Hematozoa and a new haemoproteid species from Cathartidae (New World vulture) in South Carolina

A survey of turkey vultures (Cathartes aura) in South Carolina revealed the presence of a novel haemoproteid. Haemoproteus catharti n. sp. is described from the slides developed from the blood of this vulture. The new species is a thick, halteridial form with complete margins, and is considered distinct from the other recognized haemoproteids from the diurnal raptors in shape, pigment number, parasite outline, and host-family specificity. While reviewing blood films, a series of unusual immature schizonts of Plasmodium sp. were also observed, and these are illustrated, along with another distinct haemoproteid from old slides of poor quality produced from turkey vulture blood.     

Distribution of the Family Hydropsychidae (Trichoptera) in the Savannah River Basin of North Carolina,South Carolina and Georgia

Hydropsychids were collected along the length of the Savannah River and its headwaters and tributaries. Species distribution was correlated with chemical and physical properties of water, altitude and stream size. Seven genera and 35 species were found among approximately 100,000 specimens collected. Fourteen species divided into three groups on the bases of altitude and stream size preferences. Turbidity, conductivity, temperature, carbonate, nitrate and nitrite increased along the river's course, whereas maximum velocity and dissolved oxygen decreased. For these factors the maximum value tolerated by a species was associated with the species distribution. The genera Hydropsyche and Cheumatopsyche were the most widely distributed. Several species of these two genera had quite large distributional ranges while others had quite restricted ranges.     

In vitro somatic embryogenesis of Texas ebony (Ebenopsis ebano [Berland.] Barneby & J.W. Grimes)

In Vitro Cellular & Developmental Biology - Plant - Texas ebony (Ebenopsis ebano [Berland.] Barneby & J.W. Grimes) is a member of the Fabaceae that is native to Mexico. Its wood has...     

Ecology of aquatic Lepidoptera (Crambidae: Nymphulinae) in South Carolina, USA

An ecological study was conducted in May and June of 1995 and 1996 in South Carolina to determine the factors associated with distributions of aquatic Lepidoptera (Crambidae: Nymphulinae). Larvae were found at 65 lotic and lentic sites in three ecoregions (Piedmont, Sandhills, Coastal Plain). Nine species of aquatic Lepidoptera were collected from 12 species of aquatic vascular macrophytes. One to six plant species were used as hosts, depending on the species of lepidopteran; however, the number of host plants used by a lepidopteran was significantly correlated with the lepidopteran's frequency of occurrence. Significant habitat associations were found for five species. Langessa nomophilalis (Dyar) was found under the widest range of temperature and width and occurred in both lotic and lentic habitats. Munroessa icciusalis (Walker) was found in lotic and lentic habitats and had the widest range of recorded depths. Parapoynx maculalis (Clemens) occurred at stream sites with lentic-like conditions. Parapoynx obscuralis (Grote) occupied the widest range of pH and was restricted to lotic habitats, and P. seminealis (Walker) was found in both lotic and lentic habitats. Additional species, collected at fewer than 8% of sites, included M. gyralis, P. allionealis, Synclita obliteralis, and S. tinealis. Overall, the distributions of aquatic Lepidoptera in South Carolina were nonrandom and predictable on the basis of habitat characteristics. This revised version was published online in July 2006 with corrections to the Cover Date.     

Roles of tidal and wind-generated currents in transporting white shrimp (Penaeus setiferus) postlarvae through a South Carolina (USA) inlet

The temporal and spatial abundance of postlarval Penaeus setiferuswas studied from plankton samples in oceanic and estuarine watersnear the North Edisto Inlet, South Carolina (USA), during threecruises in 1993 and 1994 (May 1993, August/September 1993 andJune 1994). Each covered a full cycle of neap-spring tides.On each cruise, bongo nets were towed at three stations acrossthe inlet throat on nightly flood tides. During the first twocruises, tows were made at surface and near-bottom depths inthe inlet, while sampling was confined to surface depths duringthe last cruise. Plankton tows were also made outside the inletalong transects extending in a cross-shelf direction and alongan arcuate transect around the inlet mouth. Stations along thearcuate transect were intensively sampled over a full tidalcycle during the last cruise. Extensive oceanographic and meteorologicalobservations were obtained from moored instrument arrays andshipboard sampling in order to relate fluctuations in tidal,lunar and wind phenomena to temporal changes in postlarval density.Densities of postlarvae were greater in the inlet throat thanat stations offshore. A significant interaction of postlarvaldensity among inlet stations and depth was noted in May. Forother cruises, no significant differences in density were notedamong stations across the inlet, but postlarvae were concentratedat the surface. The lack of a consistent horizontal salinitygradient and obvious pattern in water masses across the inletmay explain why postlarval densities did not consistently differlaterally in the inlet. Greater densities generally occurredduring the first quarter moon, although a clear relationshipof larval density to the spring-neap cycle was not observed.Highest mean densities of ingressing postlarvae in surface floodtide collections from the inlet were generally associated withdownwelling onshore winds which generate onshore flow near thesurface. The similarity between the time series curves of postlarvaldensity and the tidal component of currents just offshore ofthe inlet suggests that tidal transport may facilitate movementinto the estuary. Based on increased postlarval density at thesurface during early strong flood tides and a reduced densityat depth in the inlet, we hypothesize that postlarval P setiferusare utilizing selective tidal stream transport.     

