Leptospirosis.
Abstract: Leptospirosis is a zoonotic bacterial infection that is prevalent across all continents and is caused by pathogenic spirochaetes of the genus Leptospira. Although infection can be asymptomatic, symptomatic disease can vary in severity from mild to severe illness, the latter characterized by icterus and/or multi-organ dysfunction and potentially death. An estimated one million cases of leptospirosis occur globally each year, resulting in ~60,000 deaths. The pathogenesis of severe leptospirosis is poorly understood but is believed to involve an interplay between genetic predisposition, pathogen virulence and dysregulated immune responses that trigger a cytokine storm with associated immunoparesis. Leptospira are susceptible to several low-cost antibiotics, including benzyl penicillin, doxycycline, cephalosporins and macrolides, when used in the early phase of infection. Late disease with organ dysfunction is treated with supportive care, and the benefit of antibiotics during late disease is doubtful. Very few countries have licensed a vaccine for human leptospirosis, and available vaccines only protect against rodent-associated serogroups. Exposure control by behavioural modifications and personal protective measures are the major preventative measures in leptospirosis, and the efficacy of prophylactic antibiotics has not been confirmed in clinical trials. Future research is needed to accurately estimate leptospirosis disease burden across the globe, to understand the pathophysiology of severe leptospirosis to inform the design of targeted immunotherapies and vaccines, and to develop cost-effective and accurate point-of-care diagnostics.
© 2025. Springer Nature Limited.
Publication Date: 2025-05-02 PubMed ID: 40316520PubMed Central: 4442676DOI: 10.1038/s41572-025-00614-5Google Scholar: Lookup
The Equine Research Bank provides access to a large database of publicly available scientific literature. Inclusion in the Research Bank does not imply endorsement of study methods or findings by Mad Barn.
- Journal Article
- Review
Summary
This research summary has been generated with artificial intelligence and may contain errors and omissions. Refer to the original study to confirm details provided. Submit correction.
This research article primarily discusses the connection between the disease Leptospirosis and ocular changes in horses, including the recurrent sequelae of these changes. The research also explores the more recent increase in reports of equine abortion, stillbirth, and neonatal disease associated with this infection and potential treatments to be used.
Disease and its effects
- The research starts by discussing how clinical leptospirosis in horses is primarily connected to changes in the horse’s eyes, more specifically uveitis and recurrent sequelae, or the aftereffects of these ocular changes. Sequelae are typically pathological conditions resulting from a disease or injury.
- While there have been sporadic reports of kidney and liver involvement in horses due to this disease, these are less common.
Emerging Concerns
- In recent times, a type of leptospira called serovar bratislava has been found to be adapted in horses, which is significant for the study of the disease in this species.
- Reports on equine abortion and stillbirth have become more frequent. This frequency is likely due to improved diagnostic techniques, rather than a rise in the disease itself.
- Particularly noteworthy is the increasing recognition of equine neonatal disease circumstance associated with leptospira infection.
- Whether the infection causes abortion or affects foals (young horses) may depend on the stage of gestation when the mare is exposed and the immune status of the host (the mare, in this case).
Treatment Options
- The article then moves onto discussing the treatment options for this condition. The choice of antibiotic for treating equine leptospirosis is uncertain because specific studies focused on equine have not yet been conducted.
- That said, treatments used for other species suggest that streptomycin might be a good therapeutic choice for the chronic shedding state (where the bacteria is persistently released in the urine).
- Streptomycin may also be used in combination with other antimicrobials for treating acute (short-term but severe) disease.
- Furthermore, Penicillins (specifically potentiated ones) and tetracycline might be logical choices for treating acute leptospirosis, provided they are given in the appropriate or high-end dosages.
Cite This Article
APA
Rajapakse S, Fernando N, Dreyfus A, Smith C, Rodrigo C.
(2025).
Leptospirosis.
Nat Rev Dis Primers, 11(1), 32.
https://doi.org/10.1038/s41572-025-00614-5 Publication
Researcher Affiliations
- Department of Clinical Medicine, Faculty of Medicine, University of Colombo, Colombo, Sri Lanka. senaka@med.cmb.ac.lk.
- Institute of Biochemistry, Molecular Biology and Biotechnology, University of Colombo, Colombo, Sri Lanka.
- Section of Epidemiology, Vetsuisse Faculty, University of Zurich, Zurich, Switzerland.
- Department of Clinical Research, Faculty of Infectious and Tropical Diseases, London School of Hygiene and Tropical Medicine, London, UK.
- School of Tropical Medicine and Global Health, Nagasaki University, Nagasaki, Japan.
- Department of Pathology, School of Biomedical Sciences, Faculty of Medicine and Health, University of New South Wales, Sydney, New South Wales, Australia.
MeSH Terms
- Humans
- Leptospirosis / epidemiology
- Leptospirosis / physiopathology
- Leptospirosis / diagnosis
- Anti-Bacterial Agents / therapeutic use
- Anti-Bacterial Agents / pharmacology
- Animals
- Leptospira / pathogenicity
Conflict of Interest Statement
Competing interests: The authors declare no competing interests.
References
This article includes 249 references
- European Centre for Disease Prevention and Control. Factsheet about leptospirosis. 2017.
- Haake DA, Levett PN. Leptospirosis in humans. Curr. Top. Microbiol. Immunol. 387, 65–97 (2015).
