» Articles » PMID: 28754151

Identification of Anaplasma Ovis Appendage-associated Protein (AAAP) for Development of an Indirect ELISA and Its Application

Overview
Journal Parasit Vectors
Publisher Biomed Central
Date 2017 Jul 30
PMID 28754151
Citations 4
Authors
Affiliations
Soon will be listed here.
Abstract

Background: Ovine anaplasmosis is a tick-borne disease that is caused by Anaplasma ovis in sheep and goats. The pathogen is widely distributed in tropical and subtropical regions of the world. At present, diagnosis of the disease mainly depends on microscopy or nucleic acid based molecular tests, although a few serological tests have been applied for the detection of A. ovis infection.

Results: Here we describe the identification of an A. ovis protein that is homologous to the A. marginale appendage-associated protein (AAAP). We expressed a recombinant fragment of this protein for the development of an indirect enzyme-linked immunosorbent assay (ELISA) for the detection of A. ovis. Anaplasma ovis-positive serum showed specific reactivity to recombinantly expressed AAAP (rAAAP), which was further confirmed by the rAAAP ELISA, which also demonstrated no cross-reactivity with sera from animals infected with A. bovis or other related pathogens in sheep and goats. Testing antibody kinetics of five experimentally infected sheep for 1 year demonstrated that the rAAAP ELISA is suitable for the detection of early and persistent infection of A. ovis infections. Investigation of 3138 field-collected serum samples from 54 regions in 23 provinces in China demonstrated that the seroprevalence varied from 9.4% to 65.3%, which is in agreement with previous reports of A. ovis infection.

Conclusions: An A. ovis derived antigenic protein, AAAP, was identified and the antigenicity of the recombinant AAAP was confirmed. Using rAAAP an indirect ELISA assay was established, and the assay has been proven to be an alternative serological diagnostic tool for investigating the prevalence of ovine anaplasmosis of sheep and goats.

Citing Articles

Long-lasting infection with Anaplasma ovis in sheep.

Ruiz H, de Arcaute M, Benito A, Villanueva-Saz S, Jimenez J, Lacasta D Vet Res Commun. 2023; 48(1):521-525.

PMID: 37528260 PMC: 10810980. DOI: 10.1007/s11259-023-10186-y.


Epidemiological Study Related to the First Outbreak of Ovine Anaplasmosis in Spain.

Lacasta D, Lorenzo M, Gonzalez J, de Arcaute M, Benito A, Baselga C Animals (Basel). 2021; 11(7).

PMID: 34359164 PMC: 8300400. DOI: 10.3390/ani11072036.


Clinical signs, prevalence, and hematobiochemical profiles associated with infections in sheep of North Iraq.

Abdullah D, Ali F, Jasim A, Ola-Fadunsin S, Gimba F, Ali M Vet World. 2020; 13(8):1524-1527.

PMID: 33061222 PMC: 7522931. DOI: 10.14202/vetworld.2020.1524-1527.


The Anaplasma ovis genome reveals a high proportion of pseudogenes.

Liu Z, Peasley A, Yang J, Li Y, Guan G, Luo J BMC Genomics. 2019; 20(1):69.

PMID: 30665414 PMC: 6341658. DOI: 10.1186/s12864-018-5374-6.

References
1.
Friedhoff K . Tick-borne diseases of sheep and goats caused by Babesia, Theileria or Anaplasma spp. Parassitologia. 1997; 39(2):99-109. View

2.
FRENCH D, Mcelwain T, McGuire T, Palmer G . Expression of Anaplasma marginale major surface protein 2 variants during persistent cyclic rickettsemia. Infect Immun. 1998; 66(3):1200-7. PMC: 108034. DOI: 10.1128/IAI.66.3.1200-1207.1998. View

3.
Yin H, Lu W, Luo J . Babesiosis in China. Trop Anim Health Prod. 1998; 29(4 Suppl):11S-15S. DOI: 10.1007/BF02632908. View

4.
KRIER J, Ristic M . Anaplasmosis. VII. Experimental Anaplasma ovis infection in white-tailed deer (Dama virginiana). Am J Vet Res. 1963; 24:567-72. View

5.
Yin H, Liu Z, Guan G, Liu A, Ma M, Ren Q . Detection and differentiation of Theileria luwenshuni and T. uilenbergi infection in small ruminants by PCR. Transbound Emerg Dis. 2008; 55(5-6):233-7. DOI: 10.1111/j.1865-1682.2008.01031.x. View