Je. Grimes et al., DIAGNOSTIC SEROLOGIC TESTING OF CAGE AND AVIARY BIRDS FOR CHLAMYDIOSIS AND SUGGESTED CONFIRMATORY TESTING, Journal of veterinary diagnostic investigation, 8(1), 1996, pp. 38-44
A 2 x 2 contingency table was constructed to demonstrate the relations
hips between detectable chlamydial antibody activity and clinical heal
th status of tested birds. The table revealed that 65.5% of clinically
ill birds were antibody positive by elementary body agglutination (EB
A) (greater than or equal to 10 titers) and 59.0% were antibody positi
ve by latex agglutination (LA). Thus, EBA was slightly more sensitive
than LA in detecting antibody activity. Of the clinically normal birds
, 96.7% were antibody negative (<10 titers) by EBA and 98.3% were anti
body negative by LA, Individual serum or plasma samples from a group o
f mixed types of psittacine birds and cockatiels were tested as a sepa
rate group, and relationships between EBA-detectable antibody activity
and health status were obtained from a 2 x 2 contingency table. Sixty
-six percent of birds clinically ill with signs of chlamydiosis in the
mixed-type group were antibody positive, whereas only 32.3% of clinic
ally ill cockatiels were antibody positive. Statistical analysis of th
e contingency table using a chi-square test demonstrated that the EBA
test differentiates between individual birds on the basis of health st
atus (P < 0.001). When testing paired serum or plasma samples by EBA,
LA, and direct complement fixation (DCF), the highest percentage of si
gnificant (greater than or equal to 4-fold change) titer decreases was
detected by LA, and the highest percentage of significant titer incre
ases was detected by DCF. Examples of EBA, LA, and DCF titers in paire
d and multiple serum or plasma samples are presented to show the varie
ty of responses that can occur. Results reflected variations seen in i
ndividual testing of birds with titer variability seen in the first sa
mple tested. Additional types of testing believed necessary for confir
ming or ruling out an infectious process in birds are outlined. The cu
rrent interpretations of serologic results are given.