- Bolin CA, Koellner P. Human-to-human transmission of Leptospira interrogans by milk. J. Infect. Dis. 158, 246–247 (1988).
- Carles G, Montoya E, Joly F, Peneau C. Leptospirosis and pregnancy. Eleven cases in French Guyana. J. Gynecol. Obstet. Biol. Reprod. 24, 418–421 (1995).
- Evangelista KV, Coburn J. Leptospira as an emerging pathogen: a review of its biology, pathogenesis and host immune responses. Future Microbiol. 5, 1413–1425 (2010).
- Raddi G et al. Three-dimensional structures of pathogenic and saprophytic leptospira species revealed by cryo-electron tomography. J. Bacteriol. 194, 1299–1306 (2012).
- Vincent AT et al. Revisiting the taxonomy and evolution of pathogenicity of the genus Leptospira through the prism of genomics. PLoS Negl. Trop. Dis. 13, e0007270 (2019).
- Kędzierska-Mieszkowska S. Sigma factors of RNA polymerase in the pathogenic spirochaete Leptospira interrogans, the causative agent of leptospirosis. FASEB J. 37, e23163 (2023).
- Guglielmini J et al. Genus-wide Leptospira core genome multilocus sequence typing for strain taxonomy and global surveillance. PLoS Negl. Trop. Dis. 13, e0007374 (2019).
- Costa F et al. Global morbidity and mortality of leptospirosis: a systematic review. PLoS Negl. Trop. Dis. 9, e0003898 (2015).
- Weil A. Ueber einer eigenhuemliche, mit milztumor, icterus un nephritis einhergehende, acute infektionskrankheit. Deutsch Arch. Klin. Med. 109, 209–232 (1886).
- Clemente BM, Pineda-Cortel MR, Villaflores O. Evaluating immunochromatographic test kits for diagnosis of acute human leptospirosis: a systematic review. Heliyon 8, e11829 (2022).
- Limmathurotsakul D et al. Fool’s gold: why imperfect reference tests are undermining the evaluation of novel diagnostics: a reevaluation of 5 diagnostic tests for leptospirosis. Clin. Infect. Dis. 55, 322–331 (2012).
- Rajapakse S, Rodrigo C, Handunnetti SM, Fernando SD. Current immunological and molecular tools for leptospirosis: diagnostics, vaccine design, and biomarkers for predicting severity. Ann. Clin. Microbiol. Antimicrob. 14, 2 (2015).
- Boss J et al. Antimicrobial susceptibility testing of leptospira spp. in the Lao People’s Democratic Republic using disk diffusion. Am. J. Trop. Med. Hyg. 100, 1073–1078 (2019).
- Chawla V, Trivedi TH, Yeolekar ME. Epidemic of leptospirosis: an ICU experience. J. Assoc. Physicians India 52, 619–622 (2004).
- Levett PN. Leptospirosis. Clin. Microbiol. Rev. 14, 296–326 (2001).
- Bharti AR et al. Leptospirosis: a zoonotic disease of global importance. Lancet Infect. Dis. 3, 757–771 (2003).
- Munoz-Zanzi C et al. A systematic literature review of leptospirosis outbreaks worldwide, 1970–2012. Rev. Panam. Salud Publica 44, e78 (2020).
- Zeng Z, Zhan J, Chen L, Chen H, Cheng S. Global, regional, and national dengue burden from 1990 to 2017: a systematic analysis based on the global burden of disease study 2017. eClinicalMedicine 2021.
- Allan KJ et al. Epidemiology of leptospirosis in Africa: a systematic review of a neglected zoonosis and a paradigm for ‘One Health’ in Africa. PLoS Negl. Trop. Dis. 9, e0003899 (2015).
- Gizamba JM, Mugisha L. Leptospirosis in humans and selected animals in sub-Saharan Africa, 2014–2022: a systematic review and meta-analysis. BMC Infect. Dis. 23, 649 (2023).
- Beauté J et al. Epidemiology of reported cases of leptospirosis in the EU/EEA, 2010 to 2021. Euro Surveill. 2024.
- Lau CL, Smythe LD, Craig SB, Weinstein P. Climate change, flooding, urbanisation and leptospirosis: fuelling the fire?. Trans. R. Soc. Trop. Med. Hyg. 104, 631–638 (2010).
- Cann KF, Thomas DR, Salmon RL, Wyn-Jones AP, Kay D. Extreme water-related weather events and waterborne disease. Epidemiol. Infect. 141, 671–686 (2013).
- Baharom M et al. Environmental and occupational factors associated with leptospirosis: a systematic review. Heliyon 10, e23473 (2024).
- Mwachui MA, Crump L, Hartskeerl R, Zinsstag J, Hattendorf J. Environmental and behavioural determinants of leptospirosis transmission: a systematic review. PLoS Negl. Trop. Dis. 9, e0003843 (2015).
- Hartskeerl RA, Collares-Pereira M, Ellis WA. Emergence, control and re-emerging leptospirosis: dynamics of infection in the changing world. Clin. Microbiol. Infect. 17, 494–501 (2011).
- Hagedoorn NN et al. Global distribution of Leptospira serovar isolations and detections from animal host species: a systematic review and online database. Trop. Med. Int. Health 29, 161–172 (2024).
