Bordetella avium

Last updated

Bordetella avium
Scientific classification OOjs UI icon edit-ltr.svg
Domain: Bacteria
Phylum: Pseudomonadota
Class: Betaproteobacteria
Order: Burkholderiales
Family: Alcaligenaceae
Genus: Bordetella
Species:
B. avium
Binomial name
Bordetella avium
Kersters et al. 1984 [1]
Type strain
197N, ATCC BAA-1003 [2]

Bordetella avium is a gram negative, nonfermentative, strictly aerobic, motile bacterium from the genus Bordetella which has been isolated from patients with respiratory disease (cystic fibrosis). [3] [4] [5] B. avium has a global distribution, that mainly affects young domesticated turkeys. [6] [7] The disease in birds is called bordetellosis, and is largely associated with confined spaces and multi-aged flocks where management practices are sub optimal. In most infections, mortality is typically low but morbidity is very high. [8] [9]

Contents

The pathogenesis of B. avium is through fimbrial attachment to the respiratory epithelium and release of a variety of virulence factors, leading to respiratory symptoms, such as sneezing, ocular and nasal discharge, and inflammation. Further complications include edema, tracheal collapse, and decreased growth rate. Bordetellosis has a major impact on turkey health within turkey production systems but the impact in wild birds is not yet well defined. Good management practice and biosecurity protocols are essential for controlling disease caused by B. avium as the efficacy of antibiotics treatments for disease are variable, and prevention with vaccinations may not provide complete protection. [6] [7] [8] [10] [11]

Microbial Characteristics

Barnyard turkey flock, photographed in Saskatchewan, Canada. Turkeys are the primary domestic species affected by Bordetella avium. Male Turkey.png
Barnyard turkey flock, photographed in Saskatchewan, Canada. Turkeys are the primary domestic species affected by Bordetella avium.

Bordetellaavium like other Bordetellae is a gram negative coccobacillus. [12] This genus is characterized by small aerobic bacteria (with the exception of B. petrii which is an anaerobe) that are oxidase and catalase positive and nitrate reduction and urease negative. [13] Bordetellae species produce two conserved toxins with a variety of additional toxins, individual to each species. [14] Unlike other Bordetellae, B. avium is motile and can grow in a filamentous form when grown in nutrient rich broth. [6] Pathogenic strains grow readily on a variety of media including chocolate and trypticase soy agar, [13] but MacConkey agar is recommended to differentiate this non fermentative bacterium from other fermentative species. [8] Whereas passage attenuated colonies typically have a roughened surface; [6] Pathogenic B. avium produces pearlescent colonies of 200-1000μm in diameter. [6] When grown on MacConkey agar, pathogenic isolates often develop a darkened raised center. [8]

Epidemiology

Turkey farming is a large industry with nearly 165 million kilograms of turkey products produced in Canada alone in 2019 [15] . In the Turkey Health Survey released annually by the United States Animal Health Association B. avium has ranked between 5th and 8th over the past 5 years making it a remarkable issue for production health management [16] .

Bordetella avium has a worldwide distribution but is found at the highest density in the North Temperate Zone, between the arctic circle and the Tropic of Cancer where the climate is most conducive to transfer. [6] Seasonality of outbreaks are most often recorded during the summer and fall months. [7] Outbreaks have been recorded in many countries including the United States, Canada, Australia, Germany, France, and South Africa. [7] When infections do occur nearly all of the flock becomes affected leading to a high reported morbidity with low mortality. [8] [9] Severity of disease can be exacerbated by adverse environmental conditions (low temperature, high ammonia and dust, low humidity) and secondary bacterial infections; increasing mortality up to 40% or 60%. [6] [8] It is uncommon to see outbreaks in breeder flocks, but up to 20% morbidity with no mortality is reported. [6] Furthermore, the bacterium is highly contagious and transmissible and the prevalence in bird species is abundant. [8] [9] Small backyard turkey flocks a mile from large commercial farms have shown isolated infections of B. avium. [6] B. avium is not able to transmit via vertical transmission, but it can transmit by direct contact between birds and remain in the environment in litter, food, and water for as long as 6 months. [6] [8] [17] B. avium also has a short incubation of only 7–10 days allowing for easy and rapid transmission. [6] [8] [18]

