Methicillin-resistant staphylococci amongst veterinary personnel, personnel-owned pets, patients and the hospital environment of two small animal veterinary hospitals.

This study investigated the transmission cycle of methicillin-resistant Staphylococcus aureus (MRSA) and Staphylococcus pseudintermedius (MRSP) in small companion animal veterinary practice. Sampling was undertaken at two small animal veterinary hospitals in Sydney, Australia. Samples were collected from 46 veterinary personnel, 79 personnel-owned dogs and cats, 151 clinically normal canine hospital admissions and 25 environmental sites. Nasal swabs were collected from veterinary personnel. Nasal, oral and perineal swabs were collected from animals. Methicillin resistance was detected by growth on BrillianceTM MRSA 2 Agar and confirmed by cefoxitin and oxacillin broth microdilution for S. aureus and S. pseudintermedius, respectively. MRSA and MRSP isolates were characterised using whole genome sequencing including mecA gene screening and multilocus sequence typing. MRSA was isolated from four (8%) veterinary personnel but no animals. MRSP was isolated from 11/151 (7%) of canine hospital admissions and 4/53 (8%) of personnel-owned dogs but no veterinary personnel or cats. No MRSA or MRSP was isolated from the environment. MRSP isolates were resistant to significantly more antimicrobial classes than MRSA. The main MRSP clone carried by canine patients (ST496) was distinct to that carried by personnel-owned dogs (ST64). One veterinary nurse, who carried Panton Valentine leucocidin-positive ST338 MRSA, also owned a ST749 MRSP-positive dog. Besides MRSP-positive dogs from the same household sharing the same clone of MRSP, MRSA and MRSP were not shared between humans, animals or environment. Therefore, in the non-outbreak setting of this study, there was limited MRS transmission between veterinary personnel, their pets, patients or the veterinary environment.

Three-Dimensional Growth of Li2S in Lithium-Sulfur Batteries Promoted by a Redox Mediator.

During the discharge of a lithium-sulfur (Li-S) battery, an electronically insulating 2D layer of Li2S is electrodeposited onto the current collector. Once the current collector is enveloped, the overpotential of the cell increases, and its discharge is arrested, often before reaching the full capacity of the active material. Guided by a new computational platform known as the Electrolyte Genome, we advance and apply benzo[ghi]peryleneimide (BPI) as a redox mediator for the reduction of dissolved polysulfides to Li2S. With BPI present, we show that it is now possible to electrodeposit Li2S as porous, 3D deposits onto carbon current collectors during cell discharge. As a result, sulfur utilization improved 220% due to a 6-fold increase in Li2S formation. To understand the growth mechanism, electrodeposition of Li2S was carried out under both galvanostatic and potentiostatic control. The observed kinetics under potentiostatic control were modeled using modified Avrami phase transformation kinetics, which showed that BPI slows the impingement of insulating Li2S islands on carbon. Conceptually, the pairing of conductive carbons with BPI can be viewed as a vascular approach to the design of current collectors for energy storage devices: here, conductive carbon "arteries" dominate long-range electron transport, while BPI "capillaries" mediate short-range transport and electron transfer between the storage materials and the carbon electrode.

Synthesis of molybdenum alkylidene complexes that contain the 2,6-dimesitylphenylimido ligand.

Compounds that have the formula M(NR)(CHR')(OR″)(Pyrrolide), where OR″ is "large" relative to NR and M = Mo or W, have been shown to be Z-selective olefin metathesis catalysts. In this communication we report a new route to Mo complexes in which the relationship between NR and OR″ has been reversed; i.e., the imido ligand is the sterically demanding 2,6-dimesitylphenylimido ligand (NAr*).

Z-Selective and Syndioselective Ring-Opening Metathesis Polymerization (ROMP) Initiated by MonoAryloxidePyrrolide (MAP) Catalysts.

We report the Z-selective and syndioselective polymerization of 2,3-bis(trifluoromethyl)bicyclo[2.2.1]hepta-2,5-diene (NBDF6) and 3-methyl-3-phenylcyclopropene (MPCP) by monoaryloxide monopyrrolide imido alkylidene (MAP) catalysts of Mo. The mechanism of polymerization with syn-Mo(NAd)(CHCMe(2)Ph)(Pyr)(OHIPT) (1; Ad = 1-adamantyl, OHIPT = O-2,6-(2,4,6-i-Pr(3)C(6)H(2))(2)C(6)H(3)) as the initiator is proposed to consist of addition of monomer to the syn initiator to yield a syn first insertion product and propagation via syn insertion products. In contrast, the mechanism of polymerization with syn-Mo(NAr)(CHCMe(2)Ph)(Pyr)(OTPP) (4; Ar = 2,6-i-Pr(2)C(6)H(3), OTPP = 2,3,5,6-Ph(4)C(6)H) as the initiator at -78 °C consists of addition of monomer to the syn initiator to yield an anti first insertion product and propagation via anti insertion products. Polymerizations of NBDF6 and MPCP at room temperature initiated by 4 led to polymers without a regular structure. We propose that the syndiotacticity of cis polymers is the consequence of the required inversion at the metal center with each insertion of monomer, i.e., stereogenic metal control of the polymer structure. We also propose that the two mechanisms for forming cis,syndiotactic polymers arise as a consequence of the relative steric bulk of the imido and phenoxide ligands.

Elusive trimethyllanthanum: snapshots of extensive methyl group degradation in la--Al heterobimetallic complexes.

Reactions of [La(AlMe4)3] and [Y(AlMe4)3] with PMe3 show that the phosphine can cleave Ln--CH3--Al linkages, separating Me3Al(PMe3). PMe3 (3 mol equiv) reacts with [Y(AlMe4)3] to give [(YMe3)n] contaminated with by-products containing phosphorus and aluminum. The La-based analog, [(LaMe3)n], is not formed selectively from the reaction of [La(AlMe4)3] with PMe3 or Et2O, which rather yields insoluble La/Al heterobimetallic products. Three multi-nuclear La-based clusters were obtained from a reaction of [La(AlMe4)3] with PMe3 (1 equiv) and identified by X-ray structure analyses. Each cluster exhibits extensive methyl group degradation and contains methylene, methine, or carbide moieties. [La4Al8(CH)4(CH2)2(CH3)20(PMe3)] has a [La4(CH)4] cuboid core supported by AlMe3, Me2AlCH2AlMe2, and PMe3 ligands. [La4Al8(C)(CH)2(CH2)2(CH3)22(toluene)] also contains a cuboid core, [La3Al(C)(CH)2(CH2)], which includes one exo cubic lanthanum atom, and is supported by AlMe3, Me3AlCH2AlMe2, (AlMe4)-, and toluene ligands. The lanthanum atoms in [La5Al9(CH)6(CH3)30] are arranged in a trigonal bipyramidal fashion with (CH) functionalities capping each face. The [La5(CH)6]3- core is formally balanced by three AlMe2 + moieties and is additionally supported by six AlMe3 ligands. The unit cell contains two independent La5 clusters, one with pseudo-C3h and the other with pseudo-D3 symmetry, as well as two molecules of the separation co-product Me3Al(PMe3).