- Allan KJ et al. Assessment of animal hosts of pathogenic Leptospira in northern Tanzania. PLoS Negl. Trop. Dis. 12, e0006444 (2018).
- Chadsuthi S et al. Investigation on predominant Leptospira serovars and its distribution in humans and livestock in Thailand, 2010–2015. PLoS Negl. Trop. Dis. 11, e0005228 (2017).
- Casanovas-Massana A et al. Genetic evidence for a potential environmental pathway to spillover infection of rat-borne leptospirosis. J. Infect. Dis. 225, 130–134 (2022).
- Faine S, Adler B, Bolin C, Perolat P. Leptospira and Leptospirosis Vol. 2. 1999.
- Adler B, de la Pena Moctezuma A. Leptospira and leptospirosis. Vet. Microbiol. 140, 287–296 (2010).
- Bierque E, Thibeaux R, Girault D, Soupé-Gilbert M-E, Goarant C. A systematic review of Leptospira in water and soil environments. PLoS ONE 15, e0227055 (2020).
- Thibeaux R et al. Seeking the environmental source of Leptospirosis reveals durable bacterial viability in river soils. PLoS Negl. Trop. Dis. 11, e0005414 (2017).
- Hacker KP et al. Influence of rainfall on leptospira infection and disease in a tropical urban setting, Brazil. Emerg. Infect. Dis. 26, 311–314 (2020).
- Rodríguez-Rodríguez V et al. Acute human leptospirosis in a Caribbean region of Colombia: from classic to emerging risk factors. Zoonoses Public Health 71, 107–119 (2024).
- Susanna D, Nova RIT, Rozek L. Community behaviors that affect the incidence of leptospirosis in West Jakarta, Indonesia. Vector Borne Zoonotic Dis. 23, 29–34 (2023).
- Amilasan AS et al. Outbreak of leptospirosis after flood, the Philippines, 2009. Emerg. Infect. Dis. 18, 91–94 (2012).
- Sanders EJ et al. Increase of leptospirosis in dengue-negative patients after a hurricane in Puerto Rico in 1996 (correction of 1966). Am. J. Trop. Med. Hyg. 61, 399–404 (1999).
- Dreesman J et al. Investigation and response to a large outbreak of leptospirosis in field workers in Lower Saxony, Germany. Zoonoses Public Health 70, 315–326 (2023).
- Dreyfus A et al. Risk factors for new infection with Leptospira in meat workers in New Zealand. Occup. Environ. Med. 72, 219–225 (2015).
- Pagès F et al. Investigation of a leptospirosis outbreak in triathlon participants, Réunion Island, 2013. Epidemiol. Infect. 144, 661–669 (2016).
- Bradley EA, Lockaby G. Leptospirosis and the environment: a review and future directions. Pathogens 2023.
- Magalhães AR et al. Neglected tropical diseases risk correlates with poverty and early ecosystem destruction. Infect. Dis. Poverty 12, 32 (2023).
- Jeffree MS et al. High incidence of asymptomatic leptospirosis among urban sanitation workers from Kota Kinabalu, Sabah, Malaysian Borneo. Sci. Rep. 10, 19442 (2020).
- Khalil H et al. Poverty, sanitation, and Leptospira transmission pathways in residents from four Brazilian slums. PLoS Negl. Trop. Dis. 15, e0009256 (2021).
- Reis RB et al. Impact of environment and social gradient on Leptospira infection in urban slums. PLoS Negl. Trop. Dis. 2, e228 (2008).
- Antima, Banerjee S. Modeling the dynamics of leptospirosis in India. Sci. Rep. 13, 19791 (2023).
- Lingappa J et al. HLA-DQ6 and ingestion of contaminated water: possible gene–environment interaction in an outbreak of Leptospirosis. Genes Immun. 5, 197–202 (2004).
- Agampodi SB, Matthias MA, Moreno AC, Vinetz JM. Utility of quantitative polymerase chain reaction in leptospirosis diagnosis: association of level of leptospiremia and clinical manifestations in Sri Lanka. Clin. Infect. Dis. 54, 1249–1255 (2012).
- Cagliero J, Villanueva S, Matsui M. Leptospirosis pathophysiology: into the storm of cytokines. Front. Cell. Infect. Microbiol. 8, 204 (2018).
- Nicodemo AC et al. Lung lesions in human leptospirosis: microscopic, immunohistochemical, and ultrastructural features related to thrombocytopenia. Am. J. Trop. Med. Hyg. 56, 181–187 (1997).
- Chierakul W et al. Activation of the coagulation cascade in patients with leptospirosis. Clin. Infect. Dis. 46, 254–260 (2008).
- Yücel Koçak S, Kudu A, Kayalar A, Yilmaz M, Apaydin S. Leptospirosis with acute renal failure and vasculitis: a case report. Arch. Rheumatol. 34, 229–232 (2019).
- De Brito T, Silva A, Abreu PAE. Pathology and pathogenesis of human leptospirosis: a commented review. Rev. Inst. Med. Trop. Sao Paulo 60, e23 (2018).
- Shintaku M, Itoh H, Tsutsumi Y. Weil’s disease (leptospirosis) manifesting as fulminant hepatic failure: report of an autopsy case. Pathol. Res. Pract. 210, 1134–1137 (2014).
