Schineria larvae gen. nov., sp. nov., isolated from the 1st and 2nd larval stages of Wohlfahrtia magnifica (Diptera: Sarcophagidae).

Tóth, Erika; Kovács, Gábor M.; Schümann, Peter; Kovács, Attila; Steiner, Ulrike; Halbritter, András; Màrialigeti, Károly

doi:10.1099/00207713-51-2-401

Cited by 70 publications

(53 citation statements)

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“…Two Gram-negative-staining, aerobic, non-motile, rod-shaped bacteria, designated strains FFA1 The genus Ignatzschineria (formerly known by the illegitimate name Schineria) was first described by Tó th et al (2001Tó th et al ( , 2007. This genus belongs to the class Gammaproteobacteria and, at present, comprises only one recognized species, Ignatzschineria larvae.…”

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“…This genus belongs to the class Gammaproteobacteria and, at present, comprises only one recognized species, Ignatzschineria larvae. This species was isolated from the first and second larval stages of an obligate parasitic fly, Wohlfahrtia magnifica (Diptera: Sarcophagidae), responsible for myiasis (Tó th et al, 2001(Tó th et al, , 2006. The genus is characterized by aerobic, Gramnegative, non-spore-forming, non-motile and regular rod-shaped bacteria.…”

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“…For comparative analyses, strains I. larvae L1/68 T and W. chitiniclastica S5 T were obtained from Dr Erika M. Tó th (Tó th et al, 2001(Tó th et al, , 2008. All of the phenotypic tests described below were performed on strains FFA1…”

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“…Utilization of citrate was checked according to the method of Simmons (1926). Chitinase activity was studied as described by Holding & Collee (1971) and modified by Tó th et al (2001) and O'Brien & Colwell (1987). The classic medium of Koser (1923), as modified by Ventosa et al (1982) L-tyrosine and L-valine. Results were interpreted according to Ventosa et al (1982) after incubation at 37 u C for 3 days under aerobic conditions.…”

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Ignatzschineria indica sp. nov. and Ignatzschineria ureiclastica sp. nov., isolated from adult flesh flies (Diptera: Sarcophagidae)

Gupta

Dharne

Rangrez

et al. 2011

International Journal of Systematic and Evolutionary Microbiology

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Two Gram-negative-staining, aerobic, non-motile, rod-shaped bacteria, designated strains FFA1T and FFA3T, and belonging to the class Gammaproteobacteria were isolated from the gastrointestinal tract of adult flesh flies (Diptera: Sarcophagidae). Phylogenetic analysis of 16S rRNA gene sequence data placed these two strains within the genus Ignatzschineria with similarities of 98.6 % (FFA1T) and 99.35 % (FFA3T) to Ignatzschineria larvae L1/68T. The level of gene sequence similarity between strains FFA1T and FFA3T was 99 %, 97.15 % and 78.1 % based on the 16S rRNA, 23S rRNA and gyrB gene sequences, respectively. Strains FFA1T and FFA3T shared 24 % DNA–DNA relatedness. DNA–DNA hybridization revealed a very low level of relatedness between the novel strains (22 % for strain FFA1T and 44 % for strain FFA3T) and I. larvae L1/68T genomic DNA. The respiratory quinone was Q-8 in both novel strains. The DNA G+C contents were 41.1 mol% and 40.1 mol% for strains FFA1T and FFA3T, respectively. The cell membrane of both strains consisted of phosphatidylglycerol, phosphatidylethanolamine, phospholipids and aminophospholipid. The major fatty acids for both strains were C16 : 0, summed feature 8 (C18 : 1ω7c and/or C18 : 1ω6c), CyC19 : 0ω8c and C14 : 0. The results of DNA–DNA hybridization between the two new strains and I. larvae L1/68T, in combination with phylogenetic, chemotaxonomic, biochemical and electron microscopic data, demonstrated that strains FFA1T and FFA3T represented two novel species of the genus Ignatzschineria for which the names Ignatzschineria indica sp. nov. (type strain FFA1T = DSM 22309T = KCTC 22643T = NCIM 5325T) and Ignatzschineria ureiclastica sp. nov. (type strain FFA3T = DSM 22310T = KCTC 22644T = NCIM 5326T) are proposed.

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Ignatzschineria indica sp. nov. and Ignatzschineria ureiclastica sp. nov., isolated from adult flesh flies (Diptera: Sarcophagidae)

Gupta

Dharne

Rangrez

et al. 2011

International Journal of Systematic and Evolutionary Microbiology

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“…It is amazing to see how different the various prokaryotes can be. [61][62][63] To observe for example genetically manipulated HIV viruses budding off tissue culture cells is also a special experience. 64 My knowledge about science developed through my activity in autophagy research.…”

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Kovács

Klionsky

2013

Autophagy

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Schineria

2015

Bergey's Manual of Systematics of Archaea and Bacteria

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Schi' ner.i.a . N.L. fem. n. Schineria pertaining to Schiner who first described the fly Wohlfahrtia magnifica in 1862. Proteobacteria / Gammaproteobacteria / Xanthomonadales / Xanthomonadaceae / Schineria Gram‐negative nonmotile aerobic rods . Catalase positive. Major fatty acids, C 14:0 , C 16:0 , and C 18:1 . Major polar lipids include phosphatidylethanolamine, phosphatidylglycerol, and phosphatidylserine. The mol % G + C of the DNA is : 42 (HPLC). Type species : Schineria larvae Tóth, Kovács, Schumann, Kovács, Steiner, Halbritter and Máriageti 2001, 406.

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Schineria larvae gen. nov., sp. nov., isolated from the 1st and 2nd larval stages of Wohlfahrtia magnifica (Diptera: Sarcophagidae).

Cited by 70 publications

References 30 publications

Ignatzschineria indica sp. nov. and Ignatzschineria ureiclastica sp. nov., isolated from adult flesh flies (Diptera: Sarcophagidae)

Ignatzschineria indica sp. nov. and Ignatzschineria ureiclastica sp. nov., isolated from adult flesh flies (Diptera: Sarcophagidae)

A pioneer in the field of autophagy microscopy

Schineria

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