Control of cystic echinococcosis in the Middle Atlas, Morocco: Field evaluation of the EG95 vaccine in sheep and cesticide treatment in dogs.
Journal
PLoS neglected tropical diseases
ISSN: 1935-2735
Titre abrégé: PLoS Negl Trop Dis
Pays: United States
ID NLM: 101291488
Informations de publication
Date de publication:
03 2021
03 2021
Historique:
received:
14
09
2020
accepted:
18
02
2021
revised:
18
03
2021
pubmed:
9
3
2021
medline:
6
7
2021
entrez:
8
3
2021
Statut:
epublish
Résumé
Cystic echinococcosis (CE) is an important cause of human morbidity and mortality worldwide, particularly in Morocco and other North African countries. We investigated the potential of three strategies to reduce Echinococcus granulosus transmission: (1) 4-monthly treatment of dogs with praziquantel, (2) vaccination of sheep with the EG95 vaccine and (3) a combination of both measures. These measures were implemented during four consecutive years in different areas of the Middle Atlas Mountains in Morocco. The outcome of the interventions was assessed through hydatid cyst (viable and non-viable) counts in liver and lungs using necropsy or in vivo ultrasound examination of the liver. A total of 402 lambs were recruited for annual vaccination with the EG95 anti-E. granulosus vaccine and 395 similar lambs were selected as non-vaccinated controls. At approximately four years of age the relative risk (estimated as odds ratio) for vaccinated sheep to have viable hydatid cysts compared with non-vaccinated controls was 3% (9.37% of the vaccinated sheep were found infected while 72.82% of the controls were infected; p = 0.002). The number of viable cysts in vaccinated animals was reduced by approximately 97% (mean counts were 0.28 and 9.18 respectively; p<0.001). An average of 595 owned dogs received 4-monthly treatment during the 44 months trial, corresponding to 91% of the owned dog population. Approximately, 5% of them were examined for E. granulosus adult worms by arecoline purge or eggs in feces (confirmed by PCR). The proportion of infected dogs significantly decreased after treatment (12% versus 35%; p<0.001). Post-treatment incidence of re-infestation corresponded to a monthly risk of 4% (95% CI: 3-6%). Treatment of owned dogs on a 4-monthly basis did not reduce the level of transmission of E. granulosus to sheep, nor did it enhance the level of control generated by vaccination of sheep with EG95, possibly because of unowned dogs and wild canids were not treated. These data suggest that vaccination of sheep with EG95 has the potential to reduce the level of CE in Morocco and in other parts of the world with similar transmission dynamics. Under the epidemiological circumstances existing in the trial area, 4-monthly treatment of owned dogs with praziquantel was insufficient to have a major impact of E. granulosus transmission to sheep.
Sections du résumé
BACKGROUND
Cystic echinococcosis (CE) is an important cause of human morbidity and mortality worldwide, particularly in Morocco and other North African countries.
METHODOLOGY/PRINCIPAL FINDINGS
We investigated the potential of three strategies to reduce Echinococcus granulosus transmission: (1) 4-monthly treatment of dogs with praziquantel, (2) vaccination of sheep with the EG95 vaccine and (3) a combination of both measures. These measures were implemented during four consecutive years in different areas of the Middle Atlas Mountains in Morocco. The outcome of the interventions was assessed through hydatid cyst (viable and non-viable) counts in liver and lungs using necropsy or in vivo ultrasound examination of the liver. A total of 402 lambs were recruited for annual vaccination with the EG95 anti-E. granulosus vaccine and 395 similar lambs were selected as non-vaccinated controls. At approximately four years of age the relative risk (estimated as odds ratio) for vaccinated sheep to have viable hydatid cysts compared with non-vaccinated controls was 3% (9.37% of the vaccinated sheep were found infected while 72.82% of the controls were infected; p = 0.002). The number of viable cysts in vaccinated animals was reduced by approximately 97% (mean counts were 0.28 and 9.18 respectively; p<0.001). An average of 595 owned dogs received 4-monthly treatment during the 44 months trial, corresponding to 91% of the owned dog population. Approximately, 5% of them were examined for E. granulosus adult worms by arecoline purge or eggs in feces (confirmed by PCR). The proportion of infected dogs significantly decreased after treatment (12% versus 35%; p<0.001). Post-treatment incidence of re-infestation corresponded to a monthly risk of 4% (95% CI: 3-6%). Treatment of owned dogs on a 4-monthly basis did not reduce the level of transmission of E. granulosus to sheep, nor did it enhance the level of control generated by vaccination of sheep with EG95, possibly because of unowned dogs and wild canids were not treated.