Although birds of all ages are susceptible, prevalence is highest and most well understood in domesticated turkeys, especially in the younger populations consisting of birds 1–6 weeks old. [6] [7] It is thought that birds who reach 5–6 weeks of age become relatively resistant to the clinical disease bordetellosis, yet, they can remain carriers among the flock. [8] In addition, much of the transmission is thought to relate to management practices and outbreaks are often associated with farms having confined spaces and flocks consisting of animals of varying ages. [6] [7] It is recommend that to limit disease transmission turkey farmers avoid multi-age flocks. [7]

Although less common, B. avium can also transmit to chickens as an opportunistic infection, and wildlife species where prevalence is still being evaluated. [18] It has been suggested that wildlife species act mainly as a reservoir and it is unclear if B. avium acts as part of the normal flora in wild bird populations or is a causative agent of disease. [18] [19] Despite the fact that wild birds are commonly asymptomatic, Bordetellosis has been reported in a variety of wild birds including parrot finches, partridges, cockatiels, and ostriches, among others. [18] In a study by Raffel et.al, in a sample of 46 Canada geese, 67% tested positive for B. avium using a serum agglutination test for antibodies. [18]

Beyond what is discussed here, many other studies have begun to look at characterizing the epidemiology of this bacterium. There is a strong interest in understanding the prevalence in different countries and prevalence among different species of domestic and wild birds. Understanding the epidemiology of this bacterium is of great importance to turkey producers as it remains one of the top 10 issues in domesticated turkeys. [16] Unfortunately, as research stands, the full epidemiological understanding of this bacterium remains to be fully understood.

Virulence Factors

B. avium exhibits its pathogenesis by attaching to the cilia on the respiratory epithelium of its host where it releases a number of cytotoxins capable of causing damage to the tracheal cartilage and associated structures. [8] [18] [17] Components enabling its attachment include pili, filamentous hemagglutinin, fimbriae, protein autotransporters, outer membrane proteins such as pertactin, and other lipopolysaccharide structures. [7] [8] [18] [17] The genes encoding for many of these proteins, such as fhaB (filamentous hemagglutinin) and fimA (fimbriae), as well as genes responsible for regulating the expression of virulence factors, such as bvgA (Bordetella virulence gene), have been identified and detected on confirmed isolates of B. avium. [8]

Identified cytotoxins produced by B. avium include an osteotoxin, a tracheal cytotoxin, a non-proteolytic dermonecrotic toxin that has been associated with nasal turbinate atrophy in pigs, and adenylate cyclase hemolysin with antiphagocytic activity. [7] [8] [17] The osteotoxin is known to be cytotoxic for osteogenic cells and rat osteosarcoma cells, in addition to embryonic tracheal cells and fetal bovine trabecular cells. [14] Its cytotoxic effect is achieved through the cleavage of L-cystine to form reactive sulfane-containing metabolites, which are then attached to proteins that are critical for the cell's survival. [14] Virulence also requires iron, which is acquired through the use of heme receptors, siderophore receptors, and transferrin-binding proteins. [8]

Clinical Significance

The typical host for Bordetella avium is the turkey. [6] In turkeys this bacteria primarily leads to inflammation of the respiratory mucosa; clinically this can present as sneezing, altered breathing, lower growth rate, vocalization changes, clear discharge from the eyes and nose, tracheal collapse, and submandibular edema. [6] [7] These clinical signs are typically evident within 7–10 days after infection. [8] In addition, their behaviour may change such that they are less active and will search out heat sources. [7] On necropsy turkeys commonly have softened tracheal rings, mucus in the trachea and sinuses dorsal to the tracheal bifurcation, and hemorrhage present on the tracheal lining. [8]

B. avium has also been isolated from other wild and domesticated birds including chickens, mallards, Canada geese, cockatiels, and ostriches. [18] It is uncertain if this bacterium causes disease in all these birds or if it is a part of their normal microbial flora. [18] Chickens have been shown to be affected, however, they are not as severely affected with Bordetellosis as turkeys are. [18] Most often this disease presents as severe respiratory disease in broilers, especially when they are concurrently infected with other respiratory viruses. [7] Cockatiels and ostriches also have been shown to develop the disease but it has not yet been studied to determine how the disease presents in these birds. [18]

As the severity of disease increases the most common comorbidity associated with Bordetella avium is a secondary infection with E. coli. [6] [8] B. avium is also thought to decrease an individual's ability to clear secondary organisms from the trachea which allows them to set up an infection. [6]

