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Published on: July 15, 2011
The Cipher Code of Simple Sequence Repeats in "Vampire Pathogens"
Geng Zou1, Bernardo Bello-Orti2, Virginia Aragon3
1State Key Laboratory of Agricultural Microbiology, College of Veterinary Medicine, Huazhong Agricultural University, Wuhan 430070, China.
Abstract:
Blood inside mammals is a forbidden area for the majority of prokaryotic microbes; however, red blood cells tropism microbes, like "vampire pathogens" (VP), succeed in matching scarce nutrients and surviving strong immunity reactions. Here, we found VP of Mycoplasma, Rhizobiales, and Rickettsiales showed significantly higher counts of (AG)n dimeric simple sequence repeats (Di-SSRs) in the genomes, coding and non-coding regions than non Vampire Pathogens (N_VP). Regression analysis indicated a significant correlation between GC content and the span of (AG)n-Di-SSR variation. Gene Ontology (GO) terms with abundance of (AG)3-Di-SSRs shared by the VP strains were associated with purine nucleotide metabolism (FDR < 0.01), indicating an adaptation to the limited availability of purine and nucleotide precursors in blood. Di-amino acids coded by (AG)n-Di-SSRs included all three six-fold code amino acids (Arg, Leu and Ser) and significantly higher counts of Di-amino acids coded by (AG)3, (GA)3, and (TC)3 in VP than N_VP. Furthermore, significant differences (P < 0.001) on the numbers of triplexes formed from (AG)n-Di-SSRs between VP and N_VP in Mycoplasma suggested the potential role of (AG)n-Di-SSRs in gene regulation.
Insights
Vampire pathogens (VP) inhabiting mammalian blood exhibit higher (AG)n dimeric simple sequence repeats (Di-SSRs) in their genomes. These repeats correlate with purine metabolism adaptations and amino acid variations, suggesting survival strategies in nutrient-scarce environments.
Area of Science:
- Microbiology
- Genomics
- Bioinformatics
Background:
- Mammalian blood presents a challenging environment for most prokaryotic microbes.
- Certain microbes, termed "vampire pathogens" (VP), have adapted to survive within red blood cells, accessing scarce nutrients and evading host immunity.
Purpose of the Study:
- To investigate genomic differences, specifically simple sequence repeats (SSRs), between VP and non-VP (N_VP) microbes.
- To explore the functional implications of observed genomic variations in VP adaptation to the blood environment.
Main Methods:
- Comparative genomic analysis of VP and N_VP strains.
- Identification and quantification of dimeric simple sequence repeats (Di-SSRs), particularly (AG)n repeats.
- Regression analysis to correlate SSRs with genomic features like GC content.
- Gene Ontology (GO) term enrichment analysis to identify functional associations.
- Analysis of amino acid variations resulting from SSRs.
Main Results:
- VP strains showed significantly higher counts of (AG)n Di-SSRs in both coding and non-coding genomic regions compared to N_VP.
- A significant correlation was found between GC content and the variation span of (AG)n-Di-SSRs.
- VP strains with abundant (AG)3-Di-SSRs were associated with purine nucleotide metabolism pathways, indicating adaptation to low-purine environments.
- Di-amino acids encoded by (AG)n-Di-SSRs included Arg, Leu, and Ser, with higher counts in VP.
- Mycoplasma VP exhibited significant differences in triplex formation from (AG)n-Di-SSRs compared to N_VP, suggesting a role in gene regulation.
Conclusions:
- Elevated (AG)n Di-SSRs are a genomic characteristic of vampire pathogens, potentially aiding their adaptation to the mammalian blood environment.
- (AG)n-Di-SSRs are linked to purine metabolism and amino acid composition, reflecting nutrient acquisition strategies.
- The findings suggest that (AG)n-Di-SSRs play a role in the gene regulation and survival of blood-dwelling prokaryotes.
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