Hantavirus Infection: Contemporary Concepts in Microbiology, Pathogenesis, Gut Microbial Interactions, Diagnosis, and Management
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Hantaviruses are globally distributed zoonotic negative-sense single-stranded RNA viruses responsible for hemorrhagic fever with renal syndrome (HFRS) and hantavirus pulmonary syndrome (HPS), also termed hantavirus cardiopulmonary syndrome. Human infection occurs predominantly through inhalation of aerosolized rodent saliva, urine, or feces contaminated with hantaviruses. Compared with the general population, infected individuals exhibit markedly increased risks of endothelial dysfunction, capillary leakage, thrombocytopenia, acute kidney injury, pulmonary edema, cardiogenic shock, cytokine storm, and multisystem inflammatory failure. Although rodent-to-human transmission remains the principal route of infection, Andes virus has demonstrated limited human-to-human transmission.
The pathogenesis of hantavirus infection involves endothelial invasion, dysregulated innate and adaptive immune activation, cytokine-mediated vascular injury, complement activation, coagulation abnormalities, and inflammatory endothelial dysfunction. Viral glycoproteins facilitate cellular attachment through β3 integrins, protocadherin-1, and other endothelial receptors, promoting viral entry and systemic dissemination. Recent evidence additionally suggests that gut microbial dysbiosis, intestinal barrier dysfunction, and microbial translocation may amplify systemic inflammation through the gut–lung and gut–immune axes.
Clinically, hantavirus infection presents with highly variable manifestations ranging from mild febrile illness to fulminant respiratory failure, hemorrhage, renal dysfunction, and circulatory collapse. Diagnosis relies upon epidemiological exposure history, serological testing, reverse transcription polymerase chain reaction, and supportive laboratory findings. Current management remains primarily supportive and includes hemodynamic stabilization, oxygen therapy, mechanical ventilation, renal replacement therapy, and extracorporeal membrane oxygenation in severe disease.
This descriptive review summarizes the contemporary understanding of hantavirus microbiology, epidemiology, pathogenesis, gut microbial interactions, clinical manifestations, diagnosis, differential diagnosis, treatment strategies, prognosis, limitations, and future directions while emphasizing the significant inflammatory and vascular burden associated with hantavirus disease compared with the general population.
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References
- [1]. Mittler E, Dieterle ME, Kleinfelter LM, Slough MM, Chandran K, Jangra RK. Hantavirus entry: Perspectives and recent advances. Adv Virus Res. 2019;104:185-224. doi: 10.1016/bs.aivir.2019.07.002. Epub 2019 Aug 7. PMID: 31439149; PMCID: PMC6881143.
- [2]. Vaheri A, Strandin T, Hepojoki J, Sironen T, Henttonen H, Mäkelä S, et al. Uncovering the mysteries of hantavirus infections. Nat Rev Microbiol. 2013;11(8):539-550.
- [3]. Vial PA, Ferrés M, Vial C, Klingström J, Ahlm C, López R, et al. Hantavirus in humans: a review of clinical aspects and management. Lancet Infect Dis. 2023;23(9):e371-e382.
- [4]. Munir N, Jahangeer M, Hussain S, Mahmood Z, Ashiq M, Ehsan F, et al. Hantavirus diseases pathophysiology, their diagnostic strategies and therapeutic approaches: A review. Clin Exp Pharmacol Physiol. 2021;48(1):20-34.
- [5]. Witkowski PT, Perley CC, Brocato RL, Hooper JW, Jääskeläinen AJ, Plyusnin A. What do we know about how hantaviruses interact with their different hosts? Viruses. 2016;8(8):223.
- [6]. Martínez-Valdebenito C, Calvo M, Vial C, Mansilla R, Marco C, Palma RE, et al. Evidence for human-to-human transmission of hantavirus: A systematic review. J Infect Dis. 2022;226(8):1362-1371.
- [7]. Witkowski PT, Perley CC, Brocato RL, Hooper JW, Jürgensen C, Schulzke JD, Krüger DH, Bücker R. Gastrointestinal Tract As Entry Route for Hantavirus Infection. Front Microbiol. 2017 Sep 8;8:1721. doi: 10.3389/fmicb.2017.01721. PMID: 28943870; PMCID: PMC5596106.
