Theileria annulata infects B-cells in sheep, which display lower dissemination potential compared to T. lestoquardi-infected ovine B-cells

被引:0
作者
Tajeri, Shahin [1 ,2 ,3 ]
de Late, Perle Latre [2 ,3 ,5 ]
Hemmink, Johanneke D. [4 ,6 ]
Vrettou, Christina [4 ]
Langsley, Gordon [2 ,3 ]
Morrison, W. Ivan [4 ]
机构
[1] Free Univ Berlin, Inst Parasitol & Trop Vet Med, D-14163 Berlin, Germany
[2] Inst Cochin, Inserm U1016 CNRS UMR8104, Paris, France
[3] Univ Paris Descartes Sorbonne Paris Cite, Fac Med, Lab Biol Comparat Apicomplexes, Paris, France
[4] Univ Edinburgh, Roslin Inst, Royal Dick Sch Vet Sci, Edinburgh EH25 9RG, Scotland
[5] Univ Missouri, Christopher S Bond Life Sci Ctr, 1201 Rollins St, Columbia, MO 65211 USA
[6] Int Livestock Res Inst ILRI, POB 30709, Nairobi, Kenya
关键词
Theileria lestoquardi; Theileria annulata; Theileriosis; Leukocyte transformation; Sheep; IN-VITRO; MATRIX METALLOPROTEINASES; CROSS-IMMUNITY; UP-REGULATION; CATTLE; AP-1; TRANSCRIPTION; ATTENUATION; METASTASIS; EXPRESSION;
D O I
10.1016/j.ttbdis.2025.102443
中图分类号
R51 [传染病];
学科分类号
100401 ;
摘要
Theileria annulata and Theileria lestoquardi are deadly tick-borne parasites of cattle and sheep, respectively. These parasites are transmitted by Hyalomma ticks, and their geographical distributions partially overlap, with T. annulata having a wider range. Theileria lestoquardi infection is highly pathogenic in its natural sheep and goat hosts while T. annulata infection usually causes a mild disease in these species. Interestingly, T. annulata does not produce merozoites/piroplasms in sheep and goats, therefore it is not tick-transmissible. The aim of the current study was to understand the basis of the attenuated pathogenicity of ovine infections by T. annulata. Theileria annulata and T. lestoquardi sporozoites were used to infect sheep and parasitized ovine leukocytes were isolated and phenotyped. This revealed that T. annulata sporozites target ovine B-cells, whereas T. lestoquardi sporozoite infection was not restricted to ovine B-cells. The ability of ovine B-cells infected with T. lestoquardi or T. annulata to traverse Matrigel in vitro was investigated, as a surrogate for their ability to disseminate in vivo and cause disease. The Matrigel traversal index ofT. lestoquardi-transformed ovine B-cells was significantly higher than that of T. annulata-transformed ovine B-cells isolated from the same host, consistent with the reported diminished pathogenicity of T. annulata infections in sheep. Theileria lestoquardi-transformed ovine B-cells preferentially expressed matrix metalloproteinase 2 (mmp2), whereas T. annulata-infected ovine B-cells strongly expressed mmp9. Correspondingly, MMP9 protein levels and collagenase activity were higher in T. annulata-transformed ovine B-cells. However, T. annulata-transformed ovine B-cells expressed higher levels of transcripts for Tissue Inhibitor of Metallopeptidases 1 and 2 (TIMP1 and TIMP2). TIMPs are the natural endogenous inhibitors of MMPs. This argues that their heightened expression could underpin the significantly lower Matrigel traversal activity of T. annulata-infected compared to T. lestoquardi-infected ovine B-cells.
引用
收藏
页数:8
相关论文
共 47 条
  • [21] Goddeeris B.M., Morrison W.I., Techniques for the generation, cloning, and characterization of bovine cytotoxic T cells specific for the protozoan Theileria parva, J. Tissue Cult. Methods, 11, 2, pp. 101-110, (1988)
  • [22] Haidar M., Echebli N., Ding Y., Kamau E., Langsley G., Transforming growth factor β2 promotes transcription of COX2 and EP4, leading to a prostaglandin E2-driven autostimulatory loop that enhances virulence of Theileria annulata-transformed macrophages, Infect. Immun., 83, 5, pp. 1869-1880, (2015)
  • [23] Haidar M., Rchiad Z., Ansari H.R., Ben-Rached F., Tajeri S., Latre De Late P., Langsley G., Pain A., miR-126-5p by direct targeting of JNK-interacting protein-2 (JIP-2) plays a key role in Theileria-infected macrophage virulence, PLoS Pathog, 14, 3, (2018)
  • [24] Haidar M., Tajeri S., Momeux L., Mourier T., Ben-Rached F., Mfarrej S., Rchiad Z., Pain A., Langsley G., miR-34c-3p regulates protein kinase A activity independent of cAMP by dicing prkar2b transcripts in Theileria annulata-infected leukocytes, mSphere, 8, 2, (2023)
  • [25] Hall R., Ilhan T., Kirvar E., Wilkie G., Preston P.M., Darghouth M., Somerville R., Adamson R., Mechanism(s) of attenuation of Theileria annulata vaccine cell lines, Trop. Med. Int. Health, 4, 9, pp. A78-A84, (1999)
  • [26] Hooshmand-Rad P., The use of tissue culture attenuated live vaccine for Theileria hirci, Dev. Biol. Stand., 62, pp. 119-127, (1985)
  • [27] Jalali S.M., Jolodar A., Rasooli A., Darabifard A., Detection of Theileria lestoquardi cross infection in cattle with clinical theileriosis in Iran, Acta Parasitol, 61, 4, pp. 756-761, (2016)
  • [28] Leemans I., Brown D., Fossum C., Hooshmand-Rad P., Kirvar E., Wilkie G., Uggla A., Infectivity and cross-immunity studies of Theileria lestoquardi and Theileria annulata in sheep and cattle: II. In vitro studies, Vet. Parasitol., 82, 3, pp. 193-204, (1999)
  • [29] Leemans I., Brown D., Hooshmand-Rad P., Kirvar E., Uggla A., Infectivity and cross-immunity studies of Theileria lestoquardi and Theileria annulata in sheep and cattle: I. In vivo responses, Vet. Parasitol., 82, 3, pp. 179-192, (1999)
  • [30] Leemans I., Fossum C., Johannisson A., Hooshmand-Rad P., Comparative studies on surface phenotypes of Theileria lestoquardi and T. annulata schizont-infected cells, Parasitol. Res., 87, 9, pp. 768-777, (2001)