- Arean VM. The pathologic anatomy and pathogenesis of fatal human leptospirosis (Weil’s disease). Am. J. Pathol. 40, 393–423 (1962).
- Sitprija V, Evans H. The kidney in human leptospirosis. Am. J. Med. 49, 780–788 (1970).
- Abdulkader RC, Silva MV. The kidney in leptospirosis. Pediatr. Nephrol. 23, 2111–2120 (2008).
- Dolhnikoff M, Mauad T, Bethlem EP, Carvalho CR. Pathology and pathophysiology of pulmonary manifestations in leptospirosis. Braz. J. Infect. Dis. 11, 142–148 (2007).
- Fernando T et al. Electrocardiographic and echocardiographic manifestations of cardiac involvement in leptospirosis. Trans. R. Soc. Trop. Med. Hyg. 107, 457–459 (2013).
- Swarath S et al. Leptospirosis-induced myocarditis and arrhythmias. J. Investig. Med. High. Impact Case Rep. 11, 23247096231179450 (2023).
- Silva JJ et al. Clinicopathological and immunohistochemical features of the severe pulmonary form of leptospirosis. Rev. Soc. Bras. Med. Trop. 35, 395–399 (2002).
- Cédola M et al. Association of Toll-like receptor 2 Arg753Gln and Toll-like receptor 1 Ile602Ser single-nucleotide polymorphisms with leptospirosis in an Argentine population. Acta Trop. 146, 73–80 (2015).
- Viriyakosol S, Matthias MA, Swancutt MA, Kirkland TN, Vinetz JM. Toll-like receptor 4 protects against lethal Leptospira interrogans serovar icterohaemorrhagiae infection and contributes to in vivo control of leptospiral burden. Infect. Immun. 74, 887–895 (2006).
- Haake DA, Zückert WR. Spirochetal lipoproteins in pathogenesis and immunity. Curr. Top. Microbiol. Immunol. 415, 239–271 (2018).
- Li D, Wu M. Pattern recognition receptors in health and diseases. Signal. Transduct. Target. Ther. 6, 291 (2021).
- Senavirathna I, Rathish D, Agampodi S. Cytokine response in human leptospirosis with different clinical outcomes: a systematic review. BMC Infect. Dis. 20, 268 (2020).
- Wang H et al. Leptospiral hemolysins induce proinflammatory cytokines through Toll-like receptor 2-and 4-mediated JNK and NF-κB signaling pathways. PLoS ONE 7, e42266 (2012).
- Reis EA et al. Cytokine response signatures in disease progression and development of severe clinical outcomes for leptospirosis. PLoS Negl. Trop. Dis. 7, e2457 (2013).
- Nisansala T et al. Contributing role of TNF, IL-10, sTNFR1 and TNF gene polymorphisms in disease severity of leptospirosis. Med. Microbiol. Immunol. 210, 211–219 (2021).
- Hsu SH et al. Peptidoglycan mediates Leptospira outer membrane protein Loa22 to toll-like receptor 2 for inflammatory interaction: a novel innate immune recognition. Sci. Rep. 11, 1064 (2021).
- Schuler EJA, Patel DT, Marconi RT. The leptospiral OmpA-like protein (Loa22) is a surface-exposed antigen that elicits bactericidal antibody against heterologous Leptospira. Vaccine X 15, 100382 (2023).
- Wang B, Sullivan JA, Sullivan GW, Mandell GL. Role of specific antibody in interaction of leptospires with human monocytes and monocyte-derived macrophages. Infect. Immun. 46, 809–813 (1984).
- Li S et al. Replication or death: distinct fates of pathogenic Leptospira strain Lai within macrophages of human or mouse origin. Innate Immun. 16, 80–92 (2010).
- Eshghi A et al. Leptospira interrogans catalase is required for resistance to H2O2 and for virulence. Infect. Immun. 80, 3892–3899 (2012).
- Fernando N et al. Protein carbonyl as a biomarker of oxidative stress in severe leptospirosis, and its usefulness in differentiating leptospirosis from dengue infections. PLoS ONE 11, e0156085 (2016).
- Wang B, Sullivan J, Sullivan GW, Mandell GL. Interaction of leptospires with human polymorphonuclear neutrophils. Infect. Immun. 44, 459–464 (1984).
- Vieira ML et al. Leptospira interrogans outer membrane protein LipL21 is a potent inhibitor of neutrophil myeloperoxidase. Virulence 9, 414–425 (2018).
- Aratani Y. Myeloperoxidase: its role for host defense, inflammation, and neutrophil function. Arch. Biochem. Biophys. 640, 47–52 (2018).
- Jost BH, Adler B, Vinh T, Faine S. A monoclonal antibody reacting with a determinant on leptospiral lipopolysaccharide protects guinea pigs against leptospirosis. J. Med. Microbiol. 22, 269–275 (1986).
- Rees EM et al. Estimating the duration of antibody positivity and likely time of Leptospira infection using data from a cross-sectional serological study in Fiji. PLoS Negl. Trop. Dis. 16, e0010506 (2022).
- Grillová L et al. Circulating genotypes of Leptospira in French Polynesia: an 9-year molecular epidemiology surveillance follow-up study. PLoS Negl. Trop. Dis. 14, e0008662 (2020).
