Research Topics
Species | KEVIN F DYBVIGSummaryAffiliation: University of Alabama at Birmingham Country: USA Publications
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Publications
A family of phase-variable restriction enzymes with differing specificities generated by high-frequency gene rearrangementsK Dybvig
Department of Comparative Medicine, University of Alabama at Birmingham, Birmingham, AL 35294 0019, USA
Proc Natl Acad Sci U S A 95:13923-8. 1998..These data cast doubt on the prevailing paradigms that restriction systems are either selfish or function to confer protection from invasion by foreign DNA...
Fewer essential genes in mycoplasmas than previous studies suggestKevin Dybvig
Department of Genetics, University of Alabama at Birmingham, Birmingham, AL, USA
FEMS Microbiol Lett 311:51-5. 2010..This study also revealed evidence of gene duplications in M. pulmonis and identified chromosome segregation proteins that are dispensable in mycoplasmas but essential in Bacillus subtilis...
Genome of Mycoplasma arthritidisKevin Dybvig
Department of Genetics, University of Alabama Birmingham, Birmingham, Alabama 35294 0024, USA
Infect Immun 76:4000-8. 2008..Of the 635 predicted coding regions, 218 were disrupted in a library of 1,100 members. Dispensable genes included the gene coding for the MAM superantigen and genes coding for ribosomal proteins S15, S18, and L15...
Evidence for type III restriction and modification systems in Mycoplasma pulmonisKevin Dybvig
Department of Genetics, 720 S 20th St, KAUL 720, University of Alabama at Birmingham, Birmingham, AL 35294 0024, USA
J Bacteriol 189:2197-202. 2007..Genomic data indicate that the cassette was acquired by horizontal gene transfer and possibly located on a mobile element...
The Vsa shield of Mycoplasma pulmonis is antiphagocyticBrandon M Shaw
Department of Genetics, University of Alabama at Birmingham, Birmingham, Alabama, USA
Infect Immun 80:704-9. 2012..These results may be pertinent to understanding the functions of similar proteins that have extensive repeat regions in other microbes...
Construction and use of derivatives of transposon Tn4001 that function in Mycoplasma pulmonis and Mycoplasma arthritidisK Dybvig
Department of Comparative Medicine, University of Alabama at Birmingham, Birmingham, Alabama 35294, USA
J Bacteriol 182:4343-7. 2000..Tn4001T may be of general utility for use as a mycoplasma cloning vehicle because tetM functions in all species of Mycoplasma examined thus far...
Identification of exopolysaccharide-deficient mutants of Mycoplasma pulmonisJames M Daubenspeck
Department of Microbiology, University of Alabama at Birmingham, Birmingham, AL 35294, USA
Mol Microbiol 72:1235-45. 2009..Confounding the interpretation of these results is the observation that the mutants missing EPS-I had an eightfold overproduction of an apparent second EPS (EPS-II) containing N-acetylglucosamine...
A stochastic mechanism for biofilm formation by Mycoplasma pulmonisWarren L Simmons
Department of Genetics, University of Alabama at Birmingham, Birmingham AL 35294 0004, USA
J Bacteriol 189:1905-13. 2007..As variation in the number of Vsa tandem repeats occurs by slipped-strand mispairing, the ability of the mycoplasmas to form a biofilm switches stochastically...
Mycoplasma biofilms ex vivo and in vivoWarren L Simmons
Department of Genetics, University of Alabama at Birmingham, Birmingham, AL 35294 0024, USA
FEMS Microbiol Lett 295:77-81. 2009..This tracheal organ-mounting system can be used to study interactions between biofilms formed by respiratory pathogens and the host epithelium and to identify the factors that contribute to biofilm formation in vivo...
