Efficacy of a subcutaneously administered, ultraviolet light-killed Pasteurella multocida A:3-containing bacterin against transthoracic challenge exposure in goats

Charles W. Purdy From the USDA, Agricultural Research Service, Conservation and Production Research Laboratory, PO Drawer 10, Bushland, TX 79012 (Purdy); the Department of Microbiology and Immunology, Health Science Center, Texas Tech University, Lubbock, TX 79430 (Straus), and the Texas Veterinary Medical Diagnostic Laboratory, Texas A&M University, Amarillo, TX 79106 (Ayers).

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David C. Straus From the USDA, Agricultural Research Service, Conservation and Production Research Laboratory, PO Drawer 10, Bushland, TX 79012 (Purdy); the Department of Microbiology and Immunology, Health Science Center, Texas Tech University, Lubbock, TX 79430 (Straus), and the Texas Veterinary Medical Diagnostic Laboratory, Texas A&M University, Amarillo, TX 79106 (Ayers).

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J. R. Ayers From the USDA, Agricultural Research Service, Conservation and Production Research Laboratory, PO Drawer 10, Bushland, TX 79012 (Purdy); the Department of Microbiology and Immunology, Health Science Center, Texas Tech University, Lubbock, TX 79430 (Straus), and the Texas Veterinary Medical Diagnostic Laboratory, Texas A&M University, Amarillo, TX 79106 (Ayers).

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Abstract

Objective

To determine the effectiveness of Pasteurella multocida biovar A, serovar 3 (Pm A:3) killed by exposure to UV light and incorporated with a polyacrylate bead carrier as a vaccine.

Animals

18 weanling male Spanish goats.

Procedure

Prospective, randomized controlled study with 3 treatment groups: positive-control (PC), negative-control (NC), and principal Pm A:3 bacterin (PA) groups. Six PC goats each received live Pm A:3 and polyacrylate beads twice, 22 days apart, by transthoracic injection into the left lung. Six NC goats each received only PA beads twice, 22 days apart, by transthoracic injection. Six principal goats each received Pm A:3 vaccine SC twice, 22 days apart. Fourteen days after the second vaccination, all goats were challenge exposed with live Pm A:3 by transthoracic injection into the right lung, and 4 days later they were euthanatized and necropsied.

Results

Mean volume of consolidated lung tissue at the challenge site was 1.75 cm3 for the PC group, 15.18 cm3 for the NC group, and 3.9 cm3 for the PA vaccine group. The NC group had a significantly (P ≤ 0.002) larger mean volume of consolidated lung tissue than did the PC and PA groups after challenge exposure.

Conclusions

The PA bacterin and the PC groups developed protective immunity against live Pm A:3 challenge exposure. An SC administered, UV light-killed, Pm A:3 bacterin induced protective immunity similar to that induced by virulent live Pm A:3 injected into the target organ, the lung. (Am J Vet Res 1997;58:841–847)

Abstract

Objective

To determine the effectiveness of Pasteurella multocida biovar A, serovar 3 (Pm A:3) killed by exposure to UV light and incorporated with a polyacrylate bead carrier as a vaccine.

Animals

18 weanling male Spanish goats.

Procedure

Prospective, randomized controlled study with 3 treatment groups: positive-control (PC), negative-control (NC), and principal Pm A:3 bacterin (PA) groups. Six PC goats each received live Pm A:3 and polyacrylate beads twice, 22 days apart, by transthoracic injection into the left lung. Six NC goats each received only PA beads twice, 22 days apart, by transthoracic injection. Six principal goats each received Pm A:3 vaccine SC twice, 22 days apart. Fourteen days after the second vaccination, all goats were challenge exposed with live Pm A:3 by transthoracic injection into the right lung, and 4 days later they were euthanatized and necropsied.

Results

Mean volume of consolidated lung tissue at the challenge site was 1.75 cm3 for the PC group, 15.18 cm3 for the NC group, and 3.9 cm3 for the PA vaccine group. The NC group had a significantly (P ≤ 0.002) larger mean volume of consolidated lung tissue than did the PC and PA groups after challenge exposure.

Conclusions

The PA bacterin and the PC groups developed protective immunity against live Pm A:3 challenge exposure. An SC administered, UV light-killed, Pm A:3 bacterin induced protective immunity similar to that induced by virulent live Pm A:3 injected into the target organ, the lung. (Am J Vet Res 1997;58:841–847)

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