Abstract

Bacterial behavior and virulence during human infection is difficult to study and largely unknown, as our vast knowledge of infection microbiology is primarily derived from studies using invitro and animal models. Here, we characterize the physiology of Porphyromonas gingivalis, a periodontal pathogen, in its native environment using 93 published metatranscriptomic datasets from periodontally healthy and diseased individuals. P. gingivalis transcripts were more abundant in samples from periodontally diseased patients but only above 0.1% relative abundance in one-third of diseased samples. During human infection, P. gingivalis highly expressed genes encoding virulence factors such as fimbriae and gingipains (proteases) and genes involved in growth and metabolism, indicating that P. gingivalis is actively growing during disease. A quantitative framework for assessing the accuracy of model systems showed that 96% of P. gingivalis genes were expressed similarly in periodontitis and invitro midlogarithmic growth, while significantly fewer genes were expressed similarly in periodontitis and invitro stationary phase cultures (72%) or in a murine abscess infection model (85%). This high conservation in gene expression between periodontitis and logarithmic laboratory growth is driven by overall low variance in P. gingivalis gene expression, relative to other pathogens including Pseudomonas aeruginosa and Staphylococcus aureus Together, this study presents strong evidence for the use of simple test tube growth as the gold standard model for studying P. gingivalis biology, providing biological relevance for the thousands of laboratory experiments performed with logarithmic phase P. gingivalis Furthermore, this work highlights the need to quantitatively assess the accuracy of model systems.

Highlights

  • The ultimate goal of the vast majority of microbiology research is to understand the processes that shape microbial behavior, ecology, and evolution, ranging from studies of the microbial role in pathogenesis to the microbial contribution to nutrient cycling in the oceans

  • We discovered that P. gingivalis highly expressed a number of virulence factors, including the Arg- and Lys-gingipains, and genes related to growth and metabolism during periodontal disease

  • We mapped the mock metatranscriptomes to the P. gingivalis American Type Culture Collection (ATCC) 33277 genome and to a pangenome of P. gingivalis strains

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Summary

Introduction

The ultimate goal of the vast majority of microbiology research is to understand the processes that shape microbial behavior, ecology, and evolution, ranging from studies of the microbial role in pathogenesis to the microbial contribution to nutrient cycling in the oceans. P. gingivalis is an obligate anaerobe and is asaccharolytic, using amino acids as its primary carbon source This microbe is often associated with chronic periodontitis, and it has been characterized as a keystone pathogen because of its ability to alter the oral immune environment, leading to dysbiosis of the microbial community as a whole (9). Most microbial knowledge comes from experiments in laboratory models, despite the assumption that these artificial systems alter microbial physiology relative the native environment We tested this assumption for an oral pathogen, Porphyromonas gingivalis, using 93 metatranscriptomes from periodontally healthy and diseased patients and 122 transcriptomes from experimental models. We discovered that a simple in vitro model, midlogarithmic growth in rich media, highly recapitulates P. gingivalis gene expression in the human oral cavity, outperforming other models, including a murine infection model These results support the biological relevance of decades of laboratory experiments with this pathogen and validate an accessible experimental model for studying P. gingivalis biology. These data provide a conceptual framework for understanding in situ gene expression across microbes

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