Biofilms protect Mycoplasma pulmonis cells from lytic effects of complement and gramicidinWarren L Simmons
Department of Genetics, University of Alabama at Birmingham, KAUL 720, Birmingham, AL 35294 0004, USA
Infect Immun 75:3696-9. 2007..The resistance appeared to be localized to those mycoplasmas within tower structures of the biofilms. Biofilm formation may be a mechanism that protects mycoplasmas from host immunity...
The Vsa proteins modulate susceptibility of Mycoplasma pulmonis to complement killing, hemadsorption, and adherence to polystyreneWarren L Simmons
Department of Genetics, University of Alabama at Birmingham, 720 South 20th Street, Kaul Room 720, Birmingham, AL 35294, USA
Infect Immun 71:5733-8. 2003..As both VsaH and VsaA can mediate adherence to plastic, cytadherence, and susceptibility to complement, we propose that Vsa modulates these phenotypes by nonspecific interactions...
Resistance of Mycoplasma pulmonis to complement lysis is dependent on the number of Vsa tandem repeats: shield hypothesisWarren L Simmons
Department of Genetics, University of Alabama at Birmingham, 720 South 20th Street, Kaul Room 720, Birmingham, AL 35294 0024, USA
Infect Immun 72:6846-51. 2004..pulmonis surface interactions and function to sterically hinder access of complement to the mycoplasma cell membrane while permitting access of smaller molecules...
Large-scale transposon mutagenesis of Mycoplasma pulmonisChristopher T French
Department of Genetics, University of Alabama Birmingham, Birmingham, AL 35294, USA
Mol Microbiol 69:67-76. 2008..A mutant with a defect in transport of N-acetylglucosamine was identified...
Avoidance of the host immune system through phase variation in Mycoplasma pulmonisAmy M Denison
Department of Genetics, KAUL, Room 720, University of Alabama at Birmingham, Birmingham, AL 35294-0024, USA
Infect Immun 73:2033-9. 2005..The data strongly indicate that Vsa phase variation is a mechanism for avoidance of the immune system with no obvious contribution to tissue tropism...
The vir gene of bacteriophage MAV1 confers resistance to phage infection on Mycoplasma arthritidisBrenda Clapper
Department of Microbiology, KAUL, Rm 720, University of Alabama at Birmingham, Birmingham, AL 35294 0024, USA
J Bacteriol 186:5715-20. 2004..Vir had no effect on MAV1 adsorption. We conclude that Vir is not a virulence factor but functions to exclude superinfecting phage, possibly by blocking the injection of phage DNA into the bacterial cytoplasm...
Association of Mycoplasma arthritidis mitogen with lethal toxicity but not with arthritis in miceWenyi Luo
Department of Genetics, University of Alabama at Birmingham, Birmingham, AL 35294 0024, USA
Infect Immun 76:4989-98. 2008..The degree of mitogenic activity correlated with lethal toxicity in DBA/2J mice. In contrast, histopathological studies detected no correlation between MAM production and the severity of arthritis induced in DBA/2J and CBA/J mice...
Gene transfer in Mycoplasma pulmonisAmy M Teachman
Department of Pathology, University of Alabama at Birmingham, Birmingham, Alabama 35294, USA
J Bacteriol 184:947-51. 2002..Analysis of the progeny indicated that only the transposon and not flanking genomic DNA was transferred to the recipient cell. Gene transfer was DNase resistant and probably the result of conjugation or cell fusion...
Bacteriophage MAV1 is not associated with virulence of Mycoplasma arthritidisBrenda Clapper
Department of Genetics, KAUL, Room 720, University of Alabama at Birmingham, Birmingham, AL 35294 0024, USA
Infect Immun 72:7322-5. 2004..The virulence of 158 and 158-1 did not increase upon lysogenization. A major antigenic difference between 158 and 158-1 was identified that is unrelated to MAV1 and could account for the difference in virulence...
