Search

Recent advances in sampling techniques in the pharmaceutical industry sparked significant interest in applying improvements to extraction methods for greater analyte detection and quantitation. In particular, the dried blood spot [...]

The ability of ruminal microorganisms to degrade octahydro-1,3,5,7-tetranitro-1,3,5,7-tetrazocine (high melting explosive, HMX) as consortia from whole rumen fluid ( WRF), and individually as 23 commercially available ruminal strains, was compared under anaerobic conditions. Compound degradation was monitored by high-performance liquid chromatography, followed by liquid chromatography-tandem mass spectrometry ( LC- MS/ MS) for delineation of the metabolic pathway. In WRF, 30 μM HMX was degraded to 5 μM HMX within 24 h. Metabolites consistent with m/z 149, 193 and 229 were present throughout the incubation period. We propose that peaks with an m/z of 149 and 193 are arrived at through reduction of HMX to nitroso or hydroxylamino intermediates, then direct enzymatic ring cleavage to produce these HMX derivatives. Possible structures of m/z 229 are still being investigated and require further LC- MS/ MS analysis. None of the 23 ruminal strains tested were able to degrade HMX as a pure culture when grown in either a low carbon or low nitrogen basal medium over 120 h. We conclude that microorganisms from the rumen, while sometimes capable as individuals in the bioremediation of other explosives, excel as a community in the case of HMX breakdown. [ABSTRACT FROM AUTHOR]

• Toxicity threshold for ryegrass staggers is lowered the longer perennial ryegrass is fed. • Sub-chronic (>60 day) threshold for lolitrem B is 1554 µg/kg in Angus beef cattle. • Lolitrem B accumulates in fat tissue in a dose- and time-responsive manner. Lolitrem B is a potent tremorgen responsible for the syndrome known as "ryegrass staggers" in livestock consuming perennial ryegrass (Lolium perenne) infected with the endophyte fungus Epichloë festucae var. lolii. We evaluated clinical signs in cattle continuously fed endophyte-infected perennial ryegrass straw at four concentrations of lolitrem B (LB)/ergovaline (EV) (groups: I-2256/638, II-1554/373, III-1012/259 or IV-<300/0 µg/kg LB/EV, n =5-6 steers/group) over 64 days to establish a sub-chronic threshold of toxicity for this mycotoxin; animals were supplemented with 1 kg grain mix/day. Most animals in groups I and II developed clinical signs consistent with ryegrass staggers by day 64; thus, it is recommended that a threshold level of 1554 µg/kg LB should not be exceeded for extended feeding regimens using endophyte-infected perennial ryegrass feed material alone. This toxicity threshold is lower than that observed with shorter feeding periods, i.e. 1800–2000 µg/kg LB when fed for less than 30 days. No clinical signs associated with ergovaline toxicosis (i.e. decreased weekly weight gain) were observed. As adipose tissue appears to be the main compartment where LB is deposited, the concentration of LB and its metabolic derivatives in fat samples was determined at 37 and 64 days. Lolitrem B and three previously defined metabolites bioaccumulated in a dose- and time-dependent manner throughout the feeding experiment in fat tissue, at levels similar to those found in past research. Ratios of metabolites to LB were consistent across time points and dose groups, indicating that the enzyme(s) responsible for LB metabolism were not saturated. In summary, LB toxicity thresholds are dependent upon specificities of the dietary program including the duration feed material is fed, and should be considered when formulating safe livestock feeding regimens. [Display omitted] [ABSTRACT FROM AUTHOR]