Zoonosis

B. avium is an opportunistic pathogen in humans and can cause respiratory disease, such as pneumonia, in immunocompromised patients. [7] [20] B. avium has also been isolated from human patients with cystic fibrosis (CF), however it is currently unclear if this bacteria is involved in the disease process of CF. [21] [20]

Control and Treatment

Environmental contamination is an important route of infection for B. avium. B. avium can survive in the environment less than 2 days at higher temperatures (40 °C), up to a month with low temperature (10 °C) and humidity (32-58%), and up to 6 months in feed, water and damp litter. [6] [8] Good bio-security protocols, thorough cleaning, and excellent husbandry practices are the best methods for controlling outbreaks. Optimal temperature, humidity, and control of ammonia and dust are critical to reduce B.avium growth in the environment and reduce irritants to the tracheal epithelium. [8] Most common disinfectants used do kill B. avium, and thorough cleaning includes removal of litter and other fomites between flocks, disinfection of the barn and flushing of water lines with disinfectants, and fumigation with methyl-bromide or formaldehyde. [6] Foot baths, using on farm-clothing, controlling traffic between barns, preventing contact with wild birds, and showers between sites also reduces transmission between farms. [6] [7] For infected flocks, increasing ventilation and reaching optimal temperature are key. [7] It has been reported that niacin or 0.016% oxy-halogen added to water lines given early in life reduces the severity of bordetellosis. [6] [8]

Antibiotic treatment is not considered effective for B. avium infections, as there is conflicting evidence for susceptibility; and most turkey poults with B.avium infection without secondary complications will recover from bordetellosis in 4–6 weeks, with resistance formed at 5–6 weeks. [6] [7] [8] [10] [11] The mechanism of bacterial resistance in some strains of B. avium have been recorded: there are resistance genes encoded on plasmids (pRAM resistance genes to tetracycline and 2 sulfonamides) and lack of a penicillin binding protein 3 (PBP3) which drugs bind to, to inhibit cell wall synthesis. Plasmid conjugation between B. avium isolates also occurs. [10] Most isolate strains of B. avium have resistance to a number of antibiotics. Resistance has been elucidated to aztreonam, ampicillin, tetracycline, cephalosporins, penicillins, sulbactam, sulfonamides, streptomycin, carbapenem, imipenem, fluoroquinolones, chloramphenicol, gentamicin, cefoperazone, cefepime, ceftazidime, piperacillin and amikacin. [6] [10]  However, some susceptibility has also been shown to ampicillin, amoxicillin, penicillin, ceftiofur, enrofloxacin, norfloxacin, ciprofloxacin, erythromycin, florfenicol, and co-trimoxazole. [11] The difficulty with characterizing antibiotic resistance and susceptibility in B. avium strains is most strains will appear sensitive in vitro, but in reality has a much different outcome in vivo . [6] Isolates are believed to be sensitive in vitro but not in vivo due to the inability of the drug to reach therapeutic doses within the tracheal epithelium of turkeys where bacteria dwell. [7] [8]

Two vaccines are available for poultry against B. avium bordetellosis: a temperature sensitive mutant live strain of B.avium and a bacterin isolate vaccine. [7] Bacterins are administered to breeder hens to induce maternal IgG to pass onto their progeny, providing maternal immunity up to 4 weeks in poults. The mutant live-strain is administered to poults twice; at hatchery and then at 2–3 weeks of age. [6] [7] However, vaccines are not known to be very efficacious, and may only protect against severe clinical signs, or delay onset of disease, not stop the spread of infection. Most significant immunity in turkey poults is thought to be acquired humoral immunity at this time. [6] [8] Vaccinations are considered for prevention if there is recurrence in outbreaks of bordetellosis. [17]

Related Research Articles

<i>Staphylococcus aureus</i> Species of Gram-positive bacterium

Staphylococcus aureus is a gram-positive spherically shaped bacterium, a member of the Bacillota, and is a usual member of the microbiota of the body, frequently found in the upper respiratory tract and on the skin. It is often positive for catalase and nitrate reduction and is a facultative anaerobe, meaning that it can grow without oxygen. Although S. aureus usually acts as a commensal of the human microbiota, it can also become an opportunistic pathogen, being a common cause of skin infections including abscesses, respiratory infections such as sinusitis, and food poisoning. Pathogenic strains often promote infections by producing virulence factors such as potent protein toxins, and the expression of a cell-surface protein that binds and inactivates antibodies. S. aureus is one of the leading pathogens for deaths associated with antimicrobial resistance and the emergence of antibiotic-resistant strains, such as methicillin-resistant S. aureus (MRSA). The bacterium is a worldwide problem in clinical medicine. Despite much research and development, no vaccine for S. aureus has been approved.

