Comparative study of heavy metal and pathogenic bacterial contamination in sludge and manure in biogas and non-biogas swine farms

The objective of this study is to determine and compare the heavy metal (Zn, Cu, Cd, Pb) and bacterial (E. coli, coliform and Salmonella spp.) contamination between swine farms utilizing biogas and non-biogas systems in the central part of Thailand. Results showed that average levels of E. coli, coliform, BOD, COD, Zn, Cu and Pb in sludge from the post-biogas pond were higher than the standard limits. Moreover, the levels of E. coli, coliform, Cd and Pb were also higher than the standard limits for dry manure. The levels of E. coli, coliform and BOD on biogas farms were lower than on non-biogas farms. Following isolation of Salmonella spp:; it was found that Salmonella serovars Rissen was the most abundant at 18.46% (12/65), followed by Anatum 12.31% (8/65), and Kedougou 9.23% (6/65). The pathogenic strains of Salmonella serovars Paratyphi B var. java and Typhimurium were present in equal amounts at 4.62% (3/65) in samples from all swine farms. This study revealed that significant reduction in E. coli and coliform levels in sludge from covered lagoon biogas systems on swine farms. The presence of Salmonella as well as Cd and Pb, in significant amount in dry manure, suggests that there is a high probability of environmental contamination if it is used for agricultural purposes. Thus, careful waste and manure disposal from swine farms and the regular monitoring of wastewater is strongly recommended to ensure the safety of humans, other animals and the environment.     

Organ differences in microsomes and cytosol metabolism of Aflatoxin B1 in piglets

In order to delineate the features of aflatoxin B1 (AFB1) metabolism in various organs of piglets, in vitro metabolism of AFB1 by microsomes and cytosol of the various piglet organs was studied. The AFB1 was converted efficiently to AFP1 by the kidney microsomes. A less efficient metabolism was noted from the AFB1 to AFQ1, AFM1, and aflatoxicol (AFL) in the various organs. The microsomal ability to form AFB1-DNA adduct was higher in liver when compared to the other organs. The cytosolic glutathione-S-transferase activity to convert AFB1-epoxide to AFB1-glutathione conjugate product was relatively higher in the liver and the small intestine. The reductase activity to convert AFB1-dialdehyde to AFB1-dialcohol was similar in all the organs. The results suggest that the variation in susceptibility to the aflatoxin among different organs is attributable mainly to the organ differences in cytochrome P450 activity to form AFB1-epoxide.