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All issues Volume 18 / No 3 (August 2011) Parasite, 18 3 (2011) 229-234 Full HTML
Open Access
Issue
Parasite
Volume 18, Number 3, August 2011
Page(s) 229 - 234
DOI https://doi.org/10.1051/parasite/2011183229
Published online 15 August 2011

© PRINCEPS Editions, Paris, 2011, transferred to Société Française de Parasitologie

Licence Creative CommonsThis is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

Introduction

Babesiosis is a parasitic infection due to the multiplication of Babesia sp. in erythrocytes (Levine, 1985; Piesman, 1987). Genus Babesia consists of group of intracellular parasites with around hundred species. Clinical signs of disease caused by Babesia, babesiosis, are variable including fever, icterus, hemoglubinuria and anemia in the host (Uilenberg, 2001; Yakhchali & Hossein 2006). These tick borne parasites infect a wide variety of vertebrate hosts including small ruminants (sheep and goat) and cattle (Persing & Conrad, 1995). In Pakistan ticks belonging to Haemophysalis sp. and Hyalomma sp. are involved in the transmission of various piroplasms to small and large ruminants (Rehman et al., 2004).

The economic losses due to babesiosis in sheep and goat production are significant in tropical and subtropical areas (Mehlhorn & Schein, 1984; Bai et al., 2002) and remain an important impediment to meat and milk production because infected animals exhibit high parasitemia and mortality (Caracappa, 1999). Babesiosis in domesticated small ruminants is due to at least three species Babesia motasi, Babesia crassa and Babesia ovis (Friedhoff, 1988). Babesia ovis is pathogenic especially in sheep and its case-fatality in susceptible hosts range from 30 to 50 % in field infections (Hashemi-Fesharki, 1997). It leads to significant losses among small ruminants due to its drastic effect on hemobiotic system (Radostits et al., 2000).

The diagnosis of small ruminant piroplasmosis is based on the microscopic examination of Giemsa stained blood smears and clinical symptoms in acute cases. After acute infections, recovered animals frequently sustain sub clinical infections, which are microscopically undetectable (Calder et al., 1996). They can be considered as a source of infection for the potential vector causing natural transmission of the disease. Serological methods are frequently employed in determining sub clinical infections. However, serology for detecting carrier state lack specificity and sensitivity, especially for infection status (Passos et al., 1998). Therefore, DNA amplification methods, which are more sensitive and specific than other conventional methods may facilitate and use a powerful tool for the diagnosis of babesiosis (Aktas et al., 2005, Altay et al., 2005, Nagore et al., 2004).

The aim of the present study was to optimize a specific, reliable and sensitive molecular tool, the polymerase chain reaction (PCR), for the detection of Babesia sp. in blood of small ruminants as parasite cannot easily be diagnosed by examination of stained blood film and negative microscopic examination does not exclude the possibility of infection. The objective of this pilot study is to provide baseline data regarding the prevalenece of Babesia sp. and risk factors involved in the spread of babesiosis in southern Punjab as to our knowledge, this parasite has never been reported in Pakistan.

Materials and Methods

Whole blood samples were collected from 107 clinically healthy small ruminants (40 sheep, 67 goats) from randomly selected herds from seven districts (Multan, Muzaffar Garh, Layyah, Dera Ghazi Khan, Khanewal, Vehari and Bahawalnagar) in the important livestock production regions of Southern Punjab (Fig. 1). Blood of 10 % animals from each herd was sampled from jugular vein in Eppendorf tubes and preserved by adding few drops of 0.5 M EDTA. Data on the characteristics of animals (species, gender, age, tick presence or absence, prior treatment for babesiosis) and the herd (location, size, species of animals, dogs associated with the herds, presence of ticks on dogs associated with the herds) was collected through questionnaires completed by the investigators on the spot during sample collection in order to calculate the risk factors involve in the spread of babesiosis. All the experiments were approved by the research and ethic committee of Bahauddin Zakariya University Multan, Pakistan.

thumbnail Fig 1.

Map of Punjab. Sampling sites in southern Punjab are marked with circles.

Inorganic method of DNA extraction was used following Shaikh et al. (2005). The quality of the DNA extract in regard to purity and integrity was assessed with optical density counts at 260/280 nm and submerged gel electrophoresis. A pair of oligonucleotide primers was used to amplify the 146 bp region of 18S rRNA gene of Babesia sp. (Nucleotide sequence data reported in this paper are available in GenBank, EMBL and DDBJ databases under accession numbers AY150058, AY534883, AY150061, AY048113) following Theodoropoulos et al. (2006).

PCR was performed in 50 μl of a mixture containing about 500 ng of template DNA, 1X PCR buffer, 10 pmol of each primer, 0.2 mM of dNTPs, 1.5 mM MgCl2, 1 % betaine solution and 1 U of Taq DNA polymerase (Vivantis, UK). Remaining volume was adjusted with double distilled water. PCR amplification was obtained after 35 cycles. Each cycle consisted of a denaturing step of 1 min at 95 C, an annealing step of 1 min at 56 C and an extension step of 1 min at 72 C. Distilled water and Babesia sp. DNA (previously isolated from naturally infected sheep, GenBank accession no. AY998123) were used in each test as negative and positive controls, respectively. Ten microliters of the amplification products were visualized on 2 % agarose gel stained with ethidium bromide and observed under UV illumination.