- Klimpel GR, Matthias MA, Vinetz JM. Leptospira interrogans activation of human peripheral blood mononuclear cells: preferential expansion of TCR gamma delta+ T cells vs TCR alpha beta+ T cells. J. Immunol. 171, 1447–1455 (2003).
- Krangvichian P et al. Impaired functions of human monocyte-derived dendritic cells and induction of regulatory T cells by pathogenic Leptospira. PLoS Negl. Trop. Dis. 17, e0011781 (2023).
- Sumaiya K, Natarajaseenivasan K. Macrophage migration inhibitory factor gene promoter polymorphism (−173G/C SNP) determines host susceptibility and severity of leptospirosis. Microb. Pathog. 164, 105445 (2022).
- Esteves LM et al. Human leptospirosis: seroreactivity and genetic susceptibility in the population of São Miguel Island (Azores, Portugal). PLoS ONE 9, e108534 (2014).
- Fialho RN et al. Role of human leukocyte antigen, killer-cell immunoglobulin-like receptors, and cytokine gene polymorphisms in leptospirosis. Hum. Immunol. 70, 915–920 (2009).
- Charon NW, Greenberg EP, Koopman MB, Limberger RJ. Spirochete chemotaxis, motility, and the structure of the spirochetal periplasmic flagella. Res. Microbiol. 143, 597–603 (1992).
- Vieira DS, Chaurasia R, Vinetz JM. Comparison of the PF07598-encoded virulence-modifying proteins of L. interrogans and L. borgpetersenii. Trop. Med. Infect. Dis. 8, 14 (2023).
- Chaurasia R, Vinetz JM. In silico prediction of molecular mechanisms of toxicity mediated by the leptospiral PF07598 gene family-encoded virulence-modifying proteins. Front. Mol. Biosci. 9, 1092197 (2022).
- Safiee AW et al. Putative pathogenic genes of Leptospira interrogans and Leptospira weilii isolated from patients with acute febrile illness. Trop. Med. Infect. Dis. 7, 284 (2022).
- Pinne M, Choy HA, Haake DA. The OmpL37 surface-exposed protein is expressed by pathogenic leptospira during infection and binds skin and vascular elastin. PLoS Negl. Trop. Dis. 4, e815 (2010).
- Barbosa AS, Isaac L. Strategies used by Leptospira spirochetes to evade the host complement system. FEBS Lett. 594, 2633–2644 (2020).
- Fraga TR, Barbosa AS, Isaac L. Leptospirosis: aspects of innate immunity, immunopathogenesis and immune evasion from the complement system. Scand. J. Immunol. 73, 408–419 (2011).
- Ren SX et al. Unique physiological and pathogenic features of Leptospira interrogans revealed by whole-genome sequencing. Nature 422, 888–893 (2003).
- Carvalho E et al. Leptospiral TlyC is an extracellular matrix-binding protein and does not present hemolysin activity. FEBS Lett. 583, 1381–1385 (2009).
- Segers RP, van Gestel JA, van Eys GJ, van der Zeijst BA, Gaastra W. Presence of putative sphingomyelinase genes among members of the family Leptospiraceae. Infect. Immun. 60, 1707–1710 (1992).
- Narayanavari SA, Sritharan M, Haake DA, Matsunaga J. Multiple leptospiral sphingomyelinases (or are there?). Microbiology 158, 1137–1146 (2012).
- Chacko CS et al. A short review on leptospirosis: clinical manifestations, diagnosis and treatment. Clin. Epidemiol. Glob. Health 11, 100741 (2021).
- Centers for Disease Control and Prevention. Leptospirosis. 2023.
- Ganoza CA et al. Asymptomatic renal colonization of humans in the peruvian Amazon by Leptospira. PLoS Negl. Trop. Dis. 4, e612 (2010).
- Ashford DA et al. Asymptomatic infection and risk factors for leptospirosis in Nicaragua. Am. J. Trop. Med. Hyg. 63, 249–254 (2000).
- Rajapakse S et al. Seroprevalence of leptospirosis in an endemic mixed urban and semi-urban setting — a community-based study in the district of Colombo, Sri Lanka. PLoS Negl. Trop. Dis. 14, e0008309 (2020).
- Almeida DS et al. Investigation of chronic infection by Leptospira spp. in asymptomatic sheep slaughtered in slaughterhouse. PLoS ONE 14, e0217391 (2019).
- Boey K, Shiokawa K, Rajeev S. Leptospira infection in rats: a literature review of global prevalence and distribution. PLoS Negl. Trop. Dis. 13, e0007499 (2019).
- Sant’Anna da Costa R et al. Persistent high leptospiral shedding by asymptomatic dogs in endemic areas triggers a serious public health concern. Animals 2021.
- Ko AI, Goarant C, Picardeau M. Leptospira: the dawn of the molecular genetics era for an emerging zoonotic pathogen. Nat. Rev. Microbiol. 7, 736–747 (2009).
- Rajapakse S. Leptospirosis: clinical aspects. Clin. Med. 22, 14–17 (2022).
- Araujo ER et al. Acute kidney injury in human leptospirosis: an immunohistochemical study with pathophysiological correlation. Virchows Arch. 456, 367–375 (2010).
- Yang CW. Leptospirosis renal disease: understanding the initiation by Toll-like receptors. Kidney Int. 72, 918–925 (2007).
