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Which genes does P. gingivalis need to grow?

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A near-saturating Tn-seq screen finds ~463 (~22%) P. gingivalis genes putatively essential on blood agar.

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Identification of essential genes of the periodontal pathogen Porphyromonas gingivalis

Klein BA, Tenorio EL, Lazinski DW, et al. · BMC genomics · 2012

doi.org/10.1186/1471-2164-13-578Read the full paper ↗123 citationscc by

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Which genes does P. gingivalis need to grow?

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463 (22.0%) genes putatively essential for in vitro survival.

Applying these rules, out of a total 2,102 genes in the ATCC 33277 genome (all protein coding sequences and rRNA genes combined minus the 53 tRNAs), we identified 463 (22.0%) genes as putatively essential for in vitro survival (described below) (Figure ) (Additional file : Table S1).

78.6% of putative essentials have known essential homologues.

gingivalis , 364 (78.6%) have known essential gene homologues determined by BLASTP interrogation of the DEG ( http://tubic.tju.edu.cn/deg/ ), version 6.8, updated on November 4, 2011 (Additional file : Table S1) [,].
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What they did

Authors built a Mariner Tn-seq library in P. gingivalis ATCC 33277 and scored insertion under-representation to call genes required for in vitro survival on blood agar.

What they found

463 genes (22%) are putatively essential; most have essential homologues elsewhere, while ~21% may be species/niche-specific essentials.

The limits

What it doesn't show

Blood-agar essentials ≠ all virulence genes in the host; different selective pressures will reveal other gene sets.

Key terms

Tn-seq
Transposon insertion sequencing to find essential/conditioned genes.
Essential gene
Gene required for growth under the tested condition.
Porphyromonas gingivalis
Oral anaerobic keystone pathogen linked to periodontitis.
Mariner transposon
Mobile element inserting primarily at TA dinucleotides.
Keystone pathogen
Microbe whose presence disproportionately reshapes community and disease.

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Putative essential gene count:

Common questions

How many essentials were called?

463 genes (~22%).

What growth condition?

In vitro survival/growth on blood agar.

What method?

Mariner Tn-seq with quantitative sequencing.

Are all essentials universal?

No—about 21% lack DEG homologues and may be niche-specific.

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