- [8]. Xiong, Y.; Dai, Z.; He, F.; Liu, R.; Wang, J.; Zhan, Z.; Jia, H.; Chen, S.; Cai, L. Effect of Hantavirus Infection on the Rodent Lung Microbiome: Specific Regulatory Roles of Host Species and Virus Types. Microorganisms 2026, 14, 244. https://doi.org/10.3390/microorganisms14010244
- [9]. WASIAK, Jakub, ZIELONKA, Kacper, DĄDELA, Bartosz, MARKOWSKI, Marcin, ŚLIWA, Natalia, MAJEWSKA, Emilia Maria, KAWALSKA, Eliza, GNITECKI, Szymon, JANCZURA, Szymon and BOROWSKI, Maciej. Gut Microbiota and Gut-Brain Axis in Health and Disease A Narrative Review. Quality in Sport. Online. 11 May 2025. Vol. 41, p. 60102. [Accessed 21 May 2026]. DOI 10.12775/QS.2025.41.60102.
- [10]. Crnčević, N.; Rifatbegović, Z.; Hukić, M.; Deumić, S.; Pramenković, E.; Selimagić, A.; Gavrankapetanović, I.; Avdić, M. Atypical Viral Infections in Gastroenterology. Diseases 2022, 10, 87. https://doi.org/10.3390/diseases10040087
- [11]. Pronovost GN, Yu K, Elena, Sucheta Telang, Chen AS, Vuong HE, et al. The maternal microbiome promotes placental development in mice. Science Advances. 2023 Oct 6;9(40).
- [12]. Liu Y, Yan D, Chen R, Zhang Y, Wang C, Qian G. Recent insights and advances in gut microbiota's influence on host antiviral immunity. Front Microbiol. 2025 Feb 27;16:1536778. doi: 10.3389/fmicb.2025.1536778. PMID: 40083779; PMCID: PMC11903723.
- [13]. Kazemifard N, Dehkohneh A, Baradaran Ghavami S. Probiotics and probiotic-based vaccines: A novel approach for improving vaccine efficacy. Front Med (Lausanne). 2022 Oct 13;9:940454. doi: 10.3389/fmed.2022.940454. PMID: 36313997; PMCID: PMC9606607.
- [14]. Stecher B. The Roles of Inflammation, Nutrient Availability and the Commensal Microbiota in Enteric Pathogen Infection. Microbiol Spectr. 2015 Jun;3(3). doi: 10.1128/microbiolspec.MBP-0008-2014. PMID: 26185088.
- [15]. Thomas LV, Ockhuizen T, Suzuki K. Exploring the influence of the gut microbiota and probiotics on health: a symposium report. Br J Nutr. 2014 Jul;112 Suppl 1(Suppl 1):S1-18. doi: 10.1017/S0007114514001275. PMID: 24953670; PMCID: PMC4077244.
- [16]. Sencio V, Machado MG, Trottein F. The lung-gut axis during viral respiratory infections: the impact of gut dysbiosis on secondary disease outcomes. Mucosal Immunol. 2021 Mar;14(2):296-304. doi: 10.1038/s41385-020-00361-8. Epub 2021 Jan 26. PMID: 33500564; PMCID: PMC7835650.
- [17]. Shahbazi R, Yasavoli-Sharahi H, Alsadi N, Ismail N, Matar C. Probiotics in Treatment of Viral Respiratory Infections and Neuroinflammatory Disorders. Molecules. 2020 Oct 22;25(21):4891. doi: 10.3390/molecules25214891. PMID: 33105830; PMCID: PMC7660077.
- [18]. Rastogi S, Mohanty S, Sharma S, Tripathi P. Possible role of gut microbes and host's immune response in gut-lung homeostasis. Front Immunol. 2022 Oct 4;13:954339. doi: 10.3389/fimmu.2022.954339. PMID: 36275735; PMCID: PMC9581402.
- [19]. Nie, J., Zhou, L., Tian, W. et al. Deep insight into cytokine storm: from pathogenesis to treatment. Sig Transduct Target Ther 10, 112 (2025). https://doi.org/10.1038/s41392-025-02178-y
- [20]. Xu, JQ., Zhang, WY., Fu, JJ. et al. Viral sepsis: diagnosis, clinical features, pathogenesis, and clinical considerations. Military Med Res 11, 78 (2024). https://doi.org/10.1186/s40779-024-00581-0