Loss of neurovirulence is associated with reduction of cerebral capillary sequestration during acute Babesia bovis infection
© Sondgeroth et al.; licensee BioMed Central Ltd. 2013
Received: 28 May 2013
Accepted: 13 June 2013
Published: 18 June 2013
Severe neurological signs that develop during acute infection by virulent strains of Babesia bovis are associated with sequestration of infected erythrocytes in cerebral capillaries. Serial passage of virulent strains in cattle results in attenuated derivatives that do not cause neurologic disease. We evaluated whether serial passage also results in a loss of cerebral capillary sequestration by examining brain biopsies during acute disease and at necropsy.
Cerebral biopsies of spleen intact calves inoculated intravenously with a virulent or attenuated strain pair of B. bovis were evaluated for capillary sequestration at the onset of babesiosis and during severe disease. In calves infected with the virulent strain, there was a significant increase in sequestration between the first and second biopsy timepoint. The attenuated strain was still capable of sequestration, but at a reduced level, and did not change significantly between the first and second biopsy. Necropsy examination confirmed the second biopsy results and demonstrated that sequestration identified at necropsy reflects pathologic changes occurring in live animals.
Loss of neurovirulence after serial in vivo passage of the highly virulent T2Bo strain of B. bovis in splenectomized animals is associated with a significant reduction of cerebral capillary sequestration. Previous genomic analysis of this and two other strain pairs suggests that this observation could be related to genomic complexity, particularly of the ves gene family, rather than consistent gene specific differences. Additional experiments will examine whether differential gene expression of ves genes is also associated with reduced cerebral sequestration and neurovirulence in attenuated strains.
Babesia bovis is a tick-borne apicomplexan parasite that infects cattle in tropical and sub-tropical regions worldwide. Neurological signs may accompany fever and anemia during acute infection by many virulent strains . Neurovirulence is associated with infected erythrocytes cytoadhering to endothelial cells, which subsequently leads to sequestration within cerebral capillaries [2–4]. Attenuated strains of B. bovis incapable of inducing neurovirulence are derived in vivo through rapid serial passage of parental virulent strains, and are currently used as live vaccines in endemic regions . Loss of neurovirulence associated-attenuation is hypothesized to be due to loss of endothelial cell cytoadherence and sequestration. However, the absence of sequestration has not been proven experimentally, particularly in live animals during acute infection. The mechanism of cytoadherence is postulated to involve endothelial cell binding of infected erythrocytes through interaction of the large protein gene family, Variant Erythrocyte Surface Antigen (VESA)-1, with the endothelial cell surface, similar to the mechanism of sequestration and neurovirulence in falciparum malaria involving the PfEMP1 protein family [6, 7].
In this study, we tested whether the loss of neurovirulence in animals infected with the attenuated strain is due to the absence of cerebral capillary sequestration. Temporal evaluation of capillary sequestration was performed in vivo by cerebral biopsies during acute infection, and in tissues taken at necropsy.
The T2Bo virulent strain of B. bovis and an attenuated derivative strain obtained after 29 passages in splenectomized calves was utilized. The virulent parental (T2Bo_vir) and attenuated derivative strains (T2Bo_att) have been previously validated to reflect their designated phenotypes of neurovirulence and non-neurovirulence, respectively .
The study utilized spleen intact Holstein cattle >12months of age. Calves were initially obtained at 3–6 months of age from a Washington State dairy, quarantined at the Washington State University Animal Resource Unit, and given health checks at the Veterinary Teaching Hospital (College of Veterinary Medicine, Washington State University). All cattle were free of previous B. bovis infection as determined by sourcing from the United States (which is declared free of bovine babesiosis by the World Organization for Animal Health) and by confirmation through the absence of serum antibody and parasites by cELISA (VMRD, Pullman, WA) and qPCR, respectively, as previously described . All animal procedures were approved by the Animal Care and Use Committee, #ASAF 03322–002.
Two groups of spleen intact cattle (n = 2 for each group) were intravenously inoculated with blood stabilates containing 2 × 107 infected erythrocytes (iRBC) of T2Bo_vir or T2Bo_att strain. Rectal temperature, hematocrit, and parasitemia were monitored daily. One day after the onset of fever (>103°F), animals were anesthetized, placed in sternal recumbency, and a brain biopsy performed at the Veterinary Teaching Hospital (Washington State University, Pullman WA). Cerebral cortical tissue was obtained using a 14 gauge side-cutting disposable brain biopsy needle (Ad-Tech, Racine WI). Multiple 2 mm × 1 cm pieces of biopsy tissue were fixed in 10% buffered neutral formalin for subsequent microscopic evaluation. Following the first biopsy, each animal was recovered from anesthesia and clinical signs monitored. The biopsy process was repeated within 2–3 days when clinical parameters indicated severe clinical disease. All animals were euthanized after the second biopsy while under anesthesia to evaluate capillary sequestration levels after the cessation of blood flow.
Post-mortem brain and tissue samples were collected in duplicate. One sample was placed in 10% buffered neutral formalin for fixation, and the second sample was frozen in liquid nitrogen for DNA extraction and qPCR analysis.
Formalin fixed tissues were paraffin embedded, cut into 5 micron sections, placed on glass slides and stained with Giemsa (Washington Animal Disease Diagnostic Laboratory). Sequestration of B. bovis iRBC in tissue capillaries was evaluated histologically by counting a minimum of 100 erythrocytes (RBC) in longitudinal sections of capillaries. Manual counts were performed in duplicate at 63X magnification, and the average percentage of infected erythrocytes (iRBC) in capillaries was determined for each tissue using the formula: (iRBC/total RBC) × 100. All tissue sections were examined by the same individual without knowledge of which strain the animal was inoculated with.
