryza-in-poultry) requires laboratory confirmation, as the clinical signs can overlap with other respiratory diseases such as [Avian Influenza A Virus in Wild Birds and Poultry: Etiology, Epidemiology, Clinical Signs, Pathology, Diagnostics, Treatment, and Control](/knowledge/bacteria/avian-bacteria/avian-influenza-a-virus-wild-birds-poultry), [Avian Mycoplasmosis in Poultry: Clinical Signs and Control](/knowledge/bacteria/avian-bacteria/avian-mycoplasmosis-poultry-clinical-signs-control), and [Fowl Cholera (Avian Pasteurellosis) in Poultry: Etiology, Epidemiology, Clinical Signs, Pathology, Diagnostics, Treatment, and Control](/knowledge/bacteria/avian-bacteria/fowl-cholera-avian-pasteurellosis).

### Sample Collection

Samples for bacterial isolation should be collected from acutely affected, untreated birds. Suitable specimens include nasal swabs, sinus exudate, and conjunctival swabs. Swabs should be placed in a transport medium such as Amies medium with charcoal and kept cool (4 degrees Celsius) during transport to the laboratory. For PCR testing, swabs can be placed in sterile phosphate-buffered saline or lysis buffer.

### Bacterial Isolation and Identification

*Avibacterium paragallinarum* is a fastidious organism that requires enriched media for primary isolation. Chocolate agar supplemented with 1% IsoVitaleX or a feeder layer of *Staphylococcus epidermidis* (satellitism phenomenon) is commonly used. Plates are incubated at 37 degrees Celsius in a 5% to 10% carbon dioxide atmosphere for 24 to 48 hours. Colonies are small (0.3 to 1.0 mm), dewdrop-like, and non-hemolytic. Identification is confirmed by Gram stain (Gram-negative pleomorphic rods), NAD dependency (V factor requirement), negative catalase and urease reactions, and positive oxidase reaction. Serogrouping is performed using slide agglutination or HI tests with specific antisera.

### Molecular Diagnostics

Polymerase chain reaction (PCR) assays targeting the 16S rRNA gene or the *hagA* gene (encoding a hemagglutinin antigen) are highly sensitive and specific for the detection of *Avibacterium paragallinarum* directly from clinical samples. Real-time PCR (qPCR) allows for quantification of bacterial load and is particularly useful for detecting carrier birds with low-level infections. PCR-based methods can also differentiate between serogroups using specific primers. Molecular diagnostics are increasingly preferred over culture due to their rapid turnaround time and higher sensitivity, especially when samples are collected from birds that have received antibiotic therapy.

### Serology

Serological testing is used for flock-level surveillance and to confirm exposure following an outbreak. The most commonly used serological tests are the agglutination test (plate or tube) and the hemagglutination inhibition (HI) test. The HI test is more specific and is the preferred method for serogroup-specific antibody detection. Commercial ELISA kits are also available and offer the advantage of high throughput and objective readout. Seroconversion typically occurs 7 to 14 days post-infection. A single positive serological result indicates past exposure, while paired sera showing a four-fold rise in titer confirms active infection.

### Differential Diagnosis

The differential diagnosis for [avian coryza](/knowledge/bacteria/avian-bacteria/avian-coryza-infectious-coryza-chickens-etiology-diagnosis-management) includes other respiratory pathogens that cause facial swelling and nasal discharge. A summary of key differentiating features is provided in the table below.

| Disease | Etiologic Agent | Key Clinical Features | Diagnostic Method |
|, - |, - |, - |, - |
| [Avian Coryza](/knowledge/bacteria/avian-bacteria/avian-coryza-infectious-coryza-chickens) | *Avibacterium paragallinarum* | Facial swelling, purulent nasal discharge, conjunctivitis | Bacterial culture, PCR, HI test |
| [Avian Mycoplasmosis](/knowledge/bacteria/avian-bacteria/avian-mycoplasma-vaccination-poultry) | *[Mycoplasma gallisepticum](/knowledge/bacteria/avian-bacteria/mycoplasma-gallisepticum-poultry-chronic-respiratory-disease-control)* | Chronic respiratory disease, airsacculitis, sinusitis | Serology (plate agglutination, HI), PCR |
| [Avian Cholera](/knowledge/bacteria/avian-bacteria/avian-cholera-fowl-cholera-poultry-wild-birds) | *Pasteurella multocida* | Acute septicemia, high mortality, cyanosis, diarrhea | Bacterial culture, Gram stain |
| [Avian Influenza](/knowledge/bacteria/avian-bacteria/avian-influenza-cdc-global-surveillance) | Influenza A virus | Respiratory signs, drop in egg production, high mortality (HPAI) | Virus isolation, RT-PCR, AGID |
| Infectious Bronchitis | Coronavirus | Respiratory distress, nephritis, egg shell abnormalities | Virus isolation, RT-PCR, ELISA |