<i>Streptococcus pneumoniae</i> Species of bacterium

Streptococcus pneumoniae, or pneumococcus, is a Gram-positive, spherical bacteria, alpha-hemolytic member of the genus Streptococcus. S. pneumoniae cells are usually found in pairs (diplococci) and do not form spores and are non motile. As a significant human pathogenic bacterium S. pneumoniae was recognized as a major cause of pneumonia in the late 19th century, and is the subject of many humoral immunity studies.

<i>Campylobacter jejuni</i> Species of bacterium

Campylobacter jejuni is a species of pathogenic bacteria that is commonly associated with poultry, and is also often found in animal feces. This species of microbe is one of the most common causes of food poisoning in Europe and in the US, with the vast majority of cases occurring as isolated events rather than mass outbreaks. Active surveillance through the Foodborne Diseases Active Surveillance Network (FoodNet) indicates that about 20 cases are diagnosed each year for each 100,000 people in the US, while many more cases are undiagnosed or unreported; the CDC estimates a total of 1.5 million infections every year. The European Food Safety Authority reported 246,571 cases in 2018, and estimated approximately nine million cases of human campylobacteriosis per year in the European Union. Campylobacter jejuni infections are increasing at an alarming rate in Europe, North America, and Australia. In Africa, Asia, and the Middle East, data indicates that C. jejuni infections are endemic.

<i>Erysipelothrix rhusiopathiae</i> Species of pathogenic bacterium

Erysipelothrix rhusiopathiae is a Gram-positive, catalase-negative, rod-shaped, non-spore-forming, nonacid-fast, nonmotile bacterium. Distributed worldwide, E. rhusiopathiae is primarily considered an animal pathogen, causing the disease known as erysipelas that may affect a wide range of animals. Pigs, turkeys and laying hens are most commonly affected, but cases have been reported in other mammals, birds, fish, and reptiles. In pigs, the disease is known as diamond skin disease. The bacterium can also cause zoonotic infections in humans, called erysipeloid. The human disease called erysipelas is not caused by E. rhusiopathiae, but by various members of the genus Streptococcus.

<i>Haemophilus influenzae</i> Species of bacterium

Haemophilus influenzae is a Gram-negative, non-motile, coccobacillary, facultatively anaerobic, capnophilic pathogenic bacterium of the family Pasteurellaceae. The bacteria are mesophilic and grow best at temperatures between 35 and 37 °C.

<i>Bordetella</i> Genus of bacteria

Bordetella is a genus of small, Gram-negative, coccobacilli bacteria of the phylum Pseudomonadota. Bordetella species, with the exception of B. petrii, are obligate aerobes, as well as highly fastidious, or difficult to culture. All species can infect humans. The first three species to be described ; are sometimes referred to as the 'classical species'. Two of these are also motile.

<span class="mw-page-title-main">Infectious bursal disease</span> Viral disease of poultry

Infectious bursal disease (IBD), also known as Gumboro disease, infectious bursitis, and infectious avian nephrosis, is a highly contagious disease of young chickens and turkeys caused by infectious bursal disease virus (IBDV), characterized by immunosuppression and mortality generally at 3 to 6 weeks of age. The disease was first discovered in Gumboro, Delaware in 1962. It is economically important to the poultry industry worldwide due to increased susceptibility to other diseases and negative interference with effective vaccination. In recent years, very virulent strains of IBDV (vvIBDV), causing severe mortality in chicken, have emerged in Europe, Latin America, South-East Asia, Africa, and the Middle East. Infection is via the oro-fecal route, with affected birds excreting high levels of the virus for approximately 2 weeks after infection. The disease is easily spread from infected chickens to healthy chickens through food, water, and physical contact.

Avian coronavirus is a species of virus from the genus Gammacoronavirus that infects birds; since 2018, all gammacoronaviruses which infect birds have been classified as this single species. The strain of avian coronavirus previously known as infectious bronchitis virus (IBV) is the only coronavirus that infects chickens. It causes avian infectious bronchitis, a highly infectious disease that affects the respiratory tract, gut, kidney and reproductive system. IBV affects the performance of both meat-producing and egg-producing chickens and is responsible for substantial economic loss within the poultry industry. The strain of avian coronavirus previously classified as Turkey coronavirus causes gastrointestinal disease in turkeys.