CONCLUSIONS/SIGNIFICANCE
These data suggest that vaccination of sheep with EG95 has the potential to reduce the level of CE in Morocco and in other parts of the world with similar transmission dynamics. Under the epidemiological circumstances existing in the trial area, 4-monthly treatment of owned dogs with praziquantel was insufficient to have a major impact of E. granulosus transmission to sheep.
Identifiants
pubmed: 33684115
doi: 10.1371/journal.pntd.0009253
pii: PNTD-D-20-01653
pmc: PMC7971873
doi:
Substances chimiques
Antigens, Helminth
0
EG95 protein, Echinococcus granulosus
0
Helminth Proteins
0
Praziquantel
6490C9U457
Types de publication
Journal Article
Research Support, Non-U.S. Gov't
Langues
eng
Sous-ensembles de citation
IM
Pagination
e0009253Déclaration de conflit d'intérêts
The authors have declared that no competing interests exist.
Références
Vet Res Commun. 2009 Sep;33 Suppl 1:47-52
pubmed: 19575305
Parasite Immunol. 2013 Feb;35(2):99-102
pubmed: 23009356
Parasitol Res. 2003 Oct;91(4):316-20
pubmed: 14574562
Zoonoses Public Health. 2019 Dec;66(8):889-899
pubmed: 31529690
Exp Parasitol. 2004 Mar-Apr;106(3-4):183-6
pubmed: 15172227
Iran J Parasitol. 2017 Oct-Dec;12(4):614-621
pubmed: 29317887
J Biosoc Sci. 2016 Sep;48 Suppl 1:S92-S115
pubmed: 27428068
Parasite. 2014;21:64
pubmed: 25456565
Korean J Parasitol. 2019 Oct;57(5):549-552
pubmed: 31715699
Parasitol Int. 2006;55 Suppl:S197-202
pubmed: 16337429
Vet Parasitol. 2010 Nov 24;174(1-2):2-11
pubmed: 20888694
Acta Trop. 2003 Feb;85(2):133-43
pubmed: 12606090
BMC Public Health. 2019 Jan 28;19(1):118
pubmed: 30691432
Parasit Vectors. 2019 Dec 27;12(1):606
pubmed: 31881913
PLoS Negl Trop Dis. 2017 Mar 1;11(3):e0005384
pubmed: 28248960
Trans R Soc Trop Med Hyg. 2001 Jul-Aug;95(4):379-83
pubmed: 11579878
Parasite Immunol. 1996 Sep;18(9):457-62
pubmed: 9226681
Vet Rec Open. 2014 Feb 04;1(1):e000004
pubmed: 26392870
Mol Biotechnol. 2011 Jul;48(3):277-89
pubmed: 21222242
Parasitology. 2003;127 Suppl:S143-58
pubmed: 15027611
Vet Parasitol. 2006 Apr 15;137(1-2):83-93
pubmed: 16473466
Vet Parasitol. 2007 Apr 30;145(3-4):297-303
pubmed: 17289266
Parasitology. 2006;133 Suppl:S27-42
pubmed: 17274847
J Vet Pharmacol Ther. 2019 Sep;42(5):497-504
pubmed: 31183888
Acta Trop. 2013 Aug;127(2):143-51
pubmed: 23632258
Med Mal Infect. 2020 Jan 9;:
pubmed: 31928912
Adv Parasitol. 2006;61:443-508
pubmed: 16735171
Vector Borne Zoonotic Dis. 2020 Jun;20(6):436-443
pubmed: 32077790
Parasitol Int. 2006;55 Suppl:S253-8
pubmed: 16364679
J Parasit Dis. 2019 Dec;43(4):560-565
pubmed: 31749525
Adv Parasitol. 2017;96:55-158
pubmed: 28212791
Int J Parasitol. 2014 Jan;44(1):9-18
pubmed: 24269720