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. 2015 Oct 23;144(6):1129–1141. doi: 10.1017/S0950268815002368

Table 5.

Serological and quantitative polymerase chain reaction (qPCR) assay results from goat and environmental samples collected during an outbreak of Q fever in Victoria, 2013–2014

Complement fixation test titres (IgM or IgG, C. burnetii Phase II specific) qPCR assay for C. burnetii
Age, years Cycle threshold (Ct)
Titre  <2 2–4 ⩾5 Unknown Sample type No. of samples Positive <20 20–30 30–35 >35 Inconc. Negative
8 0 1 1 0 Goat vaginal swab 15 4 2 1 1 11
16 3 2 0 0 Placenta 9 6 3 1 2 3
32 0 1 0 0 Aborted kids 22 18 3* 5 6 4 4
64 0 0 0 0 Live kid 2 2
128 0 1 0 0 Air sample (500 l) 3 1 2
Negative 28 17 4 1 Goat faeces 1 1
Inconc. 3 3 0 0 Bedding 3 1 2
Apparent prevalence 9·7% 22·7% 20·0%
*

One sample, Ct = 11·94, culture obtained from this specimen.

Inconc., Inconclusive results. For qPCR, only one target present or a single target present in only one of duplicate reactions.