<i>Chlamydia psittaci</i> Species of bacterium

Chlamydia psittaci is a lethal intracellular bacterial species that may cause endemic avian chlamydiosis, epizootic outbreaks in other mammals, and respiratory psittacosis in humans. Potential hosts include feral birds and domesticated poultry, as well as cattle, pigs, sheep, and horses. C. psittaci is transmitted by inhalation, contact, or ingestion among birds and to mammals. Psittacosis in birds and in humans often starts with flu-like symptoms and becomes a life-threatening pneumonia. Many strains remain quiescent in birds until activated by stress. Birds are excellent, highly mobile vectors for the distribution of chlamydia infection, because they feed on, and have access to, the detritus of infected animals of all sorts.

<i>Bordetella pertussis</i> Species of bacterium causing pertussis or whooping cough

Bordetella pertussis is a Gram-negative, aerobic, pathogenic, encapsulated coccobacillus bacterium of the genus Bordetella, and the causative agent of pertussis or whooping cough. Its virulence factors include pertussis toxin, adenylate cyclase toxin, filamentous hæmagglutinin, pertactin, fimbria, and tracheal cytotoxin.

<span class="mw-page-title-main">Gapeworm</span> Species of roundworm

A gapeworm, also known as a red worm and forked worm, is a parasitic nematode worm that infects the tracheas of certain birds. The resulting disease, known as "gape", occurs when the worms clog and obstruct the airway. The worms are also known as "red worms" or "forked worms" due to their red color and the permanent procreative conjunction of males and females. Gapeworms are common in young, domesticated chickens and turkeys.

<i>Pasteurella multocida</i> Species of bacterium

Pasteurella multocida is a Gram-negative, nonmotile, penicillin-sensitive coccobacillus of the family Pasteurellaceae. Strains of the species are currently classified into five serogroups based on capsular composition and 16 somatic serovars (1–16). P. multocida is the cause of a range of diseases in mammals and birds, including fowl cholera in poultry, atrophic rhinitis in pigs, and bovine hemorrhagic septicemia in cattle and buffalo. It can also cause a zoonotic infection in humans, which typically is a result of bites or scratches from domestic pets. Many mammals and birds harbor it as part of their normal respiratory microbiota.

Dichelobacter nodosus, formerly Bacteroides nodosus, is a Gram-negative, obligate anaerobe of the family Cardiobacteriaceae. It has polar fimbriae and is the causative agent of ovine foot rot as well as interdigital dermatitis. It is the lone species in the genus Dichelobacter.

<i>Mycoplasma gallisepticum</i> Species of bacterium

Mycoplasma gallisepticum (MG) is a bacterium in the class Mollicutes and the family Mycoplasmataceae. It causes chronic respiratory disease (CRD) in chickens and infectious sinusitis in turkeys, chickens, game birds, pigeons, and passerine birds of all ages. Mycoplasma gallisepticum is a significant pathogen in poultry.

<span class="mw-page-title-main">Fowl cholera</span> Bacterial disease of birds

Fowl cholera is also called avian cholera, avian pasteurellosis and avian hemorrhagic septicemia.

Brachyspira pilosicoli is a gram-negative, anaerobic, host-associated spirochete that colonizes the intestinal tract of animals and humans. It appears as a characteristic "false brush border" due to its end-on attachment to enterocytes of the colon where it interferes with intestinal absorption. B. pilosicoli is unique from other Brachyspira species because it colonizes a variety of domestic animals including pigs, chickens, dogs, wild birds, rodents, and humans. It is the causative agent of intestinal spirochetosis in pigs, chickens, and humans. In particular, B. pilosicoli has been described as an important colonic pathogen of pigs and chickens, causing colitis and diarrhea resulting in depressed rates of growth and impaired production on farms where infections with B. pilosicoli may be endemic. Bacterial attachment disrupts the colonic enterocytes and associated villi, causing the symptoms characteristic of intestinal spirochetosis. Additionally, B. pilosicoli is associated with clinical disease in human infections where it has implications for public health.

