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Emerging Infectious Diseases

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Article Contents

The Study
Conclusions
Acknowledgments
References
Table 1
Table 2
Suggested Citation

Volume 13, Number 8–August 2007

Dispatch

Babesia sp. EU1 from Roe Deer and Transmission within Ixodes ricinus

Sarah Bonnet,* Maggy Jouglin,* Monique L'Hostis,† and Alain Chauvin†
*Institut National de la Recherche Agronomique, Nantes, France; and †Ecole Nationale Vétérinaire de Nantes, Nantes, France

The Study

In January 2005 and January 2006, 89 roe deer at the Wild Fauna Reserve of Chizé (Deux Sèvres, France) were captured; blood was obtained through the jugular vein and analyzed for infection by Babesia spp. Parasites were isolated from autologous roe deer erythrocytes as described (9), except that 20% fetal calf serum (FCS) was used. Cultures were monitored for parasitemia by examination of Giemsa-stained thin blood smears. Parasites were then adapted to culture in blood from deer (Dama dama) from the Jardin des Plantes of Nantes (Loire Atlantique, France) and from sheep reared in our laboratory. Adaptation was conducted as described (10), except that 20% FCS was also used.

A total of 150 μL parasite genomic DNA was then prepared from 10-mL cultures (10% parasitemia, 2.5% hematocrit) according to the protocol of a commercial extraction kit (Promega, Madison, WI, USA) on merozoite preparations obtained by Percoll gradient centrifugation (Amersham, Uppsala, Sweden) with a density of 1.08 g/mL in 0.15 M NaCl. PCR amplifications were performed with 10 μL DNA and BAB primers (Table 1) as described (11). For positive samples, 5 μL DNA was subjected to a second amplification with EU1 primers (Table 1) as described by Hilpertshauser et al. (8), except that the annealing temperature was 63°C and uracil DNA glycosylase was not used.

During January 2005, 31 of 79 roe deer analyzed were infected with Babesia spp., as shown by parasite culture and PCR amplification with BAB primers. Of 29 cultures tested for EU1 with the corresponding primers, 59% were positive, which indicated an estimated global EU1 prevalence of 23% (Table 2). In January 2006, 5 of 10 cultures tested contained Babesia spp. parasites. Sequencing of the complete 18S rRNA gene from subcultures in autologous deer and sheep erythrocytes amplified with the primer set CRYPTO (Table 1) (4) showed that 2 of these cultures (C210 and C201) had 100% identity with the EU1 human strain (GenBank accession no. AY046575) (4). The unique sequence obtained has been deposited in GenBank (accession no. EF185818).

In January 2005, a total of 106 engorged female adult I. ricinus were collected from the 31 roe deer harboring Babesia spp. Ticks were then reared in the laboratory at 22°C and a relative humidity of 80%–90%. Forty-two ticks (from 22 roe deer) laid eggs from which larvae were analyzed for parasites with BAB primers as described (11); 64% of larvae samples had a positive reaction. Amplification products from egg sample E177.3 and larva sample L177.3 that were sequenced showed 100% identity with the 18S rRNA gene of EU1 (4). The sequence has been submitted to GenBank (accession no. EF185819). Among positive samples, 6 of 15 analyzed for EU1 with specific primers showed a positive reaction (Table 2).

Conclusions

Isolation of EU1 from roe deer in France confirms that these animals are reservoir hosts of the parasite and that EU1 is not restricted to 1 geographic area in Europe. A survey conducted in Slovenia showed that 21.6% of 51 roe deer tested were infected with EU1 (5) and a similar prevalence (23%) was observed.

To our knowledge, this is the first isolation of EU1 in culture in homologous erythrocytes and erythrocytes from other ruminants. Until now, Babesia sp. EU1 has only been detected in roe deer (5) and humans (4). It has also been detected in I. ricinus collected from sheep and goats in Switzerland (8); however, the ticks in that study may have acquired the infection at a preceding stage during a blood meal taken on another host.

In a study in Slovenia in 1997, 2.2% of 135 I. ricinus collected by flagging vegetation were positive by PCR for EU1 (6,12). PCR studies in Switzerland that examined ticks collected from domestic and wild ruminants with unknown parasitologic status showed that 1%–2% contained EU1 DNA (7,8). In our study, 40% of larvae samples from female ticks collected on Babesia-infected roe deer were infected with EU1. We assume that ticks do not necessarily become infected or transmit the parasite to the next generation after a blood meal on a EU1-infected host because 5 larval pools that originated from female ticks collected on EU1-infected roe deer were not infected (Table 2).

DNA sequences of the 18S rRNA gene were identical in parasites isolated from roe deer (C201 and C210) or I. ricinus samples. This finding indicates that deer and ticks were infected with the same organism, which may be transmitted by the tick. In addition to I. ricinus, EU1 DNA has been isolated from Haemaphysalis punctata ticks in Switzerland (8). However, during this survey, entire ticks or the apical part of fully engorged females were tested. Positive results from such samples indicated infection status only, not proof of the vectorial capacity of the tick (11).

We report that EU1 is transmitted within I. ricinus and that transovarial transmission occurs in this tick, as shown by detection of parasite DNA in eggs and larvae from females collected on roe deer. Some EU1-positive eggs and larvae can originate from adults engorged on EU1-uninfected roe deer, as observed in 3 roe deer (L128.3, L177.3, and L179.1). This finding suggests that the parasite was acquired during a preceding blood meal and that transstadial transmission occurred, at least from nymph to adult. Further investigations are needed to clarify the ability of I. ricinus to acquire and transmit Babesia sp. EU1. This species, which has been isolated from 2 human cases of babesiosis, should be studied to determine other potential reservoir hosts because of its potential as an emerging zoonotic pathogen.

Acknowledgments

We thank Norman Pieniazek for permission to use primers BAB GF2 and BAB GR2, Guy van Laere and his group for technical assistance in collecting roe deer samples, Bernard Bouet and Emmanuel Risi for efficient help in collecting fallow deer blood, Nadine Brisseau for technical assistance, and Richard Paul and Albert Agoulon for their critical reading of the manuscript.

This study was supported by research funds from the Institut National de la Recherche Agronomique and the Ecole Nationale Vétérinaire de Nantes.

Dr Bonnet is a medical entomologist and a parasitologist in the Department of Santé Animale, Institut National de la Recherche Agronomique, Nantes, France. Her research interests include analysis of pathogen transmission by ticks (including Babesia spp. and some bacteria species).

References

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Duh D, Petrovec M, Bidovec A, Avsic-Zupanc T. Cervids as Babesiae hosts, Slovenia. Emerg Infect Dis. 2005;11:1121–3.
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Tables

Table 1. Nucleotide sequences of PCR primers used for amplification and sequencing of 18S rRNA genes of Babesia spp.
Table 2. PCR detection of Babesia sp. EU1 in blood samples from roe deer and in Ixodes ricinus larvae hatched from engorged females collected from roe deer