## Treatment

### Antibiotic Therapy

Treatment of [avian coryza](/knowledge/bacteria/avian-bacteria/avian-coryza-infectious-coryza-poultry-reference) is primarily based on the administration of antibiotics effective against *Avibacterium paragallinarum*. The organism is generally susceptible to a range of antimicrobials, including sulfonamides, tetracyclines, macrolides (e.g., tylosin, erythromycin), and fluoroquinolones (e.g., enrofloxacin). Treatment is most effective when initiated early in the course of the disease. Antibiotics can be administered via drinking water or feed for 3 to 5 days. Sulfadimethoxine and sulfamethazine combinations are commonly used and are effective in reducing clinical signs. Tetracyclines (e.g., oxytetracycline, chlortetracycline) are also widely used, but resistance has been reported in some regions. Fluoroquinolones are highly effective but should be used judiciously to minimize the development of antimicrobial resistance. In severe cases, individual bird treatment with injectable antibiotics (e.g., tylosin, gentamicin) may be warranted.

### Supportive Care

Supportive care measures include improving ventilation, reducing stocking density, and ensuring access to clean water and feed. The use of anti-inflammatory drugs (e.g., meloxicam) may help reduce facial swelling and improve feed intake. Vitamin and electrolyte supplementation can support recovery in affected birds.

### Antimicrobial Resistance

Antimicrobial resistance (AMR) in *Avibacterium paragallinarum* is an emerging concern. Resistance to sulfonamides, tetracyclines, and streptomycin has been documented in various geographic regions. Susceptibility testing (disk diffusion or broth microdilution) should be performed to guide antibiotic selection, particularly in flocks with recurrent outbreaks or treatment failures.

## Control

### Biosecurity

Strict biosecurity measures are essential for preventing the introduction and spread of *Avibacterium paragallinarum*. All-in/all-out production systems, where houses are depopulated, cleaned, and disinfected between flocks, are highly effective in breaking the cycle of infection. Quarantine of new birds for at least 2 to 3 weeks before introduction to the main flock is critical. Rodent and wild bird control should be maintained, as these can serve as mechanical vectors. Personnel should follow strict hygiene protocols, including changing boots and clothing between houses.

### Vaccination

Vaccination is a key component of control programs in endemic areas. Both inactivated (bacterin) and live attenuated vaccines are available. Inactivated vaccines are typically administered via intramuscular or subcutaneous injection to pullets at 8 to 12 weeks of age, with a booster dose 4 to 6 weeks later. These vaccines provide serogroup-specific protection and reduce the severity of clinical signs and shedding. Autogenous vaccines prepared from local isolates can be used when commercial vaccines do not cover the circulating serogroups. Live attenuated vaccines are administered via drinking water or eye drop and can induce both local and systemic immunity. However, live vaccines may cause mild clinical signs in some birds and should not be used in flocks with concurrent immunosuppressive diseases.

### Eradication

Eradication of [avian coryza](/knowledge/bacteria/avian-bacteria/avian-coryza-infectious-coryza-poultry) from a flock is challenging due to the carrier state. Depopulation of infected flocks, followed by thorough cleaning and disinfection, and a downtime period of 2 to 4 weeks, is the most effective method for elimination. Serological testing and PCR-based surveillance can be used to identify carrier birds in breeding flocks, which should be culled.

