Search PubMed⌕ Search

SEARCH · Search PubMed

Results for “Spiroplasma”

Search indexed PubMed citations on genomics, clinical trials, systematic reviews and public health. Explore titles, authors and supplied subject terms, then open the PubMed record.

Quote a phrase for an exact phrase match. Source license links do not imply unrestricted reuse.

At least 55 records · Page 3Linked to original sources

Spiroplasma fibrils.

A fundamental question in biology concerns the morphology of spiroplasmas: How does a wall-less microorganism maintain its characteristic morphology as a helical filament? An answer to this question began to form when it was discovered that spiroplasmas treated with any of a number of detergents (sodium deoxycholate, Triton X-100, Nonidet P-40) release their cytoplasmic contents. If this procedure is performed on a formvar-coated electron microscope grid and the resultant preparation negatively stained and observed by transmission electron microscopy, numerous striated microfibrils can be seen where spiroplasmas once were. The fibrils are of varying lengths, 4 nm in width, and show a striation repeat at 9 nm along their length. It is not possible to discern from the pattern of the released fibrils just how they are organized within the intact spiroplasma; nor is it yet possible to identify a fibrillar substructure in thin sections or in freeze-fractured organisms. Townsend and his colleagues at the John Innes Institute in Norwich, UK, purified fibrils by density gradient centrifugation. SDS-PAGE showed the fibrils to consist of a 55,000-dalton protein recognizable in the four serogroups tested by protein blotting with an antiserum made against the PAGE-separated protein. The presence of fibrils is a feature common to all spiroplasma, regardless of whether they are helical or nonhelical, as in the Ixodes tick-derived spiroplasma or Townsend's ASP-1 strain of Spiroplasma citri. We have employed gentle demembranation treatments that preserve filamentous substructure in an effort to elucidate the organization of the fibrils within the spiroplasma cell.

Bacterial Proteins↗

Temperature Ranges, Growth Optima, and Growth Rates of Spiroplasma (Spiroplasmataceae, class Mollicutes) Species

A new method was developed for determination of the doubling times of spiroplasmas. In this procedure, the time required for medium acidification of tubes in tenfold dilution series was recorded. Sixty-four spiroplasma strains, representing 24 groups and 11 subgroups, were studied. Eight strains representing putative new groups were also included in the study. Doubling times at 5, 10, 15, 20, 25, 30, 32, 37, 41, and 43°C were determined. The range of temperatures for spiroplasma growth was 5°-41°C. Twenty-three spiroplasmas had optima of 30°C, 29 had optima of 32°C, and 13 had optima of 37°C. The fastest growing spiroplasma was the MQ-4 strain (group XI), with a doubling time at optimal temperature of 0.6 h. The slowest was the Jamaican corn stunt strain B655 (subgroup I-3), with an optimal doubling time of 36.7 h. Spiroplasma strain B31 (group IV) had the widest range (5°-41°C), while the DW-1 strain and some subgroup I-3 strains had the narrowest, growing only at 25° and 30°C. Some spiroplasmas grew well at 41°C, but none grew at 43°C. The ability of spiroplasmas to withstand a wide range of temperatures may reflect the conditions to which they are exposed in nature, including the temperatures of the insect, tick, and/or plant hosts in which they are carried and the plant surfaces from which they may be acquired by arthropods.

Journal Article↗

Morphology of spiroplasmas in the Chinese mitten crab Eriocheir sinensis associated with tremor disease.

The structure of spiroplasmas in the Chinese mitten crab associated with tremor disease was studied by transmission electron microscopy techniques, including both negative staining and ultrasectioning. A spiral structure, which is a typical form of spiroplasmas, could be detected and the observations showed for the first time the presence of spiroplasmas in the cells of the crab. Propagation of spiroplasmas within the cells presented various forms that could be sorted into three morphological types: rounded, regular helical, and pleiomorphic or intermediate forms. The spiroplasmas appeared as round bodies during the fallow stage of development or under poor conditions. They showed various shapes such as helices, saccate, branched, tadpole-like and tortoise-like structures while growing, and became long and congregated in late stages of development. When spiroplasmas were isolated from chicken eggs and cultured in M1D medium they appeared to undergo similar morphological changes to those in the crab. The spiroplasmas contained chromatin filaments and peripheral ribosome-like granules and were delimited by distinct unitary membranes. Average diameters were calculated at 0.1 to 0.35 microm for rounded forms and 0.1-0.2 microm for helical or long forms, and they varied in length from 3-12 microm.

