Mycoplasma gallisepticum in house finches (Carpodacus mexicanus) and other wild birds associated with poultry production facilities

• Published in: Avian diseases 2001-04, Vol.45 (2), p.321-329
• Main Authors: Luttrell, M.P, Stallknecht, D.E, Kleven, S.H, Kavanaugh, D.M, Corn, J.L, Fischer, J.R
• Format: Article
• Language: English
• Subjects: Agglutination Tests - veterinary; Animals; Animals, Wild; Antigens; Aviculture; Bird Diseases - epidemiology; Bird Diseases - microbiology; Bird Diseases - transmission; Birds; Chickens; diagnostic techniques; disease prevalence; farms; Finches; Fringillidae; Georgia - epidemiology; Infections; Mycoplasma; Mycoplasma - isolation & purification; Mycoplasma gallisepticum; Mycoplasma Infections - epidemiology; Mycoplasma Infections - transmission; Mycoplasma Infections - veterinary; Polymerase Chain Reaction - veterinary; Poultry; Poultry Diseases - microbiology; Poultry Diseases - transmission; poultry farms; Prevalence; Risk Factors; seasonal variation; Songbirds; Wild birds
• ISSN: 0005-2086; 1938-4351
• DOI: 10.2307/1592971

Since 1994, an epidemic of conjunctivitis caused by Mycoplasma gallisepticum (MG) has spread throughout the eastern population of house finches (Carpodacus mexicanus). The adaptation of MG to a free-flying avian species presents potential problems for the control of mycoplasmosis in commercial poultry. To evaluate risks associated with this emerging problem, a field survey was conducted to assess prevalence of MG infection in house finches and other passerine birds associated with poultry farms. Between November 1997 and March 1999, 1058 birds were captured by mist net or trap at 17 farms and at 10 feeder stations in northeast Georgia. Birds were bled and screened by serum plate agglutination (SPA) for antibodies to MG. Birds with negative or weak positive SPA results were released at capture sites, and those with strong positive SPA reactions were kept for further evaluation. Necropsies were performed on selected house finches and individuals of 11 other passerine species, and samples were collected for MG testing by culture, polymerase chain reaction (PCR), hemagglutination inhibition, and histopathology. Testing revealed 19.1% of 671 birds caught at farms and 11.6% of 387 birds caught at feeder sites were SPA positive for MG. Three house finches captured on farms were positive for MG by culture and PCR, whereas three from feeder sites were positive only by PCR. No MG isolates were made from tufted titmice (Baeolophus bicolor), but 40% were positive by PCR. Individuals from 10 additional species were SPA positive only. Results suggest that MG persists at low levels in house finches in northeast Georgia and that tufted titmice may be nonclinical carriers of MG or a related mycoplasma. Positive SPA reactions in other species may be caused by nonspecific reactions or contact exposure. Current biosecurity recommendations should be sufficient to minimize risks of transmission between wild and domestic birds.