BALB/c mice infection with hybrid Leishmania (V.) guyanensis/L. (V.) shawi showed an intermediate virulence profile compared to parental species infections.

IF 4.8 2区 医学 Q2 IMMUNOLOGY
Frontiers in Cellular and Infection Microbiology Pub Date : 2025-09-11 eCollection Date: 2025-01-01 DOI:10.3389/fcimb.2025.1648268
Ana Carolina Stocco Lima, Thaise Yumie Tomokane, Gabriela Fernandes Rodrigues, Larissa Dos Santos Alcântara, Marliane Batista Campos, Maíra Pombo, Márcia Dalastra Laurenti, Vania Lucia Ribeiro da Matta, Lucile Maria Floeter-Winter, Carlos Eduardo Pereira Corbett, Fernando Tobias Silveira, Cláudia Maria de Castro Gomes
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引用次数: 0

Abstract

Introduction: Hybridization events within the genus Leishmania have been documented; however, their impact on the infection dynamics of hybrids remains poorly understood. In this study, we compared the infection dynamics caused by a hybrid parasite, Leishmania (Viannia) guyanensis/Leishmania (Viannia) shawi, with those caused by its parental species, Leishmania (Viannia) guyanensis and Leishmania (Viannia) shawi, in BALB/c mice.

Methods: Balb/c mice were inoculated with stationary-phase promastigote forms of each parasite. Lesion development and parasite load were monitored longitudinally, and cytokine production was assessed at 35 days post-infection (PI).

Results: The infection with the hybrid parasite induced a more rapid and evident progression, attaining its largest dimension between days 14 and 28 days PI, followed by regression. In contrast, infection with L. (V.) guyanensis resulted in a continuous increase in swelling, whereas L. (V.) shawi caused only mild swelling. Parasite loads in skin and lymph nodes were comparable across groups, though the hybrid parasite exhibited a significant increase in parasite burden from day 35 PI onwards.

Discussion: The immunologic response of hybrid parasite infection was associated with reduced gamma interferon (IFN-γ) and elevated interleukin 4 (IL-4) production compared to parental species and controls (P < 0.05), with no significant differences observed in interleukin 12 (IL-12p40) or interleukin 10 (IL-10). Infection with L. (V.) guyanensis led to decreased IFN-γ in lymph nodes and increased IL-4 production in both skin and lymph nodes, whereas L. (V.) shawi infection did not significantly alter cytokine profiles.

Conclusion: Together, these findings provide important insights into the distinct biological behavior of the Leishmania hybrid parasite and its parental species, underscoring the relevance of hybridization in shaping host-parasite interactions and advancing our understanding of leishmaniasis within complex eco-epidemiological settings.

混合利什曼原虫感染BALB/c小鼠。与亲本种感染相比,(V.) shawi表现出中等毒力。
介绍:利什曼属内的杂交事件已被记录;然而,它们对杂交种感染动力学的影响仍然知之甚少。在本研究中,我们比较了一种杂交寄生虫——古雁利什曼原虫/沙威利什曼原虫及其亲本种古雁利什曼原虫和沙威利什曼原虫对BALB/c小鼠的感染动态。方法:Balb/c小鼠分别接种静止期各寄生虫原体。纵向监测病变发展和寄生虫负荷,并在感染后35天评估细胞因子的产生。结果:杂交寄生虫侵染后病情发展迅速、明显,在感染后第14 ~ 28天达到最大,随后逐渐消退。与此相反,感染古yanl . (V.) ensis导致肿胀持续增加,而L. (V.) shawi仅引起轻度肿胀。皮肤和淋巴结中的寄生虫负荷在各组之间具有可比性,尽管杂交寄生虫从第35天起寄生虫负荷显著增加。讨论:与亲本物种和对照相比,杂交寄生虫感染的免疫反应与γ干扰素(IFN-γ)减少和白细胞介素4 (IL-4)产生升高有关(P < 0.05),白细胞介素12 (IL-12p40)或白细胞介素10 (IL-10)没有显著差异。guyanensis感染导致淋巴结IFN-γ减少,皮肤和淋巴结IL-4产生增加,而L. (V.) shawi感染没有显著改变细胞因子谱。结论:总之,这些发现为利什曼原虫及其亲本物种的独特生物学行为提供了重要见解,强调了杂交在形成宿主-寄生虫相互作用中的相关性,并促进了我们在复杂的生态流行病学环境中对利什曼病的理解。
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来源期刊
CiteScore
7.90
自引率
7.00%
发文量
1817
审稿时长
14 weeks
期刊介绍: Frontiers in Cellular and Infection Microbiology is a leading specialty journal, publishing rigorously peer-reviewed research across all pathogenic microorganisms and their interaction with their hosts. Chief Editor Yousef Abu Kwaik, University of Louisville is supported by an outstanding Editorial Board of international experts. This multidisciplinary open-access journal is at the forefront of disseminating and communicating scientific knowledge and impactful discoveries to researchers, academics, clinicians and the public worldwide. Frontiers in Cellular and Infection Microbiology includes research on bacteria, fungi, parasites, viruses, endosymbionts, prions and all microbial pathogens as well as the microbiota and its effect on health and disease in various hosts. The research approaches include molecular microbiology, cellular microbiology, gene regulation, proteomics, signal transduction, pathogenic evolution, genomics, structural biology, and virulence factors as well as model hosts. Areas of research to counteract infectious agents by the host include the host innate and adaptive immune responses as well as metabolic restrictions to various pathogenic microorganisms, vaccine design and development against various pathogenic microorganisms, and the mechanisms of antibiotic resistance and its countermeasures.
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