Animals↗

Spiroplasma diminutum sp. nov., from Culex annulus mosquitoes collected in Taiwan.

Initially, strain CUAS-1T (T = type strain), which was isolated from a frozen triturate of Culex annulus mosquitoes collected in Taiwan, was thought to be a member of spiroplasma group VII. This placement was based on the spiroplasma deformation test titer observed when strain CUAS-1T spiroplasmas were tested with Spiroplasma monobiae MQ-1T antiserum. The results of subsequent reciprocal spiroplasma deformation, metabolism inhibition, and growth inhibition tests clearly revealed that strain CUAS-1T is not serologically related to previously described spiroplasma groups (groups I to XXIV) and thus is a representative of a new group, group XXV. Strain CUAS-1T was characterized by using the minimal standards for mollicute species descriptions. During logarithmic-phase growth, strain CUAS-1T cells are characteristically very short helices with 1.5 to 2 helical turns (1 to 2 microns), highly motile, and bounded by a single trilaminar membrane and form granular colonies with satellites when the organism is grown aerobically on MID medium containing 1.6% agar. Growth in MID broth occurs at temperatures ranging from 10 to 37 degrees C, and the optimum temperature is 30 degrees C. Substrate utilization tests revealed that cholesterol is required for growth, that glucose is hydrolyzed, and that arginine is not hydrolyzed both in the presence and in the absence of glucose. The genome of strain CUAS-1T is 1,080 kbp long, and the guanine-plus-cytosine content is 26 +/- 1 mol%. On the basis of the results of our studies we propose that strain CUAS-1T (group XXV) should be placed in a new species, Spiroplasma diminutum. Strain CUAS-1 (= ATCC 49235) is the type strain of S. diminutum.

Animals↗

Mosquito spiroplasmas from France and their ecology.

Spiroplasmas have been isolated previously from a number of blood-sucking arthropods, including ticks, horseflies, and deerflies. More recently, spiroplasmas were isolated from mosquitoes from the USA, France, and Taiwan. Spiroplasmas isolated from mosquitoes from France belong to at least three serogroups and are serologically different from one of the Taiwan isolates, Sp2. Our Ar 1343 strain is the prototype of a new serogroup (XIII). During 3 consecutive years (1983-85), the ecology of these spiroplasmas was studied in different biotopes near, and in, the Isère River Valley in Savoia, France. A total of 23 strains was isolated from four species or groups of mosquitoes (Aedes sticticus/vexans, Ae. cantans/annulipes, Ae. cinereus/geminus and Coquillettidia richiardii). Spiroplasmas were isolated only from female mosquitoes and only during June and July. An as yet unidentified virus was also isolated from three mosquito pools, one of which yielded spiroplasmas. Spiroplasma viruses were not detected. Antibody to our Ar 1357 isolate was found in 4 of 20 sera from cows living in the areas studied, but not in sera from wild rodents or in sera from rabbit or pigeon sentinels. Finally, preliminary results are presented on the effects of experimental infection of Ae. aegypti with the Ar 1357 isolated (serogroup XXII).

Animals↗

Spiroplasma plasmids.

