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. 2005 Aug;187(16):5776–5781. doi: 10.1128/JB.187.16.5776-5781.2005

TABLE 4.

Artificial feeding of larvae and nymphs with three strains of spirochetesa

Strain No. positive for infection/total no. (%)
Immersed larvaeb
Capillary-fed nymphsc
1-day hold
3-day hold
1 wk 3 wk 1 wk 3 wk 1 wk
B31-A3 12/15 (80) 9/15 (60) 23/23 (100) 21/22 (95.5) 23/28 (82.1)
A3-pB 3/11 (27.3)* 1/10 (10)* 3/26 (11.5)* 2/25 (8)* 0/21 (0)*
A3-pB22 10/14 (71.4) 4/13 (30.8) 13/24 (54.2)* 14/21 (67.7)* 2/34 (5.9)*
a

*, infection rate was significantly different than the infection rate of ticks that fed on B31-A3-injected mice for each column (P < 0.05, Fisher's exact test).

b

Immersed larvae were tested for infection at 1 and 3 wk after placement on mice. Of the mice fed on by B31-A3-infected, A3-pB-infected, or A3-pB22-infected larvae, respectively, one of one, zero of one, and one of one tested positive for infection.

c

Nymphs were held for 1 or 3 days after capillary feeding before placement on mice and then tested for infection 1 and 3 wk after placement on mice. Of the mice fed on by B31-A3-infected, A3-pB-infected, or A3-pB22-infected nymphs held for 1 day, two of two, zero of two, and one of two mice, respectively, tested positive for infection.