TICK-BORNE BORRELIOSES PATHOGEN IDENTIFICATION IN IXODES TICKS (ACARINA, IXODIDAE) COLLECTED IN ST. PETERSBURG AND KALININGRAD BALTIC REGIONS OF RUSSIA
An. Alekseev et al., TICK-BORNE BORRELIOSES PATHOGEN IDENTIFICATION IN IXODES TICKS (ACARINA, IXODIDAE) COLLECTED IN ST. PETERSBURG AND KALININGRAD BALTIC REGIONS OF RUSSIA, Journal of medical entomology, 35(2), 1998, pp. 136-142
Two isolated Baltic seashore populations of Ixodes ticks were studied
as vectors of different Borrelia genospecies in Russia by using darkfi
eld microscopy and modified polymerase chain reaction (PCR). In the Ka
linigrad region (Kurish Spit. forests near the settlements of Lesnoye
and Rybachy), 788 Ixodes ricinus (L.) adults and nymphs were collected
by nagging and studied Ip darkfield microscopy during 1995-1996. Ther
e were 88 darkfield microscopy positive specimens (11.2%) of which 69
were also analyzed by PCR. Borrelia afzelii tend B. garinii were found
individually and together in ticks. In this region, on the Kurish Spi
t, 7 patients with tick; borrelioses were observed: 2 in the Russian p
art of Spit and 5 in the Lithuanian par?. A significant difference was
found between Borrelia prevalence during the spring and fall peaks of
tick abundance. Specimens that were darkfield microscopy positive pre
vailed in the fall (25.15%) in comparison with the spring peak (7.3%).
The number of specimens with identified genospecies prevailed in the
spring: 22 out of 35 versus 4 out of 31 in the fall. Among 29 PCR posi
tive I. ricinus, 21 contained B. afzelii, 3 had B. garinii, and 2 had
dual infection. In 1995, only B. afzelii infected specimens were obser
ved. In the vicinity of St. Petersburg (the seashore of;he northern Gu
lf of Finland, in forests near Lisy Nos, Morskaja) during 1992-1996, 3
1 patients with a tick-borne borrelioses were registered. We collected
487 Ixodes persulcatus Schulze by flagging and studied them by darkfi
eld microscopy in 1995-1096 of which 144 ticks (29.6%) were darkfield
microscopy positive. Sixty darkfield-positive specimens mere analyzed
by PCR, and in 88.3% of cases genospecies were identified. B. afzelii
and B. garinii were identified individually and together in ticks. In
1995, I. persulcatus with dual infection prevailed with 11 out of 21 (
52.4% positive), whereas in 1996, most I. persulcatus ticks rs contain
ed B., gn,garinii (81.2%). Dual infection was observed in 4 of 32 (12.
5%) ticks. Dual infections in I. persulcatus females increased within
the seasonal peal; of tick activity as was observed in 1995 auld in 19
96. Many patients not only had erythema migrans, but also exhibited ea
rly neurological symptoms that coincided with the number of tick vecto
rs that had dual infections in June, indicating that these patients we
re bitten by female ticks that had dual infections. A significant diff
erence existed between levels of infection in I. ricinus and I. persul
catus, with all 3 types of Borrelia infection observed 2 times more of
ten in I. persulcatus than in I. ricinus and dual infection occurred i
n I. persulcatus 3.7 times more often. It appeared that I. persulcatus
is a much more dangerous vector of tick-borne borrelioses than I. ric
inus.