Extrachromosomal DNA, constituting plasmids or replicative forms of viruses, has been detected in a variety of spiroplasmas, particularly in Spiroplasma citri. Only a few of the S. citri plasmids were characterized by restriction enzyme mapping, and essentially nothing is known on functions encoded by the plasmids. Our studies revealed in S. citri (R8A2) an 8.0-kbp plasmid that differed from previously described plasmids in its restriction map. It was also clonable in pBR322. The plasmid, named pRA1, was found in large quantities as free plasmid in S. citri (R8A2) subclones of low passage level. In subclones of higher passage levels, free plasmid was replaced by plasmid sequences integrated into the spiroplasma chromosome, as revealed by Southern hybridization blots of digested spiroplasmal DNA with nick-translated pRA1 or its recombinant as probes. Significant quantities of integrated plasmid sequences were also observed in S. kunkelii and in Spiroplasma sp. P40. Small quantities of free and/or integrated plasmid DNA were detected in some spiroplasmas serologically and genotypically remote from S. citri. Chromosome-integrated pRA1 sequences were cloned into the Escherichia coli plasmids pUC13 and M13. Hybridization tests and restriction maps of these clones indicated that the integrated plasmid sequences consisted of small repetitive sequences inserted into specific sites on the spiroplasma chromosome. Despite the large number of the inserts they do not appear to affect significantly gene expression in the spiroplasma. Due to the abundance of free and integrated pRA1 in S. citri, nick-translated pRA1 was effective as a DNA probe in detecting small numbers of S. citri in infected periwinkle plants and leafhoppers.

Cloning, Molecular↗

SpV3 viruses of Drosophila spiroplasmas.

The presence of spiroplasmas in the hemolymph of four Drosophila willistoni group species has been shown to cause elimination of males from the progeny of infected females. These spiroplasmas, known as sex-ratio organisms (SROs), are found in D. equinoxialis (ESRO), D. nebulosa (NSRO), D. paulistorum (PSRO), and D. willistoni (WSRO). In addition, a nonmale-lethal spiroplasma (HIS) has been found in the hemolymph of D. hydei. Only the WSRO has been cultivated. Each of the Drosophila spiroplasmas sheds at least one endogenous virus into the hemolymph by a budding process. These viruses are short-tailed polyhedrons resembling the SpV3 virus of Spiroplasma citri, and all have been shown to lyse at least one other strain of SRO. The Drosophila spiroplasma viruses have been extracted from infected flies and purified by metrizamide gradient centrifugation. The viruses, thus purified, maintained infectivity and lysed indicator strains of SROs. Electrophoresis of viral DNA produced bands indicating genomes of three different sizes: 17, 21.8, and greater than 30 kbp. Some SRO strains have more than one SpV3 virus. Restriction endonuclease digestion of DNA of the spiroplasma viruses HSV and NSV (both 21.8 kbp) produce patterns on agarose gels that indicate linear, circularly permuted genomes. The fragments generated by cleavage of NSV with EcoRI have been cloned into pBR325 and amplified in Escherichia coli. Restriction endonuclease digestion of NSV DNA hybridized with these clones indicates that there are two different 21.8-kbp SpV3 viruses in NSRO.

Animals↗

Neuropathology of spiroplasma infection in the rat brain.

This study was designed to demonstrate the neuropathology of persistent spiroplasma infection in the rat brain. GT-48 spiroplasmas were inoculated intracranially into a series of suckling Sprague-Dawley rats. Their brains were evaluated at specific time intervals by microbiologic assay and by morphologic studies including histology, electron microscopy, and immunocytochemistry. The spiroplasmas were observed in the tissues by electron microscopy at peak infection 14 days after intracranial inoculation. At that time they were seen in vacuoles and neuronal processes within the neuropil as filamentous or bleb-like forms. A single tight spiral was identified that closely resembled the spiroplasma-like inclusions previously reported in Creutzfeldt-Jakob disease. The spiroplasmas were shown to spread rapidly throughout the brain tissues presumably by intraneuronal transport. In specimens examined at 25 days after intracranial inoculation and beyond, organisms were localized to gray matter without inflammatory response. The spiroplasmas could not be identified by electron microscopy in the rat brain tissue at late stages of infection. This study has shown an unusual adaptation of spiroplasma infection to the mammalian host brain tissues.

Animals↗

Discovery of a new plant-pathogenic spiroplasma.