- Rajapakse S et al. Clinical and laboratory associations of severity in a Sri Lankan cohort of patients with serologically confirmed leptospirosis: a prospective study. Trans. R. Soc. Trop. Med. Hyg. 109, 710–716 (2015).
- Nicodemo AC, Duarte-Neto AN. Pathogenesis of pulmonary hemorrhagic syndrome in human leptospirosis. Am. J. Trop. Med. Hyg. 104, 1970–1972 (2021).
- Taylor AJ, Paris DH, Newton PN. A systematic review of the mortality from untreated leptospirosis. PLoS Negl. Trop. Dis. 9, e0003866 (2015).
- Rajapakse S, Rodrigo C, Haniffa R. Developing a clinically relevant classification to predict mortality in severe leptospirosis. J. Emerg. Trauma Shock. 3, 213–219 (2010).
- Bhatia M, Umapathy BL, Navaneeth BV. An evaluation of dark field microscopy, culture and commercial serological kits in the diagnosis of leptospirosis. Indian J. Med. Microbiol. 33, 416–421 (2015).
- Guedes IB et al. Leptospira transport medium (LTM): a practical tool for leptospires isolation. J. Microbiol. Methods 175, 105995 (2020).
- Goarant C, Girault D, Thibeaux R, Soupé-Gilbert ME. Isolation and culture of leptospira from clinical and environmental samples. Methods Mol. Biol. 2134, 1–9 (2020).
- Goris MG, Hartskeerl RA. Leptospirosis serodiagnosis by the microscopic agglutination test. Curr. Protoc. Microbiol. 32, 12E.15 (2014).
- Guernier V, Goarant C, Benschop J, Lau CL. A systematic review of human and animal leptospirosis in the Pacific Islands reveals pathogen and reservoir diversity. PLoS Negl. Trop. Dis. 12, e0006503 (2018).
- Signorini ML, Lottersberger J, Tarabla HD, Vanasco NB. Enzyme-linked immunosorbent assay to diagnose human leptospirosis: a meta-analysis of the published literature. Epidemiol. Infect. 141, 22–32 (2013).
- Rosa MI et al. IgM ELISA for leptospirosis diagnosis: a systematic review and meta-analysis. Cien. Saude Colet. 22, 4001–4012 (2017).
- Sreevalsan TV, Chandra R. Relevance of polymerase chain reaction in early diagnosis of leptospirosis. Indian J. Crit. Care Med. 28, 290–293 (2024).
- Croda J et al. Leptospira immunoglobulin-like proteins as a serodiagnostic marker for acute leptospirosis. J. Clin. Microbiol. 45, 1528–1534 (2007).
- Picardeau M. Diagnosis and epidemiology of leptospirosis. Med. Mal. Infect. 43, 1–9 (2013).
- Levett PN. Usefulness of serologic analysis as a predictor of the infecting serovar in patients with severe leptospirosis. Clin. Infect. Dis. 36, 447–452 (2003).
- Eugene EJ et al. Evaluation of two immunodiagnostic tests for early rapid diagnosis of leptospirosis in Sri Lanka: a preliminary study. BMC Infect. Dis. 15, 319 (2015).
- Goris MG et al. Prospective evaluation of three rapid diagnostic tests for diagnosis of human leptospirosis. PLoS Negl. Trop. Dis. 7, e2290 (2013).
- Behera SK et al. Diagnosis of human leptospirosis: comparison of microscopic agglutination test with recombinant LigA/B antigen-based in-house IgM dot ELISA dipstick test and latex agglutination test using bayesian latent class model and MAT as gold standard. Diagnostics 12, 1455 (2022).
- Suwancharoen D, Sittiwicheanwong B, Wiratsudakul A. Evaluation of loop-mediated isothermal amplification method (LAMP) for pathogenic Leptospira spp. detection with leptospires isolation and real-time PCR. J. Vet. Med. Sci. 78, 1299–1302 (2016).
- Podgoršek D et al. Evaluation of real-time PCR targeting the lipL32 gene for diagnosis of Leptospira infection. BMC Microbiol. 20, 59 (2020).
- Castro-Wallace SL et al. Nanopore DNA sequencing and genome assembly on the international space station. Sci. Rep. 7, 18022 (2017).
- Chiu CY, Miller SA. Clinical metagenomics. Nat. Rev. Genet. 20, 341–355 (2019).
- Allicock OM et al. BacCapSeq: a platform for diagnosis and characterization of bacterial infections. mBio 2018.
- Rajapakse S et al. A diagnostic scoring model for leptospirosis in resource limited settings. PLoS Negl. Trop. Dis. 10, e0004513 (2016).
- Sigera PC et al. Risk prediction for severe disease and better diagnostic accuracy in early dengue infection; the Colombo dengue study. BMC Infect. Dis. 19, 680 (2019).
- Lau CL, DePasquale JM. Leptospirosis, diagnostic challenges, American Samoa. Emerg. Infect. Dis. 18, 2079–2081 (2012).
- De Silva NL et al. Changes in full blood count parameters in leptospirosis: a prospective study. Int. Arch. Med. 7, 31 (2014).
- de Silva NL et al. Can findings on peripheral blood smear differentiate leptospirosis from other infections? A preliminary comparative study. Trans. R. Soc. Trop. Med. Hyg. 112, 94–96 (2018).
