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Query: UMLS:C0040584 (tracheitis)
 384 document(s) hit in 31,850,051 MEDLINE articles (0.00 seconds)

Two cases of respiratory disease in pigeons are described. The first case involved pneumonia and tracheitis, and the second case involved tracheitis. In both cases, unusual gram-negative, non-fermenting, short rod-shaped bacteria were recovered along with other microorganisms. The bacteria produced small, glistening, gray colonies on blood agar, did not grow on MacConkey agar, were unreactive on several biochemical tests, and resembled Pasteurella anatipestifer. Neither pigeon isolate was distinguished from P. anatipestifer by biochemical tests. However, there were morphologic and growth differences between the pigeon isolates and P. anatipestifer. Furthermore, unlike P. anatipestifer, both pigeon isolates were sensitive to aminoglycoside antibiotics and to polymyxin B. Finally, neither isolate was agglutinated by antisera to 15 serotypes of P. anatipestifer. Diagnosticians, especially those who seldom encounter P. anatipestifer, might have difficulty distinguishing the pigeon isolates from P. anatipestifer because of their close resemblance.
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PMID:Pasteurella anatipestifer-like bacteria associated with respiratory disease in pigeons. 825 93

Under an influenza surveillance initiated in Pune, India, 2 or 3 dispensaries and small hospitals where patients with acute respiratory disease (ARD) sought medical assistance were chosen for regular weekly visits to collect a sufficient number of specimens. A case of ARD included individuals with the following conditions: common cold, pharyngitis, laryngitis, tracheitis, bronchitis, bronchiolitis, pneumonia, or bronchopneumonia. During the period of surveillance of 1978-90, more than 10,000 cases of ARD among various age groups were investigated. The majority of cases were in children and infants. Most of the patients were seen during investigations of 16 outbreaks of influenza. Generally, the cases presented with 2 or 3 symptoms of respiratory disease and 1 or 2 systemic manifestations. Throat and nasal swabs were collected from ARD cases during the acute phase of their illness (1-4 days). Throat/nasal swabs were taken from over 10,000 ARD cases. About 80% of these specimens were cultivated for influenza virus in embryonated chicken eggs (9-11 days' old) and about 39% in Madin-Darby canine kidney cell culture (MDCK) with crystalline trypsin. Several variants of influenza virus types A and B were isolated during the 16 outbreaks including these variant strains: A/USSR/77 (H1N1) in 1978; A/Singapore/6/86 (H1N1) in 1986; and B/Yamagata/16/88-like in 1990. A total of 290 influenza virus isolates comprising several variants of influenza type A (H3N2) and A (H1N1) and type B were isolated. The variant strains of influenza type A (H1N1), type A (H3N2), and type B circulated regularly either every year or in alternate years. 181 of 290 of the influenza isolates were from children aged 10 years. Analysis of the isolates showed that 174 were from the rainy months of July, August, and September, and the maximum number of 93 occurred in July. Of the 16 outbreaks of influenza, 10 occurred in the rainy season, 3 in the hot season, 1 in the cool season, and 2 in February and March.
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PMID:Influenza surveillance in Pune, India, 1978-90. 849 Sep 80

An outbreak of conjunctivitis and severe respiratory disease occurred in an integrated chukar partridge (Alectoris graeca) operation that involved about 8000 birds. The main clinical features were conjunctivitis and sinusitis and frequent mouth breathing, but almost no gasping or coughing. In 1000 breeders, egg production declined from 73% to 20%. Morbidity reached 100%, and losses from mortality and culling approached 60%. At necropsy, a conjunctivitis (often bilateral) and extensive caseated sinusitis were common. There was an occasional slight mucoid tracheitis, but no significant air sac lesions were noted. Mycoplasma gallisepticum, designated strain GM1125, was isolated and identified. Exposure of susceptible chukars to GM1125 reproduced the field disease. GM1125 was reisolated from the conjunctiva of all exposed birds 12 days postinfection, but infrequently from there or the respiratory system 36 days postexposure, even though clinical disease was still present. The experimental disease was confined to the conjunctiva and the upper respiratory tract. An occasional mucoid tracheitis was noted, but generally, the lungs and air sacs were not involved. Infection was followed by an appreciable serological response to M. gallisepticum.
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PMID:Experimental reproduction of Mycoplasma gallisepticum disease in chukar partridges (Alectoris graeca). 879 Aug 93

