Buccal micronucleus assay in human populations from Sicily (Italy) exposed to petrochemical industry pollutants.

Petroleum refinery workers are potentially exposed to a wide range of petrochemical industry pollutants (PIP), such as benzene and 1,3-butadiene, cancer-related compounds classified as carcinogenic to humans. The aim of this study was to evaluate the cytogenetic effects of exposure to PIP from two industrialised areas in South/East Sicily (Italy) using a micronucleus (MN) assay and other nuclear anomalies (ONA) on exfoliated buccal cells. Results highlighted not only a statistically significant high level of increase of MN in petroleum refinery (PR) workers, but also in the subjects not working in PR but living in the industrialised area. The ONA analysis showed a highly significant increase in karyolytic cells in exposed vs unexposed subjects, in contrast to a decrease in differentiated cells. These results suggest the presence of a cytotoxic effect in the oral mucosa cells, probably related to the pollutant compounds present in the environment close to the petrochemical industries. Our data confirm that the analysis of exfoliated buccal cells is a useful and simple non-invasive method to evaluate the genotoxic/cytotoxic effects of pollutants in a specific area. To avoid confounding factors due to the different lifestyles of the human subjects, the above assays could be better applied on farm animals, which have a relatively consistent lifestyle and, in some cases, a very low genetic heterogeneity.

Rapid molecular identification of necrophagous diptera by means of variable-length intron sequences in the wingless gene.

The arrival of arthropods at a corpse exhibits specific temporal patterns, and Diptera play a key role in the initial stages of the decomposition process. Thus, the correct species assignment of the insect larvae found on a decomposing body is an important step in forensic investigations. Here, we describe a molecular procedure to define the species at larval age found on a corpse more quickly and easily than current systems. Our method involves a unique PCR amplification of a DNA segment within the evolutionarily conserved wingless gene, involved in embryo development. The amplified DNA segment contains the fourth intron of wingless, which we found to be variable in length, from about 800 to 3000 bp, among species of necrophagous Diptera. The identification of the amplified segment size in species from Lucilia, Calliphora and Sarcophaga genera, allowed us to determine the species at larval age collected in the early stages of a decomposing body, with a simple PCR amplification and subsequent electrophoresis. This procedure may help in forensic investigations to estimate the minimum Post Mortem Interval (PMI-min) of a body colonized by these larvae, avoiding the use of time-consuming and/or more expensive procedures.