- Sukmark T et al. Thai-Lepto-on-admission probability (THAI-LEPTO) score as an early tool for initial diagnosis of leptospirosis: result from Thai-Lepto AKI study group. PLoS Negl. Trop. Dis. 12, e0006319 (2018).
- Temeiam N, Jareinpituk S, Phinyo P, Patumanond J, Srisawat N. Development and validation of a simple score for diagnosis of Leptospirosis at outpatient departments. PLoS Negl. Trop. Dis. 14, e0007977 (2020).
- Al Hariri YK, Sulaiman SAS, Khan AH, Adnan AS, Al Ebrahem SQ. Mortality of leptospirosis associated acute kidney injury (LAKI) & predictors for its development in adults: a systematic review. J. Infect. public. health 12, 751–759 (2019).
- Smith S et al. A simple score to predict severe leptospirosis. PLoS Negl. Trop. Dis. 13, e0007205 (2019).
- Galdino GS et al. Development and validation of a simple machine learning tool to predict mortality in leptospirosis. Sci. Rep. 13, 4506 (2023).
- Marotto PC et al. Early identification of leptospirosis-associated pulmonary hemorrhage syndrome by use of a validated prediction model. J. Infect. 60, 218–223 (2010).
- Pongpan S, Thanatrakolsri P, Vittaporn S, Khamnuan P, Daraswang P. Prognostic factors for leptospirosis infection severity. Trop. Med. Infect. Dis. 2023.
- So RAY et al. A scoring tool to predict pulmonary complications in severe leptospirosis with kidney failure. Trop. Med. Infect. Dis. 2022.
- Ajjimarungsi A, Bhurayanontachai R, Chusri S. Clinical characteristics, outcomes, and predictors of leptospirosis in patients admitted to the medical intensive care unit: a retrospective analysis. J. Infect. Public Health 13, 2055–2061 (2020).
- Guernier V, Allan KJ, Goarant C. Advances and challenges in barcoding pathogenic and environmental Leptospira. Parasitology 145, 595–607 (2018).
- Goarant C. Leptospirosis: risk factors and management challenges in developing countries. Res. Rep. Trop. Med. 7, 49–62 (2016).
- World Health Organization. Human Leptospirosis: Guidance for Diagnosis, Surveillance and Control. 2003.
- Hancock GA, Wilks CR, Kotiw M, Allen JD. The long term efficacy of a hardjo-pomona vaccine in preventing leptospiruria in cattle exposed to natural challenge with Leptospira interrogans serovar hardjo. Aust. Vet. J. 61, 54–56 (1984).
- Rinehart CL, Zimmerman AD, Buterbaugh RE, Jolie RA, Chase CC. Efficacy of vaccination of cattle with the Leptospira interrogans serovar hardjo type hardjoprajitno component of a pentavalent Leptospira bacterin against experimental challenge with Leptospira borgpetersenii serovar hardjo type hardjo-bovis. Am. J. Vet. Res. 73, 735–740 (2012).
- Nisa S et al. Diverse epidemiology of leptospira serovars notified in New Zealand, 1999–2017. Pathogens 2020.
- Win TZ et al. Antibiotic prophylaxis for leptospirosis. Cochrane Database Syst. Rev. 2024.
- Alikhani A et al. Comparison of azithromycin vs doxycycline prophylaxis in leptospirosis, a randomized double blind placebo-controlled trial. J. Infect. Dev. Ctries 12, 991–995 (2018).
- Gonsalez CR et al. Use of doxycycline for leptospirosis after high-risk exposure in São Paulo, Brazil. Rev. Inst. Med. Trop. Sao Paulo 40, 59–61 (1998).
- Illangasekera VL, Kularatne SA, Kumarasiri PV, Pussepitiya D, Premaratne MD. Is oral penicillin an effective chemoprophylaxis against leptospirosis? A placebo controlled field study in the Kandy District, Sri Lanka. Southeast. Asian J. Trop. Med. Public Health 39, 882–884 (2008).
- Sehgal SC, Sugunan AP, Murhekar MV, Sharma S, Vijayachari P. Randomized controlled trial of doxycycline prophylaxis against leptospirosis in an endemic area. Int. J. Antimicrob. Agents 13, 249–255 (2000).
- Takafuji ET et al. An efficacy trial of doxycycline chemoprophylaxis against leptospirosis. N. Engl. J. Med. 310, 497–500 (1984).
- Brett-Major DM, Lipnick RJ. Antibiotic prophylaxis for leptospirosis. Cochrane Database Syst. Rev. 2009.
- Yanagihara Y, Villanueva SY, Yoshida S, Okamoto Y, Masuzawa T. Current status of leptospirosis in Japan and Philippines. Comp. Immunol. Microbiol. Infect. Dis. 30, 399–413 (2007).
- Martínez R et al. Efficacy and safety of a vaccine against human leptospirosis in Cuba. Rev. Panam. Salud Publica 15, 249–255 (2004).
- Laurichesse H et al. Safety and immunogenicity of subcutaneous or intramuscular administration of a monovalent inactivated vaccine against Leptospira interrogans serogroup Icterohaemorrhagiae in healthy volunteers. Clin. Microbiol. Infect. 13, 395–403 (2007).