Staphylococcus pseudintermedius is a gram-positive spherically shaped bacterium of the genus Staphylococcus found worldwide. It is primarily a pathogen for domestic animals, but has been known to affect humans as well. S. pseudintermedius is an opportunistic pathogen that secretes immune-modulating virulence factors, has many adhesion factors, and the potential to create biofilms, all of which help to determine the pathogenicity of the bacterium. Diagnoses of S. pseudintermedius have traditionally been made using cytology, plating, and biochemical tests. More recently, molecular technologies like MALDI-TOF, DNA hybridization and PCR have become preferred over biochemical tests for their more rapid and accurate identifications. This includes the identification and diagnosis of antibiotic resistant strains.

<i>Avian metaavulavirus 2</i> Species of virus

Avian metaavulavirus 2, formerly Avian paramyxovirus 2, is a species of virus belonging to the family Paramyxoviridae and genus Metaavulavirus. The virus is a negative strand RNA virus containing a monopartite genome. Avian metaavulavirus 2 is one of nine species belonging to the genus Metaavulavirus. The most common serotype of Avulavirinae is serotype 1, the cause of Newcastle disease (ND). Avian metaavulavirus 2 has been known to cause disease, specifically mild respiratory infections in domestic poultry, including turkeys and chickens, and has many economic effects on egg production and poultry industries. The virus was first isolated from a strain in Yucaipa, California in 1956. Since then, other isolates of the virus have been isolated worldwide.

Histophilus somni is a non-motile, gram-negative, rod or coccobacillus shaped, facultative anaerobe bacterial species belonging to the family Pasteurellaceae. Prior to 2003, it was thought Haemophilus somnus, Histophilus ovis, and Histophilus agni were three different species, but now are all classified as Histophilus somni. Histophilus somni is a commensal bacteria of mucous membranes of the upper respiratory tract and reproductive tract with a global prevalence and is found in cattle and other small ruminants. Histophilus somni is also a known causative agent that is a part of the Bovine Respiratory Disease (BRD) complex, which typically involves multiple pathogens residing together in biofilm environments. Histophilus somni may also cause Histophilosus symptoms and clinical presentation will depend on the tissue affected. When disease does occur, it can be difficult to catch in time and is often diagnosed post mortem. This means that treatment often involves metaphylactic mass treatment or no treatment at all. This organism is more fastidious than others and requires knowledge for sample collection, storage and culture. Genomic studies related to this bacteria have enabled scientists to pinpoint antibiotic resistance genes.  

<span class="mw-page-title-main">Airsacculitis</span> Bacterial, fungal or viral inflammatory disease of air sacs in birds.

Airsacculitis, also known as air sacculitis, aerosacculitis, air sac disease, air sac infection, air sac syndrome and simply sac disease, is a common inflammatory condition of air sacs that occurs in birds and is caused by various microbial taxa. Having multiple different causative agents, the condition is widely distributed around the world.

