| Literature DB >> 27460796 |
Elodie Ramond1, Catherine Maclachlan2, Stéphanie Clerc-Rosset2, Graham W Knott2, Bruno Lemaitre1.
Abstract
UNLABELLED: Spiroplasma bacteria are highly motile bacteria with no cell wall and a helical morphology. This clade includes many vertically transmitted insect endosymbionts, including Spiroplasma poulsonii, a natural endosymbiont of Drosophila melanogaster S. poulsonii bacteria are mainly found in the hemolymph of infected female flies and exhibit efficient vertical transmission from mother to offspring. As is the case for many facultative endosymbionts, S. poulsonii can manipulate the reproduction of its host; in particular, S. poulsonii induces male killing in Drosophila melanogaster Here, we analyze the morphology of S. poulsonii obtained from the hemolymph of infected Drosophila This endosymbiont was not only found as long helical filaments, as previously described, but was also found in a Y-shaped form. The use of electron microscopy, immunogold staining of the FtsZ protein, and antibiotic treatment unambiguously linked the Y shape of S. poulsonii to cell division. Observation of the Y shape in another Spiroplasma, S. citri, and anecdotic observations from the literature suggest that cell division by longitudinal scission might be prevalent in the Spiroplasma clade. Our study is the first to report the Y-shape mode of cell division in an endosymbiotic bacterium and adds Spiroplasma to the so far limited group of bacteria known to utilize this cell division mode. IMPORTANCE: Most bacteria rely on binary fission, which involves elongation of the bacteria and DNA replication, followed by splitting into two parts. Examples of bacteria with a Y-shape longitudinal scission remain scarce. Here, we report that Spiroplasma poulsonii, an endosymbiotic bacterium living inside the fruit fly Drosophila melanogaster, divide with the longitudinal mode of cell division. Observations of the Y shape in another Spiroplasma, S. citri, suggest that this mode of scission might be prevalent in the Spiroplasma clade. Spiroplasma bacteria are wall-less bacteria with a distinctive helical shape, and these bacteria are always associated with arthropods, notably insects. Our study raises the hypothesis that this mode of cell division by longitudinal scission could be linked to the symbiotic mode of life of these bacteria.Entities:
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Year: 2016 PMID: 27460796 PMCID: PMC4981714 DOI: 10.1128/mBio.00881-16
Source DB: PubMed Journal: MBio Impact factor: 7.867
FIG 1 Presence of Y-shaped S. poulsonii in Drosophila hemolymph samples. (A and B) Fluorescence microscopy images showing SYTO9-stained S. poulsonii from freshly extracted hemolymph from 1-week-old Drosophila melanogaster flies. Bars, 1 µm. (C to F) SEM of S. poulsonii extracted from 1-week-old Spiroplasma-infected female flies. S. poulsonii can be found as one elongated body (C) or with a Y-shape conformation (D to F) with variation in the length of the arms. Bars, 1 µm. (G and zoom in G′) TEM of S. poulsonii from freshly extracted Drosophila hemolymph. The white arrowhead shows the branching. Bar, 1 µm. (H) Immunogold labeling pattern of the FtsZ protein with an anti-FtsZ antibody. Y-shaped bacteria have two FtsZ protein aggregates. Bar, 200 nm. (I and J) SEM of in vitro-cultured S. citri. S. citri can be found as one elongated body (I) or with a Y-shaped conformation (J). Bars, 1 µm. The presence of aggregates might be due to protein enrichment in the medium used to cultivate S. citri.
FIG 2 Impacts of various antibiotics on the Y-shaped form of Spiroplasma. (A to E) SEM of S. poulsonii extracted from Spiroplasma-infected female flies injected with phosphate-buffered saline (PBS) (A), DMSO (B), ethanol (C), PC190723 (D), or ciprofloxacin (E). One-week-old females were injected with molecules, and hemolymph was extracted after 4 days. Bars, 500 nm. (F) Quantification of normal and abnormal Y-shape S. poulsonii by SEM in hemolymph samples collected from treated flies. ***, P < 0.005. Values are means plus standard deviations (SD) (error bars) of data pooled from three independent experiments with 100 bacteria for each count. Twenty flies were used to extract fresh hemolymph for each experiment. (G) Evaluation of bacterial count per fly following each treatment. Spiroplasma bacteria were counted 1 week after injection. **, P < 0.01; ***, P < 0.005. Values are means plus SD of data pooled from three independent experiments with 20 flies for each count. (H) Quantification of the amount of fluorescence per bacteria. DNA fluorescence per Spiroplasma was measured 4 days after injection. *, P < 0.05; **, P < 0.01. Values are means plus SD of data pooled from three independent experiments with 20 flies tested for each count.