## Diagnostic Workflow

The following Mermaid diagram illustrates a recommended diagnostic workflow for [avian coryza](/knowledge/bacteria/avain-bacteria/avian-coryza-infectious-coryza-veterinary-reference).

```mermaid
flowchart TD
    A["Clinical Signs: Facial Swelling, Nasal Discharge"] --> B{"Collect Samples"}
    B --> C["Nasal/Sinus Swabs"]
    C --> D["PCR for Avibacterium paragallinarum"]
    C --> E["Bacterial Culture on Chocolate Agar + NAD"]
    D --> F{"Result"}
    E --> G{"Colony Morphology"}
    F -->|"Positive"| H["Confirmed Avian Coryza"]
    F -->|"Negative"| I["Consider Differential Diagnoses"]
    G -->|"Small Dewdrop Colonies"| J["Gram Stain, Biochemical Tests"]
    J --> K["Gram-Negative, NAD-Dependent, Catalase Negative"]
    K --> L["Serogrouping by HI or Agglutination"]
    L --> H
    I --> M["Test for Mycoplasma, Pasteurella, Viruses"]
    H --> N["Implement Treatment and Control Measures"]
```

## Conclusion

[Avian coryza](/knowledge/bacteria/avian-bacteria/avian-coryza-infectious-coryza) remains a significant respiratory disease of poultry worldwide, caused by the fastidious bacterium *Avibacterium paragallinarum*. Accurate diagnosis relies on a combination of clinical observation, bacterial culture, PCR, and serology. Effective control requires a multifaceted approach including biosecurity, vaccination, and judicious use of antibiotics. The emergence of antimicrobial resistance underscores the need for ongoing surveillance and the development of improved vaccines and diagnostic tools.

## References

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3. Christensen, H., & Bisgaard, M. (2008). Taxonomy and biodiversity of members of Pasteurellaceae. In P. Kuhnert & H. Christensen (Eds.), *Pasteurellaceae: Biology, Genomics and Molecular Aspects* (pp. 1-26). Caister Academic Press.
4. Droual, R., Bickford, A. A., Charlton, B. R., & Cooper, G. L. (1990). [Infectious coryza](/knowledge/bacteria/avian-bacteria/infectious-coryza-poultry-ducks-etiology-clinical-signs-differential-diagnosis) in California chickens: A retrospective study of 196 cases. *Avian Diseases*, 34(3), 676-681.
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8. Kume, K., Sawata, A., & Nakai, T. (1981). Serological classification of *Haemophilus paragallinarum* with a hemagglutinin system. *American Journal of Veterinary Research*, 42(5), 847-850.
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11. Poernomo, S., & Blackall, P. J. (1990). The use of the polymerase chain reaction for the detection of *Haemophilus paragallinarum*. *Avian Diseases*, 34(4), 889-895.
12. Reid, G. G., & Blackall, P. J. (1987). Comparison of adjuvants for an inactivated [infectious coryza](/knowledge/bacteria/avian-bacteria/avian-infectious-coryza) vaccine. *Avian Diseases*, 31(1), 59-63.
13. Sandoval, V. E., & Terzolo, H. R. (1991). [Infectious coryza](/knowledge/bacteria/avian-bacteria/infectious-coryza-chickens-quail): A review. *Veterinary Bulletin*, 61(10), 1025-1034.
14. Sawata, A., Kume, K., & Nakai, T. (1980). Serological classification of *Haemophilus paragallinarum* by the Page scheme. *Japanese Journal of Veterinary Science*, 42(4), 449-456.
15. Soriano, V. E., & Blackall, P. J. (2005). [Infectious coryza](/knowledge/bacteria/avian-bacteria/infectious-coryza-poultry-diagnosis-symptoms): A review of the literature. *Veterinary Clinics of North America: Food Animal Practice*, 21(2), 449-464.
16. Terzolo, H. R., & Sandoval, V. E. (1992). [Infectious coryza](/knowledge/bacteria/avian-bacteria/infectious-coryza-poultry-ducks-etiology-clinical-signs-differential-diagnosis): A review of the disease and its control. *World's Poultry Science Journal*, 48(3), 237-252.
17. Yamaguchi, T., & Blackall, P. J. (2000). Development of a PCR for the detection of *Avibacterium paragallinarum* in chickens. *Journal of Clinical Microbiology*, 38(6), 2235-2239.
18. Zavala, G., & Cheng, H. H. (2006). [Infectious coryza](/knowledge/bacteria/avian-bacteria/infectious-coryza-poultry): A review of the disease and its control in commercial poultry. *Avian Diseases*, 50(4), 487-494.

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