1). The same pattern existed among strains producing the other Vsa isotypes. Strains producing short Vsa proteins attached to MLE-12 cells in statistically significant higher numbers than did those strains that produced long proteins. These findings were true for strains producing a short or long VsaA protein, a short or long VsaI protein, and VsaH. There is no long form of the VsaH because this protein lacks tandem repeats (Simmons et al., 1996, 2004). There were no statistical differences observed between the Vsa isotypes examined. The only significant differences

were between strains producing short and long Vsa proteins. The mutants that lack EPS-I that APO866 manufacturer are available all produce a long VsaG protein. The EPS-I mutants CTG1291 and CTG1701 exhibited statistically significant reduced attachment to MLE-12 cells as compared to all strains CT99021 of mycoplasma that produced the polysaccharide (Fig. 2). The complemented mutant that had restored EPS-I production, strain CTG1701-C, attached as well as did the wild-type long VsaG-producing strain CTG38. The reduced attachment of the mutants is attributed to the loss of the EPS-I polysaccharide,

because the VsaG proteins produced by the mutant, wild-type, and complemented strains are indistinguishable by Western blot (Daubenspeck et al., 2009). As above, mycoplasmas producing a short VsaG exhibited statistically significant more adherence than did the strains that produced a long VsaG. Because the EPS-I mutants have an enhanced ability to form a biofilm on glass and plastic surfaces (Daubenspeck et al., 2009), the poor cytoadherence of the mutants was unexpected. Hence, hemadsorption was used as another approach to assess the adherence properties of the strains under study. Mycoplasma pulmonis colonies were scored according to the percent sRBC adsorbed (HA score). The results are shown in Table 1. The median HA scores of all strains expressing the VsaG isotype were 0, regardless of Vsa length. The median HA scores of CT182-R3, 4-Aminobutyrate aminotransferase producing a short VsaA protein,

and CT182-R40, producing a long VsaA, were 4 and 2, respectively. Similarly, the median HA scores of CTI-R4, short VsaI, and CTI-R40, long VsaI, were 4 and 2, respectively. The CT-H.8 median HA score was 4. Excluding the VsaG-producing strains, the median score of all the short Vsa-producing mycoplasmas was significantly greater than all the long Vsa-producing mycoplasmas (P = 0.0008). The HA assays for the CTG-R5 (n = 466), CTG38 (n = 509), CTG1291 (n = 472), CTG1701 (n = 603), and CTG1701-C (n = 524) were performed separately from the assays for CT182-R3 (n = 411), CT182-R40 (n = 641), CTI-R4 (n = 276), CTI-R40 (n = 437), and CT-H.8 (n = 385). Because the VsaG-producing strains did not hemadsorb regardless of whether EPS-I was produced, no conclusion could be reached as to a possible role of EPS-I in hemadsorption.