To study natural transmission of Spiroplasma citri in the Mediterranean area, periwinkles (Vinca rosea L.) were exposed to natural infection in several locations during the summer of 1983. Detection of S. citri in the periwinkles was assayed by ELISA and culture of the organisms. Some of the periwinkles developed yellows disease symptoms; they contained helical organisms in their sieve tubes, as determined by electron microscopy. A spiroplasma could be cultured from them, but their ELISA reaction for S. citri detection was negative. These results suggested that a spiroplasma different from S. citri had been discovered. The apparently new spiroplasma (P40) was examined for serological relationships with other spiroplasmas by metabolism inhibition and deformation tests. Spiroplasma P40 was found to have relatedness only to Group I spiroplasmas. Healthy periwinkles graft inoculated with shoots of the initial symptomatic periwinkle showed yellows symptoms 3 months after inoculation. Extracts of the initial and the graft-inoculated periwinkles gave positive ELISA reactions with anti-P40 IgG.

Base Composition↗

Bilirubin incorporation into spiroplasma membranes and methylation of spiroplasmal DNA.

Spiroplasma floricola (BNR-1), Spiroplasma sp. MQ-1 and S. apis (B-31) grown in media containing horse serum exhibited intense yellow pigmentation. Yellow pigments were not observed in S. citri (R8A2) and Spiroplasma sp. strains BC-3 and PPS-1 grown in the same medium. The reddish-yellow pigment showed up in lipid extracts of both spiroplasma membranes and horse serum. It exhibited the typical features of bilirubin: specific absorption spectrum from 390 to 500 nm with a peak at 453 nm, and a characteristic sequence of color changes on addition of HNO3 to its solution in chloroform. The pigment comigrated with commercial bilirubin from bull gall and stained greenish blue when subjected to mild oxidation by iodine. S. floricola contained 5.4 micrograms bilirubin/mg cell protein or 9.7 micrograms bilirubin/mg membrane protein. High-performance liquid chromatography (HPLC) showed the presence of significant amounts of 5-methylcytosine and very little 6-methyladenine in the DNA of S. floricola, S. apis and Spiroplasma sp. strains PPS-1 and MQ-1. S. citri and Spiroplasma sp. strain BC-3 contained 6-methyladenine and very little, if any, 5-methylcytosine. The methylated cytosine residues in Spiroplasma sp. MQ-1 were almost exclusively located in the sequence CpG, as in eukaryotes.

5-Methylcytosine↗

Spiroplasma species share common DNA sequences among their viruses, plasmids and genomes.

Alkaline-Southern-blot analyses showed that a spiroplasma plasmid, pRA1, obtained from Spiroplasma citri (Maroc-R8A2), contained DNA sequences that were homologous to spiroplasma type 3 viruses (SV3) obtained from S. citri (Maroc-R8A2), S. citri (608) and S. mirum (SMCA). In addition, pRA1 and SV3(608) DNA shared common, but not necessarily related, sequences with extrachromosomal DNA derived from 11 Spiroplasma species or strains. Furthermore, SV3(608) had DNA homology with the chromosome from 6 distinct spiroplasmas but not with chromosomal DNA from eight other Spiroplasma species or strains. The biological function of these common sequences is unknown.

Bacteriophages↗

A novel Spiroplasma pathogen causing systemic infection in the crayfish Procambarus clarkii (Crustacea: Decapod), in China.

A novel disease of crayfish Procambarus clarkii appeared in the summer of 2004 in freshwater aquaculture in Jiangsu province of China. Light and transmission electron microscopy (TEM), molecular biological methods and in vitro culture were used to identify the pathogen. The agent was unique in having a helical morphology and rotary motility as observed by phase-contrast light microscopy and was found in haemolymph, muscles, nerves and connective tissues by smear method and TEM. Ultra-thin sections under TEM revealed the wall-free membrane of the microbe. The agent could pass through membrane filters with pores 220 nm in diameter and was cultivated in vitro in M1D medium. 16S rDNA of the crayfish pathogen was amplified by PCR using primers specific for Spiroplasma-specific 16S rDNA. The resultant 271bp PCR product showed 99% identity with Spiroplasma mirum 16S rDNA, having a close relationship with the spiroplasma from the Chinese mitten crab Eriocheir sinensis. This is the second time a spiroplasma has been found in a freshwater crustacean. The 271bp PCR product was also amplified from the bottom mud in the ponds associated with the disease. The PCR molecular method is an effective way to detect spiroplasma in freshwater environment. The results from this study are significant in expanding the host range of spiroplasma and freshwater ecology.

