USE OF SALMONELLA-TYPHIMURIUM WG49 TO ENUMERATE MALE-SPECIFIC COLIPHAGES IN AN ESTUARY AND WATERSHED SUBJECT TO NONPOINT POLLUTION

The occurrence of male-specific RNA (FRNA) coliphages, proposed as indicators of enteric viruses, was determined in an estuary subject to nonpoint pollution that included fecal inputs from livestock. A host originally developed for detecting FRNA phages in sewage was applied to water and sediment samples. Phages were enumerated using the host Salmonella typhimurium WG49 containing an Escherichia coli plasmid coding for sex pili, and the female parent strain WG45. FRNA phages and fecal coliforms were enumerated in samples collected seasonally from an estuary and associated feeder streams and densities related to selected environmental parameters. Mean phage densities enumerated on WG49 ranged from < 1 to 50 100 ml-1 water and < 13 to 7200 100 g-1 dry sediment. Examination of 300 phages from estuarine and freshwater samples showed that greater-than-or-equal-to 99% were RNase-resistant, greater-than-or-equal-to 94% were lytic to the female parent salmonella strain (WG45), less-than-or-equal-to 9% were lytic to male E. coli C3000, and none were lytic to female E. coli C. RNase resistant phages lytic to both salmonella strains were noncontractile flexible tailed phages and those lytic to male salmonella or E. coli hosts were filamentous phages. Electron micrographs of the only RNase-sensitive phage recovered that plaqued only male hosts showed cubic phage particles adsorbed to sex pili. Parallel enumerations of environmental samples on WG45 and WG49 yielded equal or greater phage densities on the former host. Purified phages from these samples were lytic to certain salmonella serovars recovered from the environment but did not cross react with fecal coliform or heterotrophic bacteria isolated from the environment. Although the WG49 host was inappropriate to estuarine and freshwater samples examined because of interference by somatic phages, WG45 and WG49 should be examined as hosts for enumerating salmonella phages. Similarly, the public health significance of somatic phages detected by these hosts should be determined. FRNA phages, with a single exception (1/187 samples), were not detected in a condemned shellfish growing area subject to nonpoint pollution. This observation questions the application of FRNA phages as indicators of fecal contamination in waters impacted by diffuse fecal inputs.