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. 2007 Dec;51(4):829-33.
doi: 10.1637/7806-120106-REGR.1.

Sialidase activity in Mycoplasma synoviae

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Sialidase activity in Mycoplasma synoviae

Meghan May et al. Avian Dis. 2007 Dec.

Abstract

Eleven strains of the avian pathogen Mycoplasma synoviae were evaluated for the presence of sialidase activity with the use of the fluorogenic substrate 2'-(4-methylumbelliferyl)-alpha-D-N-acetylneuraminic acid and the sialidase inhibitor 2-deoxy-2,3- didehydro-N-acetylneuraminic acid. The kinetics of in vitro growth in modified Frey medium were also assessed for each strain. Five strains had been isolated from clinically symptomatic chickens, and strains WVU 1853T and K3344 have been demonstrated to be capable of reproducing disease in specific-pathogen-free chickens. All strains exhibited sialidase activity, although the amount varied 65-fold among strains (P < 0.0001) from 1.3 x 10(-7) to 2.0 x 10(-9) activity units per colony-forming unit. Strains originally isolated from clinically symptomatic birds had more (P < 0.05) sialidase activity than strains from asymptomatic birds. Strain WVU1853T exhibited the most sialidase activity (P < 0.0001) and grew to the highest culture density (P < 0.0001) among strains, but across strains, the rank correlation of growth rate with sialidase activity was not significant. Negligible activity was detected in conditioned culture supernatant fluid. This is the first report of sialidase activity in pathogenic strains of M. synoviae, which suggests a potential enzymatic basis for virulence of the organism.

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Figures

Figure 1
Figure 1. Growth of Mycoplasma synoviae
Stocks (left to right: K5016, K4907, FMT33, K5599, K5113, MS173, F10-2AS, FMT126, K3344, MS117, MS178, WVU1853T) were grown in modified Frey’s medium (MFM) at 37 °C in 5% v/v CO2 without agitation. Triplicate cultures were initially synchronized by dilution with MFM to 507 ± 21 colony-forming units (CFUs) per mL. Aliquots were withdrawn every 24 hr for 120 hr to measure culture density. Strains FMT126, K3344, and MS117 reached a higher (*** = P < 0.0001) density than all other strains by 48 hr, although the density of strain WVU1853T exceeded all other strains at 72, 96 and 120 hr.

References

    1. Bencina D, Narat M, Dovc P, Drobnic-Valic M, Habe F, Kleven SH. The characterization of Mycoplasma synoviae EF-Tu protein and proteins involved in hemadherence and their N-terminal amino acid sequences. FEMS Microbiol Lett. 1999;173:85–94. - PubMed
    1. Brown DR, Farley JM, Zacher LA, Carlton JM, Clippinger TL, Tully JG, Brown MB. Mycoplasma alligatoris sp. nov., from American alligators. Int J Syst Evol Microbiol. 2001;51:419–424. - PubMed
    1. Brown DR, Nogueira MF, Schoeb TR, Vliet KA, Bennett RA, Pye GW, Jacobson ER. Pathology of experimental mycoplasmosis in American alligators. J Wildl Dis. 2001;37:671–679. - PubMed
    1. Brown DR, Zacher LA, Farmerie WG. Spreading factors of Mycoplasma alligatoris, a flesh-eating mycoplasma. J Bacteriol. 2004;186:3922–3927. - PMC - PubMed
    1. Cerda RO, Giacoboni GI, Xavier JA, Sansalone PL, Landoni MF. In vitro antibiotic susceptibility of field isolates of Mycoplasma synoviae in Argentina. Avian Dis. 2002;46:215–218. - PubMed

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