TY - JOUR
T1 - Different growth rates of Chlamydia trachomatis biovars reflect pathotype
AU - Miyairi, Isao
AU - Mahdi, Olaimatu S.
AU - Ouellette, Scot P.
AU - Belland, Robert J.
AU - Byrne, Gerald I.
N1 - Funding Information:
Received 4 January 2006; accepted 24 February 2006; electronically published 22 June 2006. Presented in part: 5th Meeting of the European Society for Chlamydia Research, 1–4 September 2004, Budapest, Hungary. Potential conflicts of interest: none reported. Financial support: Public Health Service Grants (Immunity and Latency Grant AI 19782 to G.I.B.); Children’s Foundation Research Center and LeBonheur Children’s Medical Center Small Grant (to I.M.); St. Jude Children’s Research Hospital (fellowship grant to I.M.). Reprints or correspondence: Dr. Gerald I. Byrne, Dept. of Molecular Sciences, University of Tennessee Health Science Center, 858 Madison Ave., Memphis, TN 38163 (gbyrne@utmem.edu).
PY - 2006/8/1
Y1 - 2006/8/1
N2 - Background. Despite small genomic differences, Chlamydia trachomatis biovars exhibit diverse disease manifestations and different growth rates in vivo and in cell culture models. Methods. Chlamydial inclusion-forming units were enumerated over time in HeLa cells, to evaluate the length of the developmental cycle for C. trachomatis strains A, B, C, and E/Bour (ocular strains) as well as D, E/UW5/ Cx, F, and L2 (genital strains). Prototype strains A, D, and L2 were selected for detailed analysis of reticulate body growth, division, and genomic replication. The impact that changing host cells and that coinfection with different strains has on growth was also assessed. Results. The genital strains completed the developmental cycle in 36-44 h, whereas the ocular strains lagged behind considerably. Differences were the result of a longer lag phase (entry plus differentiation) and generation time for the ocular strains. A prototype ocular strain grew faster in conjunctival cells than in cervical cells. Coinfection with genital (D or L2) and ocular strains expedited recovery of the ocular strain. Conclusions. Precise temporal evaluation of the chlamydial developmental cycle for selected genital and ocular C. trachomatis biovars provides a means for investigating genomic differences that define chlamydial pathotype.
AB - Background. Despite small genomic differences, Chlamydia trachomatis biovars exhibit diverse disease manifestations and different growth rates in vivo and in cell culture models. Methods. Chlamydial inclusion-forming units were enumerated over time in HeLa cells, to evaluate the length of the developmental cycle for C. trachomatis strains A, B, C, and E/Bour (ocular strains) as well as D, E/UW5/ Cx, F, and L2 (genital strains). Prototype strains A, D, and L2 were selected for detailed analysis of reticulate body growth, division, and genomic replication. The impact that changing host cells and that coinfection with different strains has on growth was also assessed. Results. The genital strains completed the developmental cycle in 36-44 h, whereas the ocular strains lagged behind considerably. Differences were the result of a longer lag phase (entry plus differentiation) and generation time for the ocular strains. A prototype ocular strain grew faster in conjunctival cells than in cervical cells. Coinfection with genital (D or L2) and ocular strains expedited recovery of the ocular strain. Conclusions. Precise temporal evaluation of the chlamydial developmental cycle for selected genital and ocular C. trachomatis biovars provides a means for investigating genomic differences that define chlamydial pathotype.
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U2 - 10.1086/505432
DO - 10.1086/505432
M3 - Article
C2 - 16826483
AN - SCOPUS:33746368736
SN - 0022-1899
VL - 194
SP - 350
EP - 357
JO - Journal of Infectious Diseases
JF - Journal of Infectious Diseases
IS - 3
ER -