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Published on: June 10, 2020
In vitro analysis of genetically distinct Chlamydia pecorum isolates reveals key growth differences in mammalian
Md Mominul Islam1, Martina Jelocnik1, Susan Anstey1
1Genecology Research Centre, Faculty of Science, Health, Education and Engineering, University of the Sunshine Coast, Sippy Downs, Australia.
Abstract:
Chlamydia (C.) pecorum is an obligate intracellular bacterium that infects and causes disease in a broad range of animal hosts. Molecular studies have revealed that this pathogen is genetically diverse with certain isolates linked to different disease outcomes. Limited in vitro or in vivo data exist to support these observations, further hampering efforts to improve our understanding of C. pecorum pathogenesis. In this study, we evaluated whether genetically distinct C. pecorum isolates (IPA, E58, 1710S, W73, JP-1-751) display different in vitro growth phenotypes in different mammalian epithelial and immune cells. In McCoy cells, shorter lag phases were observed for W73 and JP-1-751 isolates. Significantly smaller inclusions were observed for the naturally plasmid-free E58 isolate. C. pecorum isolates of bovine (E58) and ovine origin (IPA, W73, JP-1-751) grew faster in bovine cells compared to a porcine isolate (1710S). C. pecorum isolates could infect but appear not able to complete their developmental cycle in bovine peripheral neutrophil granulocytes. All isolates, except 1710S, could multiply in bovine monocyte-derived macrophages. These results reveal potentially important phenotypic differences that will help to understand the pathogenesis of C. pecorum in vivo and to identify C. pecorum virulence factors.
Insights
Distinct Chlamydia (C.) pecorum strains show varied growth in different animal cells, impacting our understanding of C. pecorum pathogenesis and virulence factors.
Area of Science:
- Veterinary Microbiology
- Bacterial Pathogenesis
- Cell Biology
Background:
- Chlamydia (C.) pecorum is a genetically diverse bacterium causing varied diseases in animals.
- Limited data exist on C. pecorum pathogenesis and the impact of genetic diversity on disease outcomes.
- Understanding C. pecorum virulence factors requires more in vitro and in vivo data.
Purpose of the Study:
- To investigate if distinct C. pecorum isolates exhibit different in vitro growth phenotypes.
- To compare the growth of various C. pecorum isolates in different mammalian epithelial and immune cells.
- To identify potential C. pecorum virulence factors linked to observed phenotypic differences.
Main Methods:
- In vitro culture of five distinct C. pecorum isolates (IPA, E58, 1710S, W73, JP-1-751).
- Growth assessment in McCoy cells, bovine peripheral neutrophil granulocytes, and bovine monocyte-derived macrophages.
- Analysis of inclusion size and lag phase as indicators of growth phenotype.
Main Results:
- Isolates W73 and JP-1-751 showed shorter lag phases in McCoy cells.
- The plasmid-free E58 isolate formed significantly smaller inclusions.
- Bovine and ovine isolates grew faster in bovine cells than the porcine isolate (1710S).
- Neutrophils supported infection but not complete development; macrophages supported multiplication for most isolates.
Conclusions:
- Genetically distinct C. pecorum isolates display significant phenotypic differences in vitro.
- These differences in growth and replication provide insights into C. pecorum pathogenesis.
- The findings aid in identifying C. pecorum virulence factors and understanding host-pathogen interactions.
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