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Experimental infections of rabbits with proliferative and latent stages of Besnoitia besnoiti.

Liénard E, Pop L, Prevot F, Grisez C, Mallet V, Raymond-Letron I, Bouhsira É, Franc M, Jacquiet P - Parasitol. Res. (2015)

Bottom Line: Clinical follow-up and blood sampling for serological survey and qPCR were performed during 10 weeks until euthanasia.Seroconversion occurred in group T without any clinical signs.The proposed model could be used to assess the in vivo effectiveness of vaccine or drugs against cattle besnoitiosis.

View Article: PubMed Central - PubMed

Affiliation: UMR INRA/DGER 1225, INP - École Nationale Vétérinaire de Toulouse, Laboratoire de Parasitologie, 23 chemin des Capelles, F-31076, Toulouse, France, e.lienard@envt.fr.

ABSTRACT
Cattle besnoitiosis due to Besnoitia besnoiti is spreading across Europe and is responsible for severe economic losses in newly infected herds. Experimentally speaking, rabbits have been found to be susceptible to this parasite. The adaptation of B. besnoiti to rabbits may offer a new, easier and cheaper model of investigation for this disease. This study compared the virulence between tachyzoites and bradyzoites of B. besnoiti in rabbits. Eighteen New Zealand rabbits were allocated into three groups of six animals each. The rabbits from the control (group C), "tachyzoite" (group T) and "bradyzoite" (group B) groups were subcutaneously injected in the right flank with 66 μg of ovalbumin, 6.10(6) tachyzoites (125th passage on Vero cells) and 6.10(6) bradyzoites (collected from a natural infected cow) of B. besnoiti, respectively. Clinical follow-up and blood sampling for serological survey and qPCR were performed during 10 weeks until euthanasia. Molecular and immunohistochemistry examination was achieved on 25 samples of tissue per rabbit. Seroconversion occurred in group T without any clinical signs. Rabbits of group B exhibited a febrile condition (temperature above 40 °C from day 8 to day 11 following injection) with positive qPCR in blood. Cysts of B. besnoiti were found on skin samples and organs of rabbits from group B in tissue explored with threshold cycle (Ct) values below 30. These results suggest a higher virulence of bradyzoites in rabbits than Vero cell-cultivated tachyzoites. The proposed model could be used to assess the in vivo effectiveness of vaccine or drugs against cattle besnoitiosis.

No MeSH data available.


Related in: MedlinePlus

Kinetics of the mean humoral immune response (± standard deviation bars) from each rabbit group. Rabbits were experimentally subcutaneously challenged with 66 μg of ovalbumin (group control), 6.106 tachyzoites (group tachyzoites) and 6.106 bradyzoites (group bradyzoites) of B. besnoiti at day 0. The dashed lines indicate the cut-off value for IgG-IFAT (200). Two dates (day 9 and day 17) were missing for control and tachyzoite groups
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Fig3: Kinetics of the mean humoral immune response (± standard deviation bars) from each rabbit group. Rabbits were experimentally subcutaneously challenged with 66 μg of ovalbumin (group control), 6.106 tachyzoites (group tachyzoites) and 6.106 bradyzoites (group bradyzoites) of B. besnoiti at day 0. The dashed lines indicate the cut-off value for IgG-IFAT (200). Two dates (day 9 and day 17) were missing for control and tachyzoite groups

Mentions: No positive seroconversion occurred in group C as determined by WB (Table 1, Fig. 2a) and by IFAT (titre <100, Fig. 3).Table 1


Experimental infections of rabbits with proliferative and latent stages of Besnoitia besnoiti.

Liénard E, Pop L, Prevot F, Grisez C, Mallet V, Raymond-Letron I, Bouhsira É, Franc M, Jacquiet P - Parasitol. Res. (2015)

Kinetics of the mean humoral immune response (± standard deviation bars) from each rabbit group. Rabbits were experimentally subcutaneously challenged with 66 μg of ovalbumin (group control), 6.106 tachyzoites (group tachyzoites) and 6.106 bradyzoites (group bradyzoites) of B. besnoiti at day 0. The dashed lines indicate the cut-off value for IgG-IFAT (200). Two dates (day 9 and day 17) were missing for control and tachyzoite groups
© Copyright Policy - OpenAccess
Related In: Results  -  Collection

Show All Figures
getmorefigures.php?uid=PMC4562009&req=5

Fig3: Kinetics of the mean humoral immune response (± standard deviation bars) from each rabbit group. Rabbits were experimentally subcutaneously challenged with 66 μg of ovalbumin (group control), 6.106 tachyzoites (group tachyzoites) and 6.106 bradyzoites (group bradyzoites) of B. besnoiti at day 0. The dashed lines indicate the cut-off value for IgG-IFAT (200). Two dates (day 9 and day 17) were missing for control and tachyzoite groups
Mentions: No positive seroconversion occurred in group C as determined by WB (Table 1, Fig. 2a) and by IFAT (titre <100, Fig. 3).Table 1

Bottom Line: Clinical follow-up and blood sampling for serological survey and qPCR were performed during 10 weeks until euthanasia.Seroconversion occurred in group T without any clinical signs.The proposed model could be used to assess the in vivo effectiveness of vaccine or drugs against cattle besnoitiosis.

View Article: PubMed Central - PubMed

Affiliation: UMR INRA/DGER 1225, INP - École Nationale Vétérinaire de Toulouse, Laboratoire de Parasitologie, 23 chemin des Capelles, F-31076, Toulouse, France, e.lienard@envt.fr.

ABSTRACT
Cattle besnoitiosis due to Besnoitia besnoiti is spreading across Europe and is responsible for severe economic losses in newly infected herds. Experimentally speaking, rabbits have been found to be susceptible to this parasite. The adaptation of B. besnoiti to rabbits may offer a new, easier and cheaper model of investigation for this disease. This study compared the virulence between tachyzoites and bradyzoites of B. besnoiti in rabbits. Eighteen New Zealand rabbits were allocated into three groups of six animals each. The rabbits from the control (group C), "tachyzoite" (group T) and "bradyzoite" (group B) groups were subcutaneously injected in the right flank with 66 μg of ovalbumin, 6.10(6) tachyzoites (125th passage on Vero cells) and 6.10(6) bradyzoites (collected from a natural infected cow) of B. besnoiti, respectively. Clinical follow-up and blood sampling for serological survey and qPCR were performed during 10 weeks until euthanasia. Molecular and immunohistochemistry examination was achieved on 25 samples of tissue per rabbit. Seroconversion occurred in group T without any clinical signs. Rabbits of group B exhibited a febrile condition (temperature above 40 °C from day 8 to day 11 following injection) with positive qPCR in blood. Cysts of B. besnoiti were found on skin samples and organs of rabbits from group B in tissue explored with threshold cycle (Ct) values below 30. These results suggest a higher virulence of bradyzoites in rabbits than Vero cell-cultivated tachyzoites. The proposed model could be used to assess the in vivo effectiveness of vaccine or drugs against cattle besnoitiosis.

No MeSH data available.


Related in: MedlinePlus