A 60-year-old captive California desert tortoise (Gopherus agassizii) which died in August 1990 at the University of California, Davis, California (USA), during treatment for colonic impaction had marked caseous necrosis of the oral cavity, choana, trachea, and lungs. Numerous intranuclear inclusion bodies and a large number of syncytial giant cells were seen in the oral cavity and respiratory tract along with bacterial granulomas. Pasteurella testudinis, Streptococcus veridans, and coagulase-negative Staphilococcus spp. were cultured from the lesions. Using electron microscopy, herpesvirus particles were observed in intranuclear inclusions and cytoplasm. Viral stomatitis, tracheitis, and bronchopneumonia complicated by bacterial infection were diagnosed. Although respiratory disease is common in desert tortoises, this is believed to be the first report of association with a viral infection.
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PMID:Herpesvirus particles associated with oral and respiratory lesions in a California desert tortoise (Gopherus agassizii). 882 80

Cryptosporidium baileyi causes respiratory disease in chickens. The purposes of this prospective study were to determine the incidence of C. baileyi tracheitis among broilers in a commercial setting, and the relationship between C. baileyi tracheitis and production performance parameters. All samples came from 56 farms that grow broilers for one company in northern Georgia. Tracheas were collected and examined with a light microscope and cultured for viruses and bacteria. Overall, 23 of 56 (41%) broiler flocks had C. baileyi tracheitis. Parasitism rates among C. baileyi-infected flocks ranged from a low of 10% to a high of 60%. Cryptosporidium baileyi tracheitis was very highly correlated (rho = 0.81, n = 56, P < 0.00001) to severity of tracheitis, negatively correlated (rho = -0.27, n = 56, P < 0.04) with average body weight, and correlated with airsacculitis (rho = 0.30, n = 56, P < 0.03) and condemnations (rho = 0.27, n = 56, P < 0.05). The present study indicates that C. baileyi infection rates are high, and the role that this parasite plays in the pathogenesis of respiratory disease and production losses could be unexpectedly large.
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PMID:Respiratory coccidiosis (Cryptosporidium baileyi) among northern Georgia broilers in one company. 888 86

A free-living adult male gopher tortoise (Gopherus polyphemus) was found on Sanibel Island, Florida (USA), on 18 February 1992 with signs of upper respiratory disease. On necropsy after euthanasia on 27 February 1992, severe, extensive necrotizing ulcerative tracheitis, multifocal necrotizing pneumonia, and multifocal necrotizing ulcerative pharyngitis and esophagitis were observed. Large ovoid to round intracytoplasmic basophilic inclusions, which appeared to displace the nucleus to the cell periphery, occurred within degenerate and necrotic epithelial cells of the above tissues. On transmission electron microscopy of formalin-fixed trachea and lung, intracytoplasmic viral particles were observed within necrotic cells in the tracheal lumen and epithelial cells of the lung. Most infected cells also had a roughly spherical granular cytoplasmic inclusion that contained clusters of viral particles. Viral particles had an electron dense spherical to icosahedral core surrounded by a less electron dense icosahedral capsid. Mature extracellular virions were surrounded by an envelope and were 150 to 220 nm in diameter. Virions and cytoplasmic inclusions were morphologically similar to those of the Family Iridoviridae.
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PMID:Respiratory and pharyngo-esophageal iridovirus infection in a gopher tortoise (Gopherus polyphemus). 935 71

Proliferative lymphocytic tracheitis and pneumonia were observed histologically in the respiratory tract of a captive Burmese python (Python molurus bivittatus). A mycoplasma species was isolated from the respiratory tissue. Polymerase chain reaction analysis of the 16S rRNA gene sequence of the isolate showed 0.90 similarity to Mycoplasma agassizii, an organism previously shown to cause respiratory disease in reptiles. Based on these findings, a novel Mycoplasma species was suspected to be the causative agent of respiratory disease in this snake.
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PMID:A novel Mycoplasma sp. associated with proliferative tracheitis and pneumonia in a Burmese python (Python molurus bivittatus). 944 90

