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. 2018 Nov;24(11):2041–2048. doi: 10.3201/eid2411.180451

Table 1. Rickettsia rickettsii acquisition infestation 1 with Amblyomma aureolatum ticks on 6 guinea pigs, Brazil*.

Guinea pig Fever onset, dpi (maximum temperature, °C) IFA endpoint titer at 21 dpi† Feeding chamber‡ PCR on ticks after molting, no. infected/no. tested (% infected)
Unfed nymphs Unfed adults
1 6 (40.3) 65,536 UL + IN 10/10 (100) 10/10 (100)



UL
10/10 (100)

2 8 (40.0) 65,536 UL + IN 9/9 (100) 10/10 (100)



UL
10/10 (100)

3 8 (40.5) 8,192 UL + IN 15/15 (100) 5/5 (100)



UL
15/15 (100)

4 5 (40.7) 65,536 UL 15/15 (100)



UL + IN
15/15 (100)
8/8 (100)
5 9 (40.0) 16,384 UL 15/15 (100)



UL + IN
15/15 (100)
8/8 (100)
6 7 (40.4) 16,384 UL 15/15 (100)
UL + IN 15/15 (100) 6/6 (100)

*Each guinea pig was infested on day 0 with R. rickettsii IN and on day 3 with UL. Recovered engorged larvae and nymphs were allowed to molt to nymphs and adult ticks, respectively, which were tested by real-time PCR for presence of rickettsial DNA. dpi, days postinfestation; IFA, immunofluorescence assay; IN, infected nymphs; UL, uninfected larvae.
†Blood was collected at 21 dpi and tested by IFA with R. rickettsii antigens.
‡Tick infestations were performed on 2 feeding chambers glued to the shaved back of each guinea pig, 1 chamber receiving IN and UL, the other receiving only UL (Figure).