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Genomic variations leading to alterations in cell morphology of Campylobacter spp
Campylobacter jejuni, the most common cause of bacterial diarrhoeal disease, is normally helical. However, it can also adopt straight rod, elongated helical and coccoid forms. Studying how helical morphology is generated, and how it switches between its different forms, is an important objective for...
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Published in: | Scientific reports 2016-12, Vol.6 (1), p.38303, Article 38303 |
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Main Authors: | , , , , , , , , , , , , , , , , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that this one cites Items that cite this one |
Online Access: | Get full text |
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Summary: | Campylobacter jejuni,
the most common cause of bacterial diarrhoeal disease, is normally helical. However, it can also adopt straight rod, elongated helical and coccoid forms. Studying how helical morphology is generated, and how it switches between its different forms, is an important objective for understanding this pathogen. Here, we aimed to determine the genetic factors involved in generating the helical shape of
Campylobacter
. A
C. jejuni
transposon (Tn) mutant library was screened for non-helical mutants with inconsistent results. Whole genome sequence variation and morphological trends within this Tn library, and in various
C. jejuni
wild type strains, were compared and correlated to detect genomic elements associated with helical and rod morphologies. All rod-shaped
C. jejuni
Tn mutants and all rod-shaped laboratory, clinical and environmental
C. jejuni
and
Campylobacter coli
contained genetic changes within the
pgp1
or
pgp2
genes, which encode peptidoglycan modifying enzymes. We therefore confirm the importance of Pgp1 and Pgp2 in the maintenance of helical shape and extended this to a wide range of
C. jejuni
and
C. coli
isolates. Genome sequence analysis revealed variation in the sequence and length of homopolymeric tracts found within these genes, providing a potential mechanism of phase variation of cell shape. |
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ISSN: | 2045-2322 2045-2322 |
DOI: | 10.1038/srep38303 |