Quantitative PCR on collected tissues
Genomic DNA was extracted from frozen tissues (brain, lung, heart, kidney, liver, spleen, and skin) stored at −80°C. Tissues were thawed, homogenized and lysed using MP Biomedicals lysing matrix A as per manufacturer’s recommendation (MP Biomedicals, Solon OH). Following the first centrifugation step, the supernatant was incubated at 56°C with proteinase K from the Qiagen Blood and Tissue DNA Extraction Kit (Qiagen, Valencia, CA), and extracted following the manufacturer’s recommendation (Qiagen, Valencia, CA). Equivalent starting amounts of tissues (0.1 g) were processed in triplicate for each animal from each group. Quantitative PCR (qPCR) was performed using a previously published protocol targeting the merozoite surface antigen-1 gene (msa- 1), with the exception of the 5′ primer (5′-GAT GCG TTT GCA CAT GCT AAG-3′). A positive control containing 10 ng of T2Bo gDNA, and negative control of naïve cow gDNA were included [9, 10].
Comparative analysis of sequestration at different biopsy time points, and tissue parasitemia, were analyzed using a 2-way ANOVA with repeated measures or 2-way ANOVA, respectively, with each followed by Bonferroni’s multiple comparison tests. A one-tailed student’s t-test was used for parasitemia comparison in blood (Graphpad Prism v. 5.0a).
Cerebral sequestration of iRBC was observed in both T2Bo_vir and T2Bo_att infected animals throughout the experiment (Figure 1B). There was no significant difference in sequestration levels between T2Bo_vir and T2Bo_att infected animals at the onset of clinical signs (biopsy 1). However, the sequestration level in the T2Bo_vir infected animals increased significantly between the first and second biopsy (mean of 10.1% and 75.6% iRBC, respectively; p < 0.0001), as well as between the first biopsy and necropsy (mean of 10.1% and 82.8% iRBC, respectively; p < 0.0001) (Figure 1C). In contrast, there was no significant elevation in sequestration level in T2Bo_att infected animals between the first and second biopsy or first biopsy and necropsy (mean of 40.42%, 23.6%, and 29.0% respectively). The capillary sequestration level between T2Bo_vir and T2Bo_att infected animals at the time of the second biopsy and necropsy were also significantly different (Figure 1C, mean of 75.6% vs 23.6% (second biopsy), and 82.8% vs 29.0% (necropsy), respectively; p < 0.05).
Parasite numbers in tissue (copies/g) of T2Bo_vir and T2Bo_att infected animals
8.92E + 05 a [3.14E + 05]
2.06E + 05 [6.80E + 04]
6.91E + 04 [6.10E + 03]
2.07E + 04 [6.27E + 03]
2.70E + 05 [6.49E + 04]
5.21E + 04 [1.44E + 04]
4.41E + 04 [1.23E + 04]
1.30E + 04 [1.47E + 03]
1.26E + 06 a [3.31E + 05]
1.09E + 05 [1.98E + 04]
6.44E + 05 [3.16E + 05]
9.15E + 04 [4.11E + 04]
0.00E + 00 [0.00E + 00]
0.00E + 00 [0.00E + 00]
While in vivo brain biopsies provide a unique analysis during acute disease, the challenges of performing these biopsies in large animals limits the total number of animals that can be examined in a study. Nonetheless, even with a small group size, our findings that the overall sequestration was lower in T2Bo_att infected animals than those infected with the parental virulent strain are statistically significant. Factors that may impact these results include variation in the initial or circulating parasite load, and differences in innate or adaptive immune response to parental and attenuated strains. Since the number of infected erythrocytes used in the inoculum for both groups was the same, the experiment was terminated prior to development of a protective immune response, and the time course of the experiment varied by only two days, the differential tissue sequestration levels observed are likely due to the nature of the inocula.
The presence of sustained sequestration with no signs of neurovirulence leads us to conclude that cytoadherence and sequestration, while associated with neurovirulence, may not be solely responsible. One explanation of the findings is that the attenuated strain may have reverted to neurovirulence once introduced back into a spleen-intact animal, a phenomenon reported experimentally in B. bovis[5, 11] and in Plasmodium spp. [12–14]. However, in the field this is uncommon as attenuated strains of B. bovis have been used for extended periods as field vaccines without reversion to virulence . The lack of neurovirulence in animals infected with T2Bo_att could be due to repertoire differences of parasite-derived proteins involved with cytoadhesion, such as the VESA1, which may then affect the binding of iRBC with endothelial cell receptors [15, 16]. Comparative genome analysis of T2Bo_vir and T2Bo_att strains reveals genomic diversity reduction, including changes in the ves gene repertoire . This finding supports the suggestion that genomic differences may contribute to phenotypic variability. Alternatively, a threshold level of iRBC cytoadherence within cerebral capillaries may be necessary for clinically expressed neurovirulence.
We hypothesized that the lack of neurovirulence in T2Bo_att infected animals is associated with an absence of cytoadherence and sequestration in cerebral capillaries. Our results demonstrate that attenuation with loss of neurovirulence does result in a significant reduction, but not total elimination of sequestration. Ongoing experiments will analyze transcriptomic expression profiles between the two members of this strain pair, and evaluate additional strain pairs in order to better understand the mechanisms of attenuation.
We thank Dr. Ignacio Echaide for providing the blood stabilates of the virulent and attenuated derivative strain pair. We also thank Ralph Horn, James Allison, Emma Karel, and Sara Davis in the USDA Animal Research Unit for animal care and technical assistance, and the Histology Section of the Washington Animal Disease Diagnostic Laboratory for preparation of tissue slides. This project is supported by National Institutes of Health Mentored Research Scientist Development grant K01-OD01154-02 and USDA cooperative agreement #58-5348-7-528.
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