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Antigen-Capture Enzyme-Linked Immunosorbent Assay for Specific Detection of Mycoplasma pneumoniae
Published on: February 24, 2023
Mycoplasmas and respiratory disease in pheasants and partridges
Abstract:
Pheasants and partridges with signs of upper respiratory disease were cultured for mycoplasmas and were also examined for Mycoplasma gallisepticum and Mycoplasma synoviae using commercial polymerase chain reaction (PCR) kits. Sixty-two incidents of disease were investigated in pheasants and 12 in partridges. M. gallisepticum was detected by culture in only four and three incidents in pheasants and partridges, respectively, but with PCR a further 15 M. gallisepticum-positive incidents were detected in pheasants and another five in partridges. Several fast-growing Mycoplasma species, in particular Mycoplasma glycophilum, Mycoplasma gallinaceum and Mycoplasma pullorum, were isolated frequently and were thought to be impeding the isolation of M. gallisepticum by outgrowing it. Samples yielding M. gallisepticum isolates contained significantly fewer "contaminating" species and were exclusively from specimens submitted as whole heads rather than as swabs or as cultures from other laboratories. M. synoviae was not isolated and was detected in only one specimen by PCR.
Insights
Polymerase chain reaction (PCR) testing significantly improved the detection of Mycoplasma gallisepticum in pheasants and partridges compared to traditional culture methods. Other Mycoplasma species may hinder M. gallisepticum isolation.
Area of Science:
- Avian Pathology
- Microbiology
- Veterinary Medicine
Background:
- Upper respiratory disease is a significant concern in farmed pheasants and partridges.
- Mycoplasma gallisepticum (MG) and Mycoplasma synoviae (MS) are key avian pathogens.
- Accurate diagnosis of mycoplasmosis is crucial for disease management.
Purpose of the Study:
- To compare the efficacy of culture and polymerase chain reaction (PCR) for detecting Mycoplasma gallisepticum and Mycoplasma synoviae in diseased pheasants and partridges.
- To identify other Mycoplasma species present in these birds and assess their potential impact on MG detection.
Main Methods:
- Disease incidents in pheasants and partridges were investigated using bacterial culture and commercial PCR kits for MG and MS.
- Isolates were identified, and the prevalence of MG and MS was compared between culture and PCR methods.
- The presence of other Mycoplasma species was noted, particularly in relation to MG isolation success.
Main Results:
- PCR detected significantly more Mycoplasma gallisepticum-positive incidents (15 in pheasants, 5 in partridges) than culture (4 in pheasants, 3 in partridges).
- Fast-growing Mycoplasma species, including Mycoplasma glycophilum, Mycoplasma gallinaceum, and Mycoplasma pullorum, were frequently isolated.
- Whole head specimens yielded more successful MG isolations and had fewer "contaminating" species compared to swabs or cultures from other labs.
- Mycoplasma synoviae was rarely detected, with only one positive PCR result.
Conclusions:
- PCR is a more sensitive method than culture for diagnosing Mycoplasma gallisepticum infections in pheasants and partridges.
- The presence of other Mycoplasma species may interfere with the isolation of M. gallisepticum.
- Specimen type (whole head) and laboratory handling may influence diagnostic success for M. gallisepticum.
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