References

  1. LPSN bacterio.net Archived September 22, 2013, at the Wayback Machine
  2. "Straininfo of Bordetella avium". Archived from the original on 2019-01-17. Retrieved 2013-07-25.
  3. Emerging infectious diseases
  4. Zoologix
  5. BioCyn Database Collection
  6. 1 2 3 4 5 6 7 8 9 10 11 12 13 14 15 16 17 18 19 20 21 22 23 24 25 26 Jackwood, Mark. W.; Saif, Y. M. (2008). "Section II Bacterial Diseases: Bordetellosis (Turkey Coryza". Diseases of poultry (12 ed.). Ames, IA: Blackwell Pub. pp. 774–784.
  7. 1 2 3 4 5 6 7 8 9 10 11 12 13 14 15 16 17 18 19 Brash, M.L.; Charlton, B.R.; Fitz-Coy, S.H.; Fulton, R.M.; Julian, R.J.; Jackwood, M.W.; Ojkic, D; Newman, L. J.; Sander, J. E. (2013). Boulianne, M (ed.). "Avian Disease Manual". aaap.memberclicks.net (7th ed.). Jacksonville, FL. Retrieved 2020-09-20.
  8. 1 2 3 4 5 6 7 8 9 10 11 12 13 14 15 16 17 18 19 20 21 22 23 24 Register, Karen (March 2020). "Bordetellosis in Poultry - Poultry". Merck Veterinary Manual. Retrieved 2020-09-18.
  9. 1 2 3 Śmiałek, M.; Tykałowski, B.; Pestka, D.; Stenzel, T.; Koncicki, A. (2015-09-01). "Epidemiological situation of turkey coryza (bordetellosis) in Poland". Polish Journal of Veterinary Sciences. 18 (3): 659–661. doi: 10.1515/pjvs-2015-0085 . ISSN   2300-2557. PMID   26618601.
  10. 1 2 3 4 Beach, Nathan M.; Thompson, Seth; Mutnick, Rachel; Brown, Lisa; Kettig, Gina; Puffenbarger, Robyn; Stockwell, Stephanie B.; Miyamoto, David; Temple, Louise (November 2012). "Bordetella avium antibiotic resistance, novel enrichment culture, and antigenic characterization". Veterinary Microbiology. 160 (1–2): 189–196. doi:10.1016/j.vetmic.2012.05.026. PMC   3469198 . PMID   22721730.
  11. 1 2 3 Nhung, Nguyen Thi; Chansiripornchai, Niwat; Carrique-Mas, Juan J. (2017-08-10). "Antimicrobial Resistance in Bacterial Poultry Pathogens: A Review". Frontiers in Veterinary Science. 4: 126. doi: 10.3389/fvets.2017.00126 . ISSN   2297-1769. PMC   5554362 . PMID   28848739.
  12. Finger, Horst; von Koenig, Carl Heinz Wirsing (1996), Baron, Samuel (ed.), "Bordetella", Medical Microbiology (4th ed.), Galveston (TX): University of Texas Medical Branch at Galveston, ISBN   978-0-9631172-1-2, PMID 21413270, retrieved 2020-09-21
  13. 1 2 Harrington A., Castelanos J., Ziedalski T., Clarridge J., and Cookson B. Isolation of Bordetella avium and Novel Bordetella Strain from Patients with Respiratory Disease. Emerg Infect Dis. 2009 Jan; 15(1): 72–74. doi: 10.3201/eid1501.071677
  14. 1 2 3 Gentry-Weeks, C., Keith, J. M., & Thompson, J. (1993). Toxicity of Bordetella auium @-Cystathionase toward MC3T3-E 1 Osteogenic Cells*. THE JOURNAL OF BIOLOGICAL CHEMISTRY (Vol. 268).
  15. "Industry Facts & Stats – Turkey Farmers of Canada". www.turkeyfarmersofcanada.ca. Retrieved 2020-10-25.
  16. 1 2 "United States Animal Health Association". www.usaha.org. Retrieved 2020-10-25.
  17. 1 2 3 4 5 Quinn, P. J. (27 July 2015). Concise review of veterinary microbiology. Markey, B. K. (Bryan K.), Leonard, F. C., FitzPatrick, E. S., Fanning, S. (Second ed.). Chicheser, West Sussex, UK. ISBN   978-1-118-80269-4. OCLC   915155688.{{cite book}}: CS1 maint: location missing publisher (link)
  18. 1 2 3 4 5 6 7 8 9 10 11 Raffel, Thomas R.; Register, Karen B.; Marks, Stephen A.; Temple, Louise (September 19, 2020). "Prevalence of Bordetella avium Infection in Selected Wild and Domesticated Birds in the Eastern USA". Journal of Wildlife Diseases. 38 (1): 40–46. doi: 10.7589/0090-3558-38.1.40 . ISSN   0090-3558. PMID   11838227. S2CID   2918206.
  19. Eldin, Walaa Fathy Saad; Abd-El Samie, Lammah K.; Darwish, Wageh Sobhy; Elewa, Yaser Hosny A. (2019-08-02). "Prevalence, virulence attributes, and antibiogram of Bordetella avium isolated from turkeys in Egypt". Tropical Animal Health and Production. 52 (1): 397–405. doi:10.1007/s11250-019-02027-5. ISSN   0049-4747. PMID   31376060. S2CID   199388030.
  20. 1 2 Harrington, Amanda T.; Castellanos, Jaime A.; Ziedalski, Tomasz M.; Clarridge, Jill E.; Cookson, Brad T. (2009). "Isolation of Bordetella avium and Novel Bordetella Strain from Patients with Respiratory Disease - Volume 15, Number 1—January 2009 - Emerging Infectious Diseases journal - CDC". Emerging Infectious Diseases. 15 (1): 72–4. doi:10.3201/eid1501.071677. PMC   2660683 . PMID   19116056.
  21. Spilker, T.; Liwienski, A.A.; LiPuma, J.J. (2008-05). "Identification of Bordetella spp. in respiratory specimens from individuals with cystic fibrosis". Clinical Microbiology and Infection. 14 (5): 504–506. doi:10.1111/j.1469-0691.2008.01968.x. ISSN  1198-743X.