An avian pneumovirus (APV) was isolated from commercial turkeys in Colorado (APV/Colorado) showing clinical signs of a respiratory disease. The results of virus neutralization and indirect fluorescent antibody tests showed that the APV/Colorado was partially related to APV subgroup A but was unrelated to APV subgroup B. Turkeys experimentally inoculated with the APV/Colorado were observed for signs, lesions, seroconversion, and virus shedding. Thirty-six 7-wk-old turkeys were distributed into three groups. Eighteen turkeys were inoculated oculonasally with APV/Colorado, six were placed in contact at 1 day postinoculation (DPI), and 12 served as noninoculated controls. Tracheal swabs and blood samples were collected at 3, 5, 7, 10, 14, and 21 DPI. Tissues were collected from three inoculated and two control turkeys on aforementioned days for pathologic examination and APV isolation. Inoculated turkeys developed respiratory disease, yielded APV at 3, 5, and 7 DPI, and seroconverted at 10 DPI. Contact turkeys yielded APV at 7 and 10 DPI. No gross lesions were observed in the turbinates, infraorbital sinuses, and trachea. However, microscopic examination revealed acute rhinitis, sinusitis, and tracheitis manifested by congestion, edema, lymphocytic and heterophilic infiltration, and loss of ciliated epithelia. The inflammatory lesions were seen at 3 DPI and became extensive at 5 and 7 DPI. Active regenerative changes in the epithelia were seen at 10 and 14 DPI. Serologic survey for the presence of antibodies in commercial turkeys (24,504 sera from 18 states) and chickens (3,517 sera from 12 states) to APV/Colorado showed seropositive turkeys in Minnesota, North Dakota, and South Dakota and no seropositive chickens. This report is the first on the isolation of an APV and APV infection in the United States.
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PMID:Experimental and serologic observations on avian pneumovirus (APV/turkey/Colorado/97) infection in turkeys. 1073 40

Acute infections of the respiratory tract are common in pediatric patients. Respiratory disease is the leading cause of hospitalization in children less than 4 years of age and is responsible for many physicians' office and emergency department visits.(1) The severity of upper respiratory tract infection ranges from mild, self-limited disease to potentially life-threatening airway obstruction. The prepared clinician can often make a diagnosis based solely on the history and physical examination, using radiographs and laboratory examinations to aid in diagnosis when the clinical picture is unclear. At times, airway collapse is imminent, and the clinician must proceed directly to endoscopy for definitive diagnosis and airway protection. This article will discuss the pathogenesis, clinical presentation, and management of epiglottitis, croup, and bacterial tracheitis in the pediatric population.
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PMID:An update on inflammatory disorders of the pediatric airway: epiglottitis, croup, and tracheitis. 1146 24

Infectious laryngotracheitis virus (ILTV) is routinely diagnosed by histopathologic examination of trachea, eyelid, and lung tissues. Lesions consistent with infectious laryngotracheitis (ILT) infection include syncytial cell formation with intranuclear inclusion bodies. These changes are present during the acute phase of infection. To increase the sensitivity of detecting ILT, a nested polymerase chain reaction (PCR) was developed for detection of ILTV DNA. Nested PCR assay was specific for the amplification of ILTV DNA and did not amplify a variety of other avian pathogens. To further validate the ability of this assay to detect ILT, nested PCR was performed in formalin-fixed, paraffin-embedded tissues from 35 cases of respiratory disease. Of the 35 cases, 12 were considered ILT suspects on the basis of initial clinical observation. Eleven of the 12 ILT-suspect cases were diagnosed as ILT, and the remaining 24 were diagnosed as nonspecific tracheitis (NST) by histopathologic examination. Histopathologically positive samples were confirmed by direct fluorescent antibody test and virus isolation. Of the 11 ILT-positive cases, 10 were positive by nested PCR. In addition, ILTV DNA was detected in 7 of the 24 samples diagnosed as NST upon histopathologic examination. Therefore, by nested PCR, ILTV DNA was detected in tissues independently of the presence of syncytial cells, intranuclear inclusions, or both. ILT nested PCR is a specific and sensitive assay capable of detecting ILT at different stages of infection and can be utilized in combination with histopathological examination to accelerate the diagnosis of ILT infection.
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PMID:Detection of infectious laryngotracheitis virus in formalin-fixed, paraffin-embedded tissues by nested polymerase chain reaction. 1192 50


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