TY - JOUR
T1 - Pig-associated Lawsonia intracellularis in various on-farm dipterous fly stages
AU - McOrist, Steven
AU - Blunt, Ruth
AU - Gebhart, Connie J.
PY - 2011/9/1
Y1 - 2011/9/1
N2 - Objective: To characterize the potential of pig-associated Diptera flies to carry Lawsonia intracellularis. Materials and methods: On 15 British farms, invertebrate communities were trapcollected (14 per year), counted, and sorted into species groups. Lawsonia serological tests were conducted and total DNA was extracted from pig feces; DNA was also extracted from adult flies, pupae, and larvae samples and viscera of Blatta species. Each DNA sample was tested for L intracellularis by polymerase chain reaction; positive samples were subtyped via specific variable number tandem repeat analysis. Results: The pig-associated fly community was generally dominated by Musca domestica (house fly; n = 13 farms), but on one farm each, Ophyra species (garbage fly) or Drosophila species (fruit fly) were dominant. Also noted were Muscina stabulans (false stable fly), Stomoxys calcitrans (stable fly), and Eristalis species (hover flies); Blatta orientalis cockroaches were noted on two farms. Lawsonia infections were routinely detected in nursery pigs on 14 farms. On five of 12 Lawsonia-posmve farms with Musca-dom'mant insects, Lawsonia DNA was detected widiin numerous flies (22% to 75% of fly samples from nursery pens). On two farms, larval forms of Eristalis from pen floors were also Lawsonia-posmve. Subtyping indicated that the same Lawsonia isolate occurred within pigs and the pig-associated fly stages (Musca adults and Eristalis larvae). The DNA extracted from cockroach samples, and from other flies, was negative. Implication: Musca and Eristalis flies have the greatest potential to carry and transmit Lawsonia intracellularis due to their pigassociated life cycle stages.
AB - Objective: To characterize the potential of pig-associated Diptera flies to carry Lawsonia intracellularis. Materials and methods: On 15 British farms, invertebrate communities were trapcollected (14 per year), counted, and sorted into species groups. Lawsonia serological tests were conducted and total DNA was extracted from pig feces; DNA was also extracted from adult flies, pupae, and larvae samples and viscera of Blatta species. Each DNA sample was tested for L intracellularis by polymerase chain reaction; positive samples were subtyped via specific variable number tandem repeat analysis. Results: The pig-associated fly community was generally dominated by Musca domestica (house fly; n = 13 farms), but on one farm each, Ophyra species (garbage fly) or Drosophila species (fruit fly) were dominant. Also noted were Muscina stabulans (false stable fly), Stomoxys calcitrans (stable fly), and Eristalis species (hover flies); Blatta orientalis cockroaches were noted on two farms. Lawsonia infections were routinely detected in nursery pigs on 14 farms. On five of 12 Lawsonia-posmve farms with Musca-dom'mant insects, Lawsonia DNA was detected widiin numerous flies (22% to 75% of fly samples from nursery pens). On two farms, larval forms of Eristalis from pen floors were also Lawsonia-posmve. Subtyping indicated that the same Lawsonia isolate occurred within pigs and the pig-associated fly stages (Musca adults and Eristalis larvae). The DNA extracted from cockroach samples, and from other flies, was negative. Implication: Musca and Eristalis flies have the greatest potential to carry and transmit Lawsonia intracellularis due to their pigassociated life cycle stages.
KW - Eristalis
KW - Lawsonia intracellularis
KW - Musca
KW - Proliferative enteropathy
KW - Swine
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M3 - Review article
AN - SCOPUS:80052686764
SN - 1537-209X
VL - 19
SP - 277
EP - 283
JO - Journal of Swine Health and Production
JF - Journal of Swine Health and Production
IS - 5
ER -