Jp. Obrien et Dm. Sherman, FIELD METHODS FOR ESTIMATING SERUM IMMUNOGLOBULIN CONCENTRATIONS IN NEWBORN KIDS, Small ruminant research, 11(1), 1993, pp. 79-84
Serum samples were collected from 41 newborn kids between 48-96 h of a
ge after consumption of colostrum at birth. Serum immunoglobulin (Ig)
concentrations were determined using a quantitative, spectrophotometri
c zinc sulfate turbidity assay, and total serum protein was determined
using a refractometer. A qualitative sodium sulfite precipitation tes
t was also performed to evaluate Ig content using 14%,16% and 18% sodi
um sulfite solutions. Failure of passive transfer of maternal immunity
(FPT) in newborn kids was defined as a serum Ig content of less than
1200 mg/dl, and 1200 mg/dl or above as successful passive transfer (SP
T). Based on these criteria, and using a total serum protein level of
5.4 g/dl as the cutoff point, refractometry correctly identified 17 of
17 kids (100%) with FPT and 20 of 24 kids (83.3%) with SPT. Four kids
(6.7%) with adequate serum Ig levels were misidentified as FPT. Sodiu
m sulfite precipitation at 14% correctly identified 17 of 17 kids (100
%) with FPT, but only 3 of 24 (12.5%) with SPT. Twenty-one of 24 kids
(87.5%) with adequate serum Ig levels were misidentified as FPT. Sodiu
m sulfite at 16% correctly identified all 17 kids with FPT and 19 of 2
4 kids (79.2%) with SPT. Five of 24 kids (20.8%) were misidentified as
FPT. Sodium sulfite at 18% correctly identified all 17 kids with FPT
and 22 of 24 kids (91.7%) with SPT. Only two of 24 kids (8.3%) were mi
sidentified as FPT. It was concluded that the sodium sulfite precipita
tion test, with an 18% solution, was a useful method for screening you
ng goat kids for FPT or confirming SPT in the field. Total protein det
ermination of refractometry using a cutoff value of 5.4 g/dl was also
an acceptable screening method but less reliable than the sodium sulfi
te precipitation test. When using either method as a screening test, i
t is recommended that serum from individuals with a provisional diagno
sis of FPT be submitted to a laboratory for a quantitative determinati
on of Ig concentration to avoid cases of misidentification.