Description of the oöcysts of Eimeria septemvittata n. sp. (Apicomplexa: Eimeriidae) from queen snakes,Regina septemvittata (Serpentes: Colubridae), in Arkansas

Coccidian oöcysts recovered from the feces of queen snakes, Regina septemvittata, from Arkansas, USA, were found to represent a previously unreported eimerian. Oöcysts of Eimeria septemvittata n. sp. are spherical or subspherical, 14.6×14.0 (12–16×12–15) μm, with a thin, bi-layered wall; the shape-index (length/width) is 1.04 (1.00–1.17). The micropyle and oöcyst residuum are absent but a large polar granule is present. The sporocysts are ovoidal, 11.3×5.6 (9.5–13.5×5–6) μm and possess a Stieda body; the shape-index is 2.02 (1.81–2.50). Each sporozoite contains a large, centrally located refractile body and a generally smaller, posterior refractile body.     

Taxonomic status of the extinct Banff longnose dace,Rhinichthys cataractae smithi,of Banff National Park,Alberta

Synopsis Study of 314 specimens of Rhinichthys cataractae from British Columbia, Alberta, and Wyoming, lead to the following conclusions: (1) Rhinichthys cataractae smithi Nichols,1916, is a valid subspecies, endemic to Cave and Basin Hotsprings and distinguished by 48–58 as opposed to 58–74 lateral line scales; (2) between 1925 and 1971, R. c. smithi hybridized with the eastern subspecies R. c. cataractae (Valenciennes,1842) from the Bow River and by 1981 the former had undergone almost complete introgression and was virtually extinct; (3) probable factors leading to this are introduction of tropical fishes into the hotsprings and periodic reduction of inflow from the hotsprings; (4) the closest relative of R. c. smithi is R. c. cataractae, rather than the westslope longnose dace (without a scientific name) inhabiting the Pacific basin; (5) the low number of lateral line scales of R. c. smithi may be a pleomeristic response to dwarfing; (6) R. c. smithi develops breeding tubercles at sizes as small as 21.1 mm SL, whereas R. c. cataractae develop them at 36.3 mm SL in Alberta; (7) introductions should not be made into a body of water prior to the study of its native fishes and consultation with experts in taxonomy and distribution of rare fishes. R. c. smithi is illustrated for the first time.     

Characterization of antimicrobial resistance and seasonal prevalence of Escherichia coli O157:H7 recovered from commercial feedlots in Alberta,Canada

Aims: To characterize antimicrobial resistance (AMR) and determine the seasonal prevalence of Escherichia coli O157:H7 isolated from commercial feedlots. Methods and Results: Escherichia coli O157:H7 were isolated from faecal and oral samples collected at monthly intervals from three commercial feedlots over a 12‐month period. A total of 240 isolates were characterized using pulsed‐field gel electrophoresis (PFGE) technique. A subset of 205 isolates was analysed for AMR using Sensititre system and AMR genes (tet, sul and str) by PCR. Seven PFGE clusters (≥90% Dice similarity) were identified, and two clusters common to all three feedlots were recovered year‐round. The majority of isolates (60%) were susceptible to all antimicrobials and were closely related (P < 0.001), whereas isolates with unique AMR patterns were not related. The prevalences of AMR from feedlots A, B and C were 69%, 1% and 38%, respectively. Resistance to tetracycline (69%) and sulfisoxazole (68%) was more prevalent in feedlot A than other two feedlots. The presence of strA and strB genes was linked in the majority of isolates, and tet(A) and tet(B), and sul1 and sul2 genes were present individually. Escherichia coli O157:H7 were genetically diverse during summer and fall, and strains from winter and spring months were more closely related. Conclusions: Antimicrobial resistance was more common in E. coli O157:H7 obtained from two of the three commercial feedlots, and the phenotypic expression of resistance was correlated with the presence of resistant genes. A highly diverse E. coli O157:H7 population was found during summer and fall seasons. Significance and Impact of the Study: Information would help understanding the dynamics of AMR in E. coli O157:H7 from commercial feedlots.     

Spatially resolved fluorescence correlation spectroscopy using a spinning disk confocal microscope

We develop an extension of fluorescence correlation spectroscopy (FCS) using a spinning disk confocal microscope. This approach can spatially map diffusion coefficients or flow velocities at up to approximately 10(5) independent locations simultaneously. Commercially available cameras with frame rates of 1000 Hz allow FCS measurements of systems with diffusion coefficients D~10(-7) cm(2)/s or smaller. This speed is adequate to measure small microspheres (200-nm diameter) diffusing in water, or hindered diffusion of macromolecules in complex media (e.g., tumors, cell nuclei, or the extracellular matrix). There have been a number of recent extensions to FCS based on laser scanning microscopy. Spinning disk confocal microscopy, however, has the potential for significantly higher speed at high spatial resolution. We show how to account for a pixel size effect encountered with spinning disk confocal FCS that is not present in standard or scanning FCS, and we introduce a new method to correct for photobleaching. Finally, we apply spinning disk confocal FCS to microspheres diffusing in Type I collagen, which show complex spatially varying diffusion caused by hydrodynamic and steric interactions with the collagen matrix.