- Yan Y et al. An evaluation of the serological and epidemiological effects of the outer envelope vaccine to leptospira. J. Chin. Med. Assoc. 66, 224–230 (2003).
- Koizumi N, Watanabe H. Leptospirosis vaccines: past, present, and future. J. Postgrad. Med. 51, 210–214 (2005).
- Wunder EA et al. A live attenuated-vaccine model confers cross-protective immunity against different species of the Leptospira genus. eLife 10, e64166 (2021).
- Silveira MM et al. DNA vaccines against leptospirosis: a literature review. Vaccine 35, 5559–5567 (2017).
- Barazzone GC et al. Revisiting the development of vaccines against pathogenic leptospira: innovative approaches, present challenges, and future perspectives. Front. Immunol. 12, 760291 (2021).
- Lin MH et al. LipL41, a hemin binding protein from Leptospira santarosai serovar Shermani. PLoS ONE 8, e83246 (2013).
- Dellagostin OA et al. Recombinant vaccines against leptospirosis. Hum. Vaccin. 7, 1215–1224 (2011).
- Haake DA et al. Characterization of leptospiral outer membrane lipoprotein LipL36: downregulation associated with late-log-phase growth and mammalian infection. Infect. Immun. 66, 1579–1587 (1998).
- Vijayachari P et al. Immunogenicity of a novel enhanced consensus DNA vaccine encoding the leptospiral protein LipL45. Hum. Vaccin. Immunother. 11, 1945–1953 (2015).
- Buaklin A et al. Optimization of the immunogenicity of a DNA vaccine encoding a bacterial outer membrane lipoprotein. Mol. Biotechnol. 56, 903–910 (2014).
- Faisal SM et al. Evaluation of protective immunity of Leptospira immunoglobulin like protein A (LigA) DNA vaccine against challenge in hamsters. Vaccine 26, 277–287 (2008).
- Feng CY et al. Immune strategies using single-component LipL32 and multi-component recombinant LipL32-41-OmpL1 vaccines against leptospira. Braz. J. Med. Biol. Res. 42, 796–803 (2009).
- Umthong S et al. Immunogenicity of a DNA and recombinant protein vaccine combining LipL32 and Loa22 for leptospirosis using chitosan as a delivery system. J. Microbiol. Biotechnol. 25, 526–536 (2015).
- Kumar P, Lata S, Shankar UN, Akif M. Immunoinformatics-based designing of a multi-epitope chimeric vaccine from multi-domain outer surface antigens of leptospira. Front. Immunol. 2021.
- Validi M, Karkhah A, Prajapati VK, Nouri HR. Immuno-informatics based approaches to design a novel multi epitope-based vaccine for immune response reinforcement against Leptospirosis. Mol. Immunol. 104, 128–138 (2018).
- Techawiwattanaboon T et al. Designing adjuvant formulations to promote immunogenicity and protective efficacy of leptospira immunoglobulin-like protein a subunit vaccine. Front. Cell. Infect. Microbiol. 2022.
- Varma VP, Kadivella M, Kumar A, Kavela S, Faisal SM. LigA formulated in AS04 or montanide ISA720VG induced superior immune response compared to alum, which correlated to protective efficacy in a hamster model of leptospirosis. Front. Immunol. 2022.
- Yang HL et al. In silico and microarray-based genomic approaches to identifying potential vaccine candidates against Leptospira interrogans. BMC Genomics 2006.
- Techawiwattanaboon T et al. Proteomic profile of naturally released extracellular vesicles secreted from leptospira interrogans serovar pomona in response to temperature and osmotic stresses. Sci. Rep. 2023.
- Trott DJ, Abraham S, Adler B. Antimicrobial resistance in Leptospira, Brucella, and other rarely investigated veterinary and zoonotic pathogens. Microbiol. Spectr. 2018.
- Charan J, Saxena D, Mulla S, Yadav P. Antibiotics for the treatment of leptospirosis: systematic review and meta-analysis of controlled trials. Int. J. Prev. Med. 4, 501–510 (2013).
- Suputtamongkol Y et al. An open, randomized, controlled trial of penicillin, doxycycline, and cefotaxime for patients with severe leptospirosis. Clin. Infect. Dis. 39, 1417–1424 (2004).
- Selvarajah S, Ran S, Roberts NW, Nair M. Leptospirosis in pregnancy: a systematic review. PLoS Negl. Trop. Dis. 15, e0009747 (2021).
- Win TZ et al. Antibiotics for treatment of leptospirosis. Cochrane Database Syst. Rev. 2024.
- Fernando N et al. Effect of antimicrobial agents on inflammatory cytokines in acute leptospirosis. Antimicrob. Agents Chemother. 2018.
- Zhang W et al. Doxycycline attenuates leptospira-induced IL-1β by suppressing nlrp3 inflammasome priming. Front. Immunol. 8, 857 (2017).
- Guerrier G, D’Ortenzio E. The Jarisch–Herxheimer reaction in leptospirosis: a systematic review. PLoS ONE 8, e59266 (2013).
- Takamizawa S et al. Leptospirosis and Jarisch–Herxheimer reaction. QJM 108, 967–968 (2015).
- Guerrier G, Lefèvre P, Chouvin C, D’Ortenzio E. Jarisch–