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K B Logan

Publications and source records attributed to K B Logan.

4 recordsLinked to original sources

Methods for studying aquatic bacteriophage ecology.

Methods are described for enumerating the different kinds of bacteriophage present in virus concentrates prepared from 120 liters of water. Although developed specifically for use with coliphages, they should be applicable to viruses infecting other hosts. These methods involve mixed indicators, equilibrium buoyant-density centrifugation, use of enzymes or inhibitors or both, and specific hybridization probes, either alone or in combination. With these methods, it was possible to specifically enumerate filamentous and isometric male-specific (F-specific) phages, the different classes of P-group plasmid-specific phages, phiX174-like phages, and lambda-like phages. Some applications of these methods, including measurement of virus inactivation in the environment and the extent of fecal pollution, are discussed.

Journal Article↗

A portable device for the rapid concentration of viruses from large volumes of natural freshwater.

A portable device for the rapid concentration of viruses from natural freshwaters described and its performance in field use is evaluated. The system handled up to 500 litres of water in less than 90 min at a cost of only 2 pounds per sample. Where the samples contained sufficient bacteriophages for detection by direct plating the apparent phage recoveries were greater than 75%. Plant and animal viruses were also concentrated from waters with this system.

Bacteriophages↗

Rapid concentration of bacteriophages from large volumes of freshwater: evaluation of positively charged, microporous filters.

Microporous, positively charged Zeta Plus 60 S filters were evaluated for bacteriophage recovery from large volumes of natural water. A variety of phages adsorbed efficiently to the filter medium at water pH levels below neutrality, but adsorption was reduced above pH 7. Adsorbed phages were easily eluted with an arginine/1% beef extract solution, pH 9.0. A concentration procedure suitable for the field isolation of bacteriophages from large volumes of river water was devised. The procedure involves, (1) prefiltration through 10" cartridge depth filters, (2) adjustment of water pH to pH 5.5--6.0, (3) adsorption of the phages on to Zeta Plus 60 S filters, (4) elution of bound phage in a small volume of eluent, (5) secondary concentration by ultrafiltration of the resulting eluates. Using this procedure, bacteriophages in 65 1 of river water was concentrated to 35 ml with recoveries in the range 50--60%.

Adsorption↗

Generation of defective interfering particles of Semliki Forest virus in a clone of Aedes albopictus (mosquito) cells.

Serial undiluted passage of Semliki Forest virus in a clone of Aedes albopictus cells resulted in a marked decrease in infectious virus yields due to the generation and accumulation of defective interfering particles. Virus from the third passage had a high particle/infectivity ratio and interfered specifically with homologous but not heterologous standard virus replication. Two RNA species of molecular weights 0.78 X 10(6) and 0.61 X 10(6) were the major RNA components of purified passage 4 virus. These RNA species were also the predominant virus RNA species detected in cells infected with passage 3 virus. Synthesis of standard virus RNA and virus-specified protein was much reduced in passage 3 virus-infected cells. Interference with standard virus replication and the synthesis of large amounts of defective interfering RNA were also observed in chicken embryo cells infected with passage 3 virus from mosquito cells.

Aedes↗