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Table 1 Experimental design of control and treatment protocols for PRRSv challenge and antimicrobial treatments

From: The impacts of viral infection and subsequent antimicrobials on the microbiome-resistome of growing pigs

Treatment groupa

PRRSv challenge

Antimicrobial exposures

Individual pigs

In-water

In-feed

UDDb

Minimal (N=36)

None/negative

As-needed to treat disease (penicillin G procaine or lincomycin HCl)

None

None

15

Moderate (N=36)

Experimentally-infected (2×10^3.5 TCID50 of a PRRSv 1-7-4 field isolate, intramuscularly)

As-needed to treat disease (penicillin G procaine or ceftiofur crystalline free acid)

Pulmotil® AC (tilmicosin phosphate, 250 mg/mL) for 5 days, starting 5 days post-PRRSv challenge

None

238

Intensive (N=36)

Experimentally infected (2×10^3.5 TCID50 of a PRRSv 1-7-4 field isolate, intramuscularly)

EXCEDE® (ceftiofur crystalline free acid, 5 mg/mL) to every pig, starting 7 days post-PRRSv challenge

Pulmotil® AC (tilmicosin phosphate, 250 mg/mL) for 5 days, starting 5 days post-PRRSv challenge

Chlortetracycline (400g/ton) and tiamulin, (35g/ton) for 14 days, starting 13 days post-PRRSv challenge

946

  1. aAll groups received modified live PRRSv vaccine (Ingelvac PRRS® MLV, Boehringer Ingelheim Vetmedica Inc., 2mL/pig) 10 days post-weaning
  2. bUsed daily doses were calculated as the total number of pig-days of treatment summed across all active ingredients; chlortetracycline and tiamulin were defined as a combined product as one of the treatments [41]