Trinucleotide GAA repeats dictate pMGA gene expression in Mycoplasma gallisepticum by affecting spacing between flanking regionsLi Liu
Department of Genomics and Pathobiology, Volker Hall, University of Alabama at Birmingham, Birmingham, AL 35294, USA
J Bacteriol 184:1335-9. 2002..These data indicate that the nucleotides 5" of the GAA repeats as well as the spacing between the GAA repeats and sequences downstream (3") of the repeats are important for pMGA gene expression...
Role of bacteriophage MAV1 as a mycoplasmal virulence factor for the development of arthritis in mice and ratsAnh-Hue T Tu
Department of Genomics and Pathobiology, University of Alabama at Birmingham, 35294-0019, USA
J Infect Dis 186:432-5. 2002..Specifically, the MAV1 lysogen 158L3-1 was more virulent than the nonlysogen strain 158 in DBA/2NCr, C3H/HeNCr, C3H/HeJ, and C3Smn.CB17-Prkdc(scid)/J mice, as well as in LEW rats...
A unique, bifunctional site-specific DNA recombinase from Mycoplasma pulmonisRamakrishnan Sitaraman
Departments of Genomics and Pathobiology, University of Alabama at Birmingham, AL 35294, USA
Mol Microbiol 46:1033-40. 2002..Thus, HvsR is a site-specific DNA recombinase with dual substrate specificity...
Identification of an isoschizomer of the HhaI DNA methyltransferase in Mycoplasma arthritidisWenyi Luo
Department of Genetics, University of Alabama at Birmingham, Birmingham, AL 35294 0024, USA
FEMS Microbiol Lett 290:195-8. 2009..Transformation of M. arthritidis was not significantly affected by modification of plasmid at HhaI sites, indicating that the mycoplasma lacks a restriction endonuclease that recognizes GCGC sites...
Research Grants
- Tandemly Repetitive Proteins in MycoplasmasKevin Dybvig; Fiscal Year: 2007..By understanding the role of repetitive proteins in the disease process, it is anticipated that improved measures to control the infections of these significant human pathogens will be developed. ..
- Mechanisms of Mycoplasmal Disease PathogenesisKevin Dybvig; Fiscal Year: 2009..Mutants that do not survive will be characterized further to determine whether their defect is a failure to grow in vivo, to adhere to the epithelium, or to resist host defenses. ..
- MECHANISMS OF MYCOPLASMA-INDUCED ARTHRITISKevin Dybvig; Fiscal Year: 2009..An understanding of the inability of 158-1 to resist host defenses may offer an unique opportunity to explore interactions between the mycoplasma and innate immunity. ..
- ANTIGENIC VARIATION IN MYCOPLASMASKevin Dybvig; Fiscal Year: 2004....
- MECHANISMS OF MYCOPLASMA INDUCED ARTHRITISKevin Dybvig; Fiscal Year: 1999..arthritidis chromosome and/or specifically mutated to construct strains that will be examined for arthritogenicity in the rat model and used to conclusively identify the MAV1 genes that are involved in the development of arthritis. ..
- GENETIC RECOMBINATION IN MYCOPLASMASKevin Dybvig; Fiscal Year: 2000..The fifth and final aim is to expand our repertoire of subclones containing DNA inversions and other rearrangements in order to more fully characterize the potential for genetic variation in this system. ..
- MECHANISMS OF MYCOPLASMA-INDUCED ARTHRITISKevin Dybvig; Fiscal Year: 2002..arthritidis by affecting interactions with host factors such as B and T cells and complement. Thus, the process of dissecting the function of MAV1 in virulence will be begun. ..
- GENETIC RECOMBINATION IN MYCOPLASMASKevin Dybvig; Fiscal Year: 2004..In aim 2, mutants with defects in putative DNA recombinases and V-I protein production will be examined to study the mechanisms of gene rearrangements and phenotypic switching. ..
- Tandemly Repetitive Proteins in MycoplasmasKEVIN F DYBVIG; Fiscal Year: 2010..By understanding the role of repetitive proteins in the disease process, it is anticipated that improved measures to control the infections of these significant human pathogens will be developed. ..