Animals↗

Characterization of spiroplasmas by serology.

Five major serologic groups of spiroplasmas have been distinguished on the basis of serology (as determined in a test of deformation and metabolism inhibition), guanine-plus-cytosine content of DNA, and DNA-DNA hybridization. group I includes strains of Spiroplasma citri that form a classical subgroup (serovar) complex of four serologically homogeneous serovars that cross-react with each other at varying levels. The four other serogroups do not cross-react with each other or with members of the group I S. citri complex. Group II consists of the sex ratio spiroplasma from Drosophila species. Group III contains spiroplasmas isolated from flowers of magnolia and tulip trees. Group IV consists of strains of spiroplasmas recovered from insects and flowers. The tick-derived spiroplasmas SMCA and TP-2 compose group V.

Cytosine↗

Spiroplasma sp. 16S rDNA in Creutzfeldt-Jakob disease and scrapie as shown by PCR and DNA sequence analysis.

The pathogenesis of the transmissible spongiform encephalopathies (TSE), which include Creutzfeldt-Jakob disease (CJD) in humans and scrapie in sheep, remains an enigma. In this paper we present evidence for the association of Spiroplasma sp., a wall-less prokaryote, with TSE. We have shown PCR amplification of Spiroplasma 16S rDNA in TSE-infected brain tissues (13 of 13 CJD cases and 5 of 9 scrapie cases) and not in control brains (0 of 50). Direct sequencing of the amplified PCR products has confirmed the presence of Spiroplasma-like DNA in all 5 of the TSE brains tested. Our evidence is not necessarily in conflict with involvement of a PrPres--a protease-resistant host-derived protein referred to as the prion--in the pathogenesis of TSE, since there is evidence that another factor is involved. We propose a bacterium, namely Spiroplasma, as this associated factor although the role of Spiroplasma in TSE cannot be determined from these experiments. The presence of the nucleic acid sequence of this microbe in all cases of TSE in our laboratory and not in controls provides direct evidence of the association of Spiroplasma sp. with TSE.

Animals↗

Spiroplasma diabroticae sp. nov., from the southern corn rootworm beetle, Diabrotica undecimpunctata (Coleoptera:Chrysomelidae).

Spiroplasma strain DU-1T (T = type strain), which was isolated from hemolymph of the corn rootworm Diabrotica undecimpunctata (Coleoptera:Chrysomelidae), was serologically distinct from other spiroplasma species, groups, and subgroups. Cells of strain DU-1T were shown by light microscopy to be helical motile filaments. Electron microscopy revealed cells bounded by a single cytoplasmic membrane, with no evidence of a cell wall. The organism was not sensitive to 500 U of penicillin per ml. Strain DU-1T grew well in SM-1, M1D, and SP-4 liquid media, in broth supplemented with 1% bovine serum fraction or conventional horse serum, and under both aerobic and anaerobic conditions. This organism did not appear to have a sterol requirement for growth, as has been reported for several other Spiroplasma species or strains. Optimal growth occurred at 32 degrees C, with a doubling time of 0.9 h; strain DU-1T multiplied at 10 to 41 degrees C but failed to grow at 5 or 43 degrees C. It produced acid from glucose but hydrolyzed neither arginine nor urea. The results of reciprocal serologic tests in which antigens or antisera to established Spiroplasma species, groups, subgroups, and putative groups were used indicated that strain DU-1T was serologically distinct. This organism has a DNA guanine-plus-cytosine content of 25 +/- 1 mol% and a genome size of 1,350 kbp. Strain DU-1T is a member of a cluster of fast-growing insect-associated spiroplasmas, as determined by sequence analysis of 16S rRNA. On the basis of the results of this study and previously published data, strain DU-1 (= ATCC 43210) is designated the type strain of a new species, Spiroplasma diabroticae.