For statistical purposes animals were grouped into two age categories: less than 1-year and more than 1-yearold. Herds were divided into two size categories: herds composed of 1-15 and herds with more than 15 animals. Also, herds were divided according to their composition into three categories: herds with sheep only, herds with goat only and herds containing both sheep and goats. The tick burden of sheep, goats and dogs associated with the herds was also scored. Association between the presence (positive and negative blood samples) of Babesia and the various parameters, i.e. herd location, herd size, species, gender and age of animal, herd composition, presence or absence of ticks on sheep and goats, presence or absence of ticks on dogs associated with the herd was assessed by contingency table analysis using the Fisher’s exact test (for 2 × 2 tables). Statistical package Mini Tab (Version 16) was used for statistical analysis.

Results and Discussion

Results of PCR amplification revealed that 36 out of 107 sampled sheep and goats were positive for Babesia sp. 20 sheep and 16 goat blood samples were parasite positive. The parasite prevalence varied between 18 % (Dera Ghazi Khan district) to 60 % (Layyah district). Sampling sites, total number of samples collected and positive sample along with prevalence details are mentioned in Table I. Table II presents the prevalence of Babesia sp. in sheep and goats in relation to the parameters describing the characteristics of the animals while Table III shows the characteristics of herds associated with the incidence of babesiosis.

Table I.

Sampling sites along with the total number of samples collected (N) from each district. Prevalence of parasite is given in parenthesis.

Table II.

Association between parasite prevalence in goats and sheep and the studied parameters describing animal characters.

Table III.

Association between parasite prevalence in sheep and goats and the studied parameters describing animal and herd characters.

DNA amplification by PCR is a sensitive and specific tool as compared to other conventional methods (blood smear formation and serological studies) for the diagnosis of babesiosis (Aktas et al., 2005; Altay et al., 2005; Nagore et al., 2004). The small subunit (SSU) 18S rRNA gene is one of the most important markers for PCR based detection of several parasites including Babesia sp. as it is part of the ribosomal functional core and is exposed to similar selective forces in all living beings (Criado-Fornelio et al., 2003).

In the present study, among 107 sampled animals 36 (34 %) were positive for Babesia sp., which shows the high prevalence of this parasite in southern districts of Punjab. The results indicated that male sheep and goats (54 %) were more infected than females (23 %). This association between gender and parasite prevalence was statistically significant (P = 0.009) (Table II). Our results are contradictory to Theodoropoulos et al. (2006) who reported 17 % prevalence of Babesia ovis in female sheep and goats in Greece but they did not find any infected male. Our results demonstrated that animals less than one year old (61 %) were more affected with parasite as compared to older animals (Table II) and this association was statistically significant (P = 0.01) indicating that probably the animals develop immunity against parasite with age. Similar finding were reported by Razmi et al. (2003).

We also observed an association, although statistically non significant (P = 0.522), between tick burden and parasite prevalence 45 % of the sampled animals having tick present on them were positive for Babesia sp. (Table II) confirming the previous findings by Theodoropoulos et al. (2006) and. (Atlay et al. 2005) that ticks are involved in the spread of babesiosis.

Among the characters of herds, we observed that herds having more than 15 animals were more affected (P = 0.007) with the parasite (51 %) than herds composed of less than 15 animals (Table III). Also herd consisting of both sheep and goat had more Babesia sp. positive animals (P = 0.022) than herds containing sheep or goats only (Table III). Our results coincide with the findings of Theodoropoulos et al. (2006) indicating that over crowding of animals is a potential risk factor for the spread of babesiosis.

Results indicated that the presence of dog was a primary source of tick transmission (58 %) to small ruminants as the herds with dogs had higher prevalence of parasite (P = 0.003) than those without dogs (Table III). Also herds having dogs with tick burden had 55 % infected animals indicating that the vector, ticks, might have reached the small ruminants through dogs. This association between tick burdens on dog and parasite prevalence was statistically significant (P = 0.011) complementing the finding of Theodoropoulos et al. (2006).

Sheep were more susceptible for babesiosis than goats in the present study. The prevalence of Babesia sp. in sheep was 50 % as compared to 24 % infected goats (Table I). Friedhoff (1997) had reported that Babesia sp. causes diseases exclusively in sheep and rarely in goats. Moreover, males and sheep less than one year old sheep were more affected as compared to female and sheep older than one year but all these associations were statistically non significant (Table II). Our results coincide with the findings of Friedhoff (1997) that younger sheep are more prone to parasites due to developing immune system. Analysis of the data from sampled goats revealed similar findings as in sheep (Table II).

There is hardly any report on the prevalence of babesiosis in ruminants of Pakistan. To our knowledge this is the first report describing the survey on ovine babesiosis in small ruminants through PCR amplification in southern Punjab. High prevalence of Babesia sp. indicates that other species of this genus might be existing as well. In the present study, all 107 small ruminants were raised locally indicating that the babesiosis is endemic in this region. A major reason for high prevalence of parasite in southern Punjab could be the poor hygienic conditions and poverty especially in small towns and villages. In many cases, veterinarians are not available for the help and guidance of livestock owners. By generating the public awareness regarding the risk factors, the prevalence of piroplasms can be significantly decreased resulting in better health and output of sheep and goats.

Acknowledgments

This study was sponsored by Research and External Linkages Division, Bahauddin Zakariya University, Multan (Pakistan). The investigators are grateful to all the veterinarians for their help in blood sample collection.

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All Tables

Table I.

Sampling sites along with the total number of samples collected (N) from each district. Prevalence of parasite is given in parenthesis.

In the text
Table II.

Association between parasite prevalence in goats and sheep and the studied parameters describing animal characters.

In the text
Table III.

Association between parasite prevalence in sheep and goats and the studied parameters describing animal and herd characters.

In the text

All Figures

thumbnail Fig 1.

Map of Punjab. Sampling sites in southern Punjab are marked with circles.
In the text

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