dAlthough many studies have reported the indirect immunofluorescence assay (IFA) to be more sensitive in detection of antibodies to Coxiella burnetii than the complement fixation test (CFT), the diagnostic sensitivity (DSe) and diagnostic specificity (DSp) of the assay have not been previously established for use in ruminants. This study aimed to validate the IFA by describing the optimization, selection of cutoff titers, repeatability, and reliability as well as the DSe and DSp of the assay. Bayesian latent class analysis was used to estimate diagnostic specifications in comparison with the CFT and the enzyme-linked immunosorbent assay (ELISA). The optimal cutoff dilution for screening for IgG and IgM antibodies in goat serum using the IFA was estimated to be 1:160. The IFA had good repeatability (>96.9% for IgG, >78.
Coxiella burnetii causes Q fever in humans as well as abortions, stillbirths, and infertility in ruminants (1-5). The organism replicates in the placenta of infected ruminants, reaching a level of up to 10 9 bacteria per gram of placenta tissue (4-6). C. burnetii organisms are shed in an extremely high concentration in birth fluids, placental tissues, and membranes of aborted fetuses as well as in milk, urine, and feces of infected ruminant animals around the parturition period (4, 5). The high concentration of C. burnetii organisms shed in tissues, fluids, and excreta of infected ruminants is the primary source of human infections (7).Caprine and ovine infections have been reported to result in severe placentitis and consequently in shedding of higher numbers of C. burnetii organisms than infections of cattle (8). Studies have also revealed that goats and sheep shed higher quantities of C. burnetii in feces, vaginal mucus, and birth tissues than other livestock (9). Thus, the risk of human transmission is higher when infections occur in herds of small ruminants than when they occur with other livestock. Unsurprisingly, the majority of reported large outbreaks of Q fever have been associated with infected sheep and goat flocks, including a major outbreak of more than 4,000 human Q fever cases in the Netherlands that was linked to sheep and goat farms with over 50 animals (9)(10)(11)(12)(13)(14). Infection with C. burnetii can be asymptomatic in many animals and may be detected in ruminants only when infection causes abortions and reproductive abnormalities in pregnant animals (1). Delay in diagnosis in livestock slows the implementation of appropriate control strategies, thus increasing the risk of human infection.Coxiellosis in animals can be diagnosed through microscopic examination of stained tissues, culture, detection of C. burnetii DNA using PCR, and detection of antibodies to C. burnetii in blood and milk (15,16). The microscopic diagnosis of coxiellosis is mainly undertaken on placental tissues using Stamp-Macchiavello coloration or Giemsa stain. The organism can be cultured in cells, embryonated hen eggs, or cell-free media (15,17). However, microscopy and culture are expensive and requi...