Genetic investigation of equine recurrent uveitis in Appaloosa horses

Equine recurrent uveitis (ERU) is characterized by intraocular inflammation that often leads to blindness in horses. Appaloosas are more likely than any other breed to develop insidious ERU, distinguished by low-grade chronic intraocular inflammation, suggesting a genetic predisposition. Appaloosas are known for their white coat spotting patterns caused by the leopard complex spotting allele (LP) and the modifier PATN1. A marker linked to LP on ECA1 and markers near MHC on ECA20 were previously associated with increased ERU risk. This study aims to further investigate these loci and identify additional genetic risk factors. A GWAS was performed using the Illumina Equine SNP70 BeadChip in 91 horses. Additive mixed model approaches were used to correct for relatedness. Although they do not reach a strict Bonferroni genome-wide significance threshold, two SNPs on ECA1 and one SNP each on ECA12 and ECA29 were among the highest ranking SNPs and thus warranted further analysis (P = 1.20 × 10⁻⁵, P = 5.91 × 10⁻⁶, P = 4.91 × 10⁻⁵, P = 6.46 × 10⁻⁵). In a second cohort (n = 98), only an association with the LP allele on ECA1 was replicated (P = 5.33 × 10⁻⁵). Modeling disease risk with LP, age and additional depigmentation factors (PATN1 genotype and extent of roaning) supports an additive role for LP and suggests an additive role for PATN1. Genotyping for LP and PATN1 may help predict ERU risk (AUC = 0.83). The functional role of LP and PATN1 in ERU development requires further investigation. Testing samples across breeds with leopard complex spotting patterns and a denser set of markers is warranted to further refine the genetic components of ERU.     

Characterization of the ColE1 mobilization region and its protein products

Summary A third of the 6.6 kb genome of ColE1 is devoted to mobilization (mob) genes necessary to promote its specific transfer in the presence of conjugative plasmids. Themob region is genetically complex: twomob genes are entirely overlapped by a third. Oligonucleotide-directed mutagenesis was used to insert an amber codon into one of the overlapped genes and make possible a full complementation analysis ofmob. Fourmob genes essential for mobilization by R64drd11 were thus identified. Fragments ofmob were subcloned under control of the P_tac promoter in a suitable vector, overexpressed in minicells and the mobilization proteins visualized. A comprehensive alignment of themob region of ColE1 with those of its close relatives ColK and ColA demonstrating that the four essentialmob genes are conserved is also presented.     

Evidence of a microtrabecular cytoskeletal lattice in glandular cells of hydrozoan planulae

Hydrozoan planulae of Pennaria tiarella and Podocoryne carnea were processed for transmission electron microscopy using diethylene glycol distearate (DGD). The DGD functions as a removable embedding medium to produce embedment-free sections of intact planulae. Images of glandular cells obtained using embedment-free sections were compared with those from conventional Spurr-embedded sections. In unembedded sections a large number of thin anastomosing fibers were observed throughout the cytoplasm of the glandular cell. The fibers appeared to coalesce in certain areas to form thick bundles of fibers that partitioned the glandular cytoplasm into spherical compartments. The meshwork of fibers is three-dimensional and resembles a microtrabecular lattice. Mitochondria are suspended within and attached to the network of fibers, thus suggesting a cytoskeletal role of the fibers. This study documents the presence of a cytoplasmic fiber system within cells of intact invertebrate larvae.     

The nature and location of Acholeplasma laidlawii membrane proteins investigated by two-dimensional gel electrophoresis.

The high resolution, two-dimensional electrophoresis system for the separation of proteins described by O'Farrell, (O'Farrell, P.H. (1975) J. Biol. Chem. 250, 4007--4021) has been modified for the separation of Acholeplasma laidlawii proteins. Reproducible protein patterns have been obtained from A. laidlawii cell, membrane and soluble protein preparations. The isoelectric focusing of membrane proteins was greatly improved by removing the bulk of the membrane lipid before solubilizing the protein. A. laidlawii peripheral membrane proteins were removed from the membrane by low ionic strength washing and by treatment with EDTA. The effect of an exhaustive EDTA treatment and a rapid, warm EDTA treatment were compared. By comparing the protein patterns obtained in these ways it was possible to distinguish two separate groups of peripheral membrane proteins and one integral membrane protein group. The peripheral membrane proteins which were removed from the membrane at low ionic strength (group I) were also insoluble in Triton X-100, whereas additional peripheral membrane proteins extractable by subsequent EDTA treatment (group II) were soluble in Triton X-100. Exterior-facing membrane proteins were distinguished from the interior-facing ones by lactoperoxidase-catalyzed iodination of intact cells and membranes. Group I peripheral membrane proteins faced the cell interior whereas group II proteins faced the cell exterior. We counted approximately 320 individual whole cell proteins. Of these, about 140 were membrane associated and a maximum of 40 proteins were iodinated after iodinating intact cells. A. laidlawii was also grown in the presence of NaH232PO4 and whole cell proteins were separated by two-dimensional gel electrophoresis. One membrane protein and two soluble proteins were labelled.     

Behavior of Lambs in Rest Pens During Long-Distance Transport

The aim of this study was to determine how one group of lambs utilized 2 consecutive rest periods in novel environments with access to food and water that occurred during 22 hr of motor transport. The 18.5 ± 0.6 kg lambs (n = 15) were transported for 8 hr and then unloaded for a 6-hr rest period. After 6 hr, the lambs were reloaded for another 8 hr of transport followed by a 24-hr rest period. Reloading for a second 8 hr of transport followed the initial rest period. The percentage of lambs engaged in drinking, eating, lying, playing, or “other” was determined at 15-min intervals. During the 6-hr rest period, peak lying behavior occurred during the 2nd and 6th hr of the period. During the first 6 hr of the 24-hr rest period, the percentage of lambs lying increased while the percentage of lambs eating decreased. In addition, the percentage of lambs lying during the first 6 hr of the 24-hr rest period was greater than during the 6-hr rest period. Lying down had a greater priority than eating during the second (24-hr) rest period.     