A revised key to Stenhelia (Delavalia) (Copepoda: Harpacticoida) including a new species from South Carolina, U.S.A.

A new and unique harpacticoid copepod from Spartina altemiflora salt marshes of the southeastern coast of the United States is described. Stenhelia bifidia sp. nov., differs from its closest allies in having bifid P₅ setae, reduced number of setae on the swimming legs, reduced length of the mandibular enpododite setae and a sexually dimorphic rostrum.
A table listing the salient morphological features of Stenhelia (Delavalia) is given as a new key to the subgenus along with a discussion on the validity of the Stenhelia related genus Me lima Por.     

Treatment of W. bancrofti (Wb) in HIV/Wb Coinfections in South India

BackgroundThe disease course of human immunodeficiency virus (HIV) is often altered by existing or newly acquired coincident infections.Conclusions/SignificanceWe were unable to find a significant effect of W. bancrofti infection or its treatment on HIV clinical course or surrogate markers of HIV disease progression though we recognized that our study was limited by the smaller than predicted sample size and by the use of ART in half of the patients. Treatment of W. bancrofti coinfection in HIV positive subjects (as is usual in mass drug administration campaigns) did not represent an increased risk to the subjects, and should therefore be considered for PLWHA living in W. bancrofti endemic areas.

Trial Registration

ClinicalTrials.gov {"type":"clinical-trial","attrs":{"text":"NCT00344279","term_id":"NCT00344279"}}NCT00344279     

NMR conformational analyses on (des-bromo) neuropeptide B [1-23] and neuropeptide W [1-23]: the importance of alpha-helices, a cation-pi interaction and a beta-turn

The preferred conformations of the orphan G-protein coupled receptor agonists (des-bromo) neuropeptide B [1-23] and neuropeptide W [1-23], referred to as NPB and NPW, have been determined by (1)H NMR, CD, and molecular modeling. The sequences of NPB and NPW are WYKPAAGHSSYSVGRAAGLLSGL and WYKHVASPRYHTVGRAAGLLMGL, respectively. These are hypothalamic peptides that exert their biological actions on GPR7 and GPR8 receptors. Micellar solutions using the membrane mimetic, sodium dodecylsulphate-d(25) (SDS), were used to mimic a physiological environment for the peptides. The secondary structure of NPB consists of a type II beta-turn involving residues Lys(3) to Ala(6). The C-terminal region of NPB exists in a conformational equilibrium between different secondary structures, including an alpha-helix from residues Arg(15) to Ser(21), and a 3(10)-helix from residues Ser(12) to Ser(21). The N-terminus of NPW exhibits a cation-pi interaction between the Lys(3) side chain and the quadrupole moment of the Trp(1) indole group. At the C-terminus of NPW, a well-defined alpha-helical conformation exists from Arg(15) to Met(21). As NPB and NPW have 91% sequence homology from residues Val(13) to Leu(23), with only residue 21 differing between the two peptides, the similar C-terminal secondary structures of these two peptides are consistent with the sequences. This is supported by the similar CD spectra. The different secondary structures at the N-termini for NPB and NPW point to the importance of the N-terminus in receptor binding. This is consistent with the work of Fujii et al. [J. Biol. Chem. 277, 34010-34016 (2002)] who observed that iodination of the NPB Tyr(2) resulted in decreased agonistic activity at GPR7. In addition, Tanaka et al. [Proc. Natl. Acad. Sci. USA 100, 6251-6256 (2003)] showed that deletion of Trp(1) from NPB or NPW drastically decreased activity at GPR7 for NPB and GPR7 and GPR8 for NPW. Therefore, we postulate that the N-terminus is involved in membrane recognition and receptor binding.     

