01925     2200229   4500001002100000005001500021035002000036007000300056008003900059082001500098084001500113100001700128245008600145250001700231260007400248300000600322650001800328700001500346700001600361520130300377990001501680INLIS00000000001895220250108112510  a0010-0924000031ta250108                |          | |    aARTVET0443  aARTVET04430 aLILY NATALIA1 aPENCEGAHANENTEROTOKSEMIAPADASAPIYANG DITRANSPORTASIKAN ANTARPULAU /cLILY NATALIA  aVol. 2 No. 1  aBalai Penelitian Veteriner :bJurnal Ilmu Ternak dan Veteriner,c1996  a6 4aNTEROTOKSEMIA0 aSUDARISMAN0 aM. DARODJAT  aNATALIA. L., SUDARISMAN, and M. DARODJAT. 1996. Prevention ofenterotoxacmiu in transportedcattle. Jurnal ilmu Ternak dam Veteriner 2( I) .
Fatal enterotoxaemia oftransported cattle is frequently reported in Indonesiu. Acute enteritis andfatal enterotoxaemia of cattle andbuffaloes
in Indonesiaareassociated with toxigenic Clostridiumperfringenrtype A. Theoutbreakscouldhave been caused by somekinds of stress, such as
a possible change in nutrition or management as well as transportation. To reduce mortality rate caused by enterotoxaemia, an effective vaccine
against thedisease wasproduced. The vaccinewas made in an alum precipitated toxoid form,prepared from Clostridlumperfringenstype Atoxin,
which was then tested for safety in mice and for its capacity in generating high immunity in cattle. The vaccine was then used to immunise
transported cattle as an attemptto reduce mortality rate and to observe antibody response of cattle following vaocletdon. The results showed that
mortality in vaccinated was lower than in non-vaccinated groups of cattle. From field observation, it was obvious that alum precipitated toxoid
vaccine could produce good immune response against enterotoxaemia in cattle. It was also evidence that this vaccine could reduce mortality in
transported cattle.  aARTVET0443