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Volume 3, Number 3—September 1997

Dispatch

Molecular Epidemiologic Investigations of Mycoplasma gallisepticum Conjunctivitis in Songbirds by Random Amplified Polymorphic DNA Analyses

David H. Ley*, J. Edward Berkhoff*, and Sharon Levisohn†
Author affiliations: *College of Veterinary Medicine, North Carolina State University, Raleigh, North Carolina, USA; †Visiting Research Scientist, Kimron Veterinary Institute, Bet Dagan, Israel

Main Article

Figure 4

RAPD (method II) patterns of MG vaccine strains (lanes 1-2) and isolates from house finches (lanes 4-11), and M. imitans type strain (lane 3). DNA base pair size standards are shown on the left. Lane 1 = ts-11; lane 2 = 6/85; lane 3 = M. imitans; lane 4 = K3839; lane 5 = K4013; lane 6 = K4013; lane 7 = K4117; lane 8 = 7994; lane 9 = 1652442; lane 10 = K4058; lane 11 = K4269. An additional RAPD primer set (method II) was used to determine whether method I accurately determined MG strain identitie

Figure 4. RAPD (method II) patterns of MG vaccine strains (lanes 1-2) and isolates from house finches (lanes 4-11), and M. imitans type strain (lane 3). DNA base pair size standards are shown on the left. Lane 1 = ts-11; lane 2 = 6/85; lane 3 = M. imitans; lane 4 = K3839; lane 5 = K4013; lane 6 = K4013; lane 7 = K4117; lane 8 = 7994; lane 9 = 1652442; lane 10 = K4058; lane 11 = K4269. An additional RAPD primer set (method II) was used to determine whether method I accurately determined MG strain identities.

Main Article

The conclusions, findings, and opinions expressed by authors contributing to this journal do not necessarily reflect the official position of the U.S. Department of Health and Human Services, the Public Health Service, the Centers for Disease Control and Prevention, or the authors' affiliated institutions. Use of trade names is for identification only and does not imply endorsement by any of the groups named above.

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