Animals↗

Spiroplasma leucomae sp. nov., isolated in Poland from white satin moth (Leucoma salicis L.) larvae.

Spiroplasma sp. strain SMA(T), isolated in Poland from white satin moth larvae, Leucoma salicis L. (Lepidoptera: Lymantriidae), was serologically distinct from other Spiroplasma species, groups or subgroups. Dark-field microscopy of the cells revealed the classical helical shape and subsequent transmission electron microscopy revealed cells surrounded by only a single cell membrane (lacking a cell wall). Growth of strain SMA(T) occurred in M1D medium at 30 degrees C. Strain SMA(T) catabolized both glucose and arginine, but did not hydrolyse urea. The G+C content of the DNA was 24+/-1 mol% as determined by melting temperature analysis. Serological analysis revealed a very weak cross-reactivity (positive reaction only up to a 1 : 80 dilution) with two Spiroplasma strains, 277F (Spiroplasma sp. group I-4) and LB-12 (Spiroplasma sp. group I-5). Strain SMA(T) (=ATCC BAA-521T=NBRC 100392T) is designated the type strain of a novel species, Spiroplasma leucomae sp. nov. (class Mollicutes: order Entomoplasmatales: family Spiroplasmataceae).

Animals↗

Spiroplasmas: cultivation in chemically defined medium.

A chemically defined medium, CC-494, supports the cultivation in vitro of several spiroplasmas belonging to three distinct serogroups. Medium CC-494 supports the growth of flower spiroplasmas FS 23-6 and FS SR-3 and of honey bee spiroplasma HBS AS-576. The maximal populations of the two flower spiroplasmas and honey bee spiroplasma are comparable to those cultured in the undefined medium C-3G. The growth rate for all three spiroplasmas is slower in the defined medium.

Culture Media↗

Population dynamics of male-killing and non-male-killing spiroplasmas in Drosophila melanogaster.

The endosymbiotic bacteria Spiroplasma spp. are vertically transmitted through female hosts and are known to cause selective death of male offspring in insects. One strain of spiroplasma, NSRO, causes male killing in Drosophila species, and a non-male-killing variant of NSRO, designated NSRO-A, has been isolated. It is not known why NSRO-A does not kill males. In an attempt to understand the mechanism of male killing, we investigated the population dynamics of NSRO and NSRO-A throughout the developmental course of the laboratory host Drosophila melanogaster by using a quantitative PCR technique. In the early development of the host insect, the titers of NSRO were significantly higher than those of NSRO-A at the first- and second-instar stages, whereas at the egg, third-instar, and pupal stages, the titers of the two spiroplasmas were almost the same. Upon adult emergence, the titers of the two spiroplasmas were similar, around 2 x 10(8) dnaA copy equivalents. However, throughout host aging, the two spiroplasmas showed strikingly different population growth patterns. The titers of NSRO increased exponentially for 3 weeks, attained a peak value of around 4 x 10(9) dnaA copy equivalents per insect, and then decreased. In contrast, the titers of NSRO-A were almost constant throughout the adult portion of the life cycle. In adult females, consequently, the titer of NSRO was significantly higher than the titer of NSRO-A except for a short period just after emergence. Although infection of adult females with NSRO resulted in almost 100% male killing, production of some male offspring was observed within 4 days after emergence when the titers of NSRO were as low as those of NSRO-A. Based on these results, we proposed a threshold density hypothesis for the expression of male killing caused by the spiroplasma. The extents of the bottleneck in the vertical transmission through host generations were estimated to be 5 x 10(-5) for NSRO and 3 x 10(-4) for NSRO-A.

Animals↗