Toxicity of Karlodinium micrum (Dinophyceae) associated with a fish kill in a South Carolina brackish retention pond

A dinoflagellate bloom was found associated with a fish kill event in a South Carolina brackish water retention pond. A multi-analytical approach was used to confirm the identity of the bloom dinoflagellate and evaluate its potential toxicity. Karlodinium micrum was confirmed through light microscopy, pigment profile comparisons, species-specific PCR, and gene sequence data. Necropsy findings on several fish were suggestive of an acute kill event. Toxicity of filtrate from bloom samples was tested by a hemolytic assay using rainbow trout (Oncorhynchus mykis) erythrocytes and an ichthyotoxicity assay using larval zebrafish (Danio rerio). Hemolytic activity was measurably high (>80% hemolysis) in both whole filtrate and fractionated filtrate (from the 80% MeOH C₁₈ column elution). This fraction also demonstrated high ichthyotoxic activity as exposed fish experienced rapid death. These results implicate toxic K. micrum as a causative factor in fish death in a non-aquaculture brackish pond associated with a housing development, and extend recent findings linking this species to fish kills in aquaculture ponds.     

Description of Hemicaloosia graminis n. sp. (Nematoda: Caloosiidae) Associated with Turfgrasses in North and South Carolina,USA

A new nematode species was discovered during a diversity survey of plant-parasitic nematodes on turfgrass conducted in North and South Carolina in 2010 and 2011. It is described herein as Hemicaloosia graminis n. sp. and is characterized by two annuli in the lip region, one lateral line, body 610.0–805.0 μm long, stylet 65.0–74.6 μm long, vulva at 84.1% –85.8% of the body , 254–283 annuli, vulva at the 38–53^rd annulus from tail terminus, 12–14 annuli between vulva and anus, tail elongate-pointed, 67.5–84.8 μm long in females and spicule straight, 31.0 μm long, caudal alae well developed, two lateral lines in males. The newly described species is morphologically closest to H. paradoxa, but has a longer stylet (65.0–74.6 vs 61.0–65.0 μm) and a higher V-value (84.1–85.8 vs 78.1–84.0%), less RV (38–53 vs 50–56), higher RVan (12–14 vs 10) in females, and a shorter tail (30.1 vs 36.7 μm) and more anteriorly located excretory pore (105.9 vs 140.0 μm) in the male. It was easily differentiated from other species based on near-full-length small subunit rRNA gene (SSU) and ITS1 sequences. Phylogenetic analysis from SSU supports placement in a monophyletic clade with the genus Caloosia. An identification key and a table of distinguishing characteristics are presented for all seven species of Hemicaloosia.     

Embryogenesis and haploid induction using anther culture in lovage (Levisticum officinale W.D.J. Koch)

An efficient and robust protocol to induce embryogenesis in lovage (Levisticum officinale W.D.J. Koch) has been developed. Immature anthers, with most of the microspores at the late uninucleate stage, were used as explants, and embryogenesis was induced in medium with combinations of plant growth regulators including α-naphthalene acetic acid (NAA), 2,4-dichlorophenoxyacetic acid (2,4-D), and 6-benzylaminopurine (BAP). The frequencies of in vitro embryogenesis ranged from 0.42 to 18.25% depending on the combinations of plant growth regulators in the induction medium. Induced globular embryos successfully developed into heart and torpedo-staged embryos. Fresh anther explants produced the highest embryo formation rate (17.75%). Anthers treated at 4?ºC for 3, 5, or 8 d, significantly reduced the embryogenic response (to 3.52–7.85%). More embryos were induced when the sucrose content in the medium was increased from 3 to 6% (w/v), but significantly fewer embryos were produced when sucrose was 8% or more. Nearly 20% of fresh anthers were able to produce embryogenic structures when cultured on Murashige and Skoog medium supplemented with 10.74 μM NAA, 8.80 μM BAP, 9.05 μM 2,4-D, and 6% sucrose. Furthermore, when silver nitrate was added to the embryo induction medium at 90 μM, the frequency of anther browning decreased by 30% and the embryo formation rate increased to 24.75% of anthers cultured. In total, 418 plants were regenerated and cytological analysis confirmed 11 haploid lines from 187 samples randomly selected.