Strain and Virulence Diversity in the Mouse Pathogen Chlamydia muridarum

• Published in: Infection and Immunity Vol. 77; no. 8; pp. 3284 - 3293
• Main Authors: Ramsey, Kyle H, Sigar, Ira M, Schripsema, Justin H, Denman, Cecele J, Bowlin, Anne K, Myers, Garry A.S, Rank, Roger G
• Format: Journal Article
• Language: English
• Published: Washington, DC American Society for Microbiology 01.08.2009; American Society for Microbiology (ASM)
• Subjects: Adenocarcinoma; Animal models; Animals; Bacterial Infections; Bacteriology; Biological and medical sciences; Chlamydia muridarum - genetics; Chlamydia muridarum - pathogenicity; Chlamydia trachomatis; Data processing; DNA, Bacterial - chemistry; DNA, Bacterial - genetics; Epithelial Cells - microbiology; Female; Fibroblasts; Fundamental and applied biological sciences. Psychology; Gene deletion; Genetic Variation; genomics; HeLa Cells; Humans; Immunity; Inclusion Bodies - microbiology; Infection; Insertion; Lethal Dose 50; Lung - microbiology; Mice; Microbiology; Miscellaneous; Molecular Sequence Data; Mutagenesis, Insertional; Mutation; Pathogens; Plaques; Polymorphism, Single Nucleotide; Respiratory tract diseases; Sequence Analysis, DNA; Sequence Deletion; Single-nucleotide polymorphism; Survival Analysis; Vagina - microbiology; Virulence; Vertebrata; Mammalia; Chlamydiaceae; Chlamydia; Microbiology; Mouse; Virulence; Rodentia; Chlamydiales; Bacteria; Immunity; Strain
• DOI: 10.1128/IAI.00147-09
• ISSN: 0019-9567

The mouse chlamydial pathogen Chlamydia muridarum has been used as a model organism for the study of human Chlamydia trachomatis urogenital and respiratory tract infections. To date, two commonly used C. muridarum isolates have been used interchangeably and are essentially taken to be identical. Herein, we present data that indicate that this is not the case. The C. muridarum Weiss isolate and C. muridarum Nigg isolate varied significantly in their virulences in vivo and possessed different growth characteristics in vitro. Distinct differences were observed in intravaginal 50% infectious doses and in challenge infections, with the Weiss isolate displaying greater virulence. Respiratory infection by the intranasal route also indicated a greater virulence of the Weiss isolate. In vitro, morphometric analysis revealed that the Weiss isolate produced consistently smaller inclusions in human cervical adenocarcinoma cells (HeLa 229) and smaller plaques in monolayers of mouse fibroblasts (L929) than did the Nigg isolate. In addition, the Weiss isolate possessed significantly higher replicative yields in vitro than did the Nigg isolate. In plaque-purified isolates derived from our stocks of these two strains, total genomic sequencing identified several unique nonsynonymous single nucleotide polymorphisms and insertion/deletion mutations when our Weiss (n = 4) and Nigg (n = 5) isolates were compared with the published Nigg sequence. In addition, the two isolates shared 11 mutations compared to the published Nigg sequence. These results prove that there is genotypic and virulence diversity among C. muridarum isolates. These findings can be exploited to determine factors related to chlamydial virulence and immunity.