Optimisation of an oviposition protocol employing human chorionic and pregnant mare serum gonadotropins in the Barred Frog Mixophyes fasciolatus (Myobatrachidae)

ABSTRACT: BACKGROUND: Protocols for the hormonal induction of ovulation and oviposition are essential tools for managing threatened amphibians with assisted reproduction, but responses vary greatly between species and even broad taxon groups. Consequently, it is necessary to assess effectiveness of such protocols in representative species when new taxa become targets for induction. The threatened genus Mixophyes (family Myobatrachidae) has amongst the highest proportion of endangered species of all the Australian amphibians. This study developed and optimised the induction of oviposition in a non-threatened member of this taxon, the great barred frog (Mixophyes fasciolatus). METHODS: Gravid female M. fasciolatus were induced to oviposit on one or more occasions by administration of human chorionic gonadotropin (hCG) with or without priming with pregnant mare serum gonadotropin (PMSG). Treatments involved variations in hormone doses and combinations (administered via injection into the dorsal lymph sacs), and timing of administration. Pituitary homogenates from an unrelated bufonid species (Rhinella marina) were also examined with hCG. RESULTS: When injected alone, hCG (900 to 1400 IU) induced oviposition. However, priming with two time dependent doses of PMSG (50 IU, 25 IU) increased responses, with lower doses of hCG (200 IU). Priming increased response rates in females from around 30% (hCG alone) to more than 50% (p = 0.035), and up to 67%. Increasing the interval between the first PMSG dose and first hCG dose from 3 to 6 days also produced significant improvement (p<0.001). Heterologous pituitary extracts administered with hCG were no more effective than hCG alone (p = 0.628). CONCLUSIONS: This study found that M. fasciolatus is amongst the few amphibian species (including Xenopus (Silurana) and some bufonids) that respond well to the induction of ovulation utilising mammalian gonadotropins (hCG). The optimal protocol for M. fasciolatus involved two priming doses of PMSG (50 IU and 25 IU) administered at 6 and 4 days respectively, prior to two doses of hCG (100 IU), 24 hours apart. This study is also the first to demonstrate in an amphibian species that responds to mammalian gonadotropins that an increase in the ovulation rate occurs after priming with a gonadotropin (PMSG) with FSH activity.     

Characterisation of an Apparently Novel Soluble Protein Fraction found in Pathogen and Osmotically-stressed Cucumber Cotyledons

Cotyledons of cucumber (Cucumis sativus L. cv. Ashley) were used to study the alterations that occur in the soluble protein fraction following either tobacco necrosis virus-elicited necrosis or a period of mannitol-induced osmotic-stress. One apparently novel fraction (termed γ) was induced in the soluble protein fraction after necrosis or osmotic stress and was identified by disc-PAGE and gel staining. Smaller amounts of the γ fraction were present in apparently healthy tissue adjacent to necrotic halves of cotyledons (AH tissue), but were absent from any other leaves on these plants. The γ fraction is probably representative of at least three different proteins, two of which are constituents of control tissue (a glycoprotein and possibly one or two RNAse isozymes) while the third is a protein of unknown nature, present as the bulk of the γ fraction and possibly synthesized de novo. Following the radio-active labelling of AH tissue it would appear that an increased protein synthesis, which is sensitive to the effects of translational inhibitors may result in the production of the γ fraction, but this is speculative. The major component of the γ fraction gave a single band on SDS PAGE, with an Mr of ca. 22,000 and focussed to a single band at pl 4,1 on IEF. While it is thought the bulk of the novel portion of the γ fraction is represented in these gel systems increased amounts of the constitutive glycoprotein component should be taken into consideration. Soluble extracts of protoplasts isolated from AH tissue retained only constitutional RNAse isozyme(s), and were totally devoid of the rest of the γ fraction. This result suggests that the other component(s) of the γ fraction is (are) subcellularly located in the plasmodesmata, between the cell wall and plasma membrane or non-covalently attached to either.     

Modern tropical analogs for Carboniferous standing forests: Comparison of extinct Mesocalamites with extant Montrichardia

Assemblages of in situ upright stem casts, or fossil standing forests, provide information on the composition and spatial arrangement of the original plant communities they record, with minimal taphonomic bias. Stands of calamites and lycopsids are found repeatedly as fossil forests in the Late Carboniferous, while other major groups of plants are only rarely preserved in this way. The Carboniferous coal measures of Europe and North America were formed in low‐latitude, tropical environments. The ancient plant communities of these settings can be interpreted by comparison of their taxa with specific, modern tropical analogs. Here, ancient standing forests of the extinct sphenopsid Mesocalamites suckowii are compared with modern stands of the monocot Montrichardia arborescens. These modern analogs occur in the Orinoco Delta of Venezuela and the mouth of the Amazon. Montrichardia and its ancient counterparts occur in comparable clastic facies of fluvio‐deltaic and estuarine depositional systems. Although Mesocalamites and Montrichardia are very different anatomically and taxonomically, they exhibit some intriguing morphological similarities that can be linked to a common ecology. These modern and ancient taxa have evolved convergent forms of vegetative propagation that enable the plants to colonize and survive in environments characterized by very high rates of sedimentation, or episodic sedimentation events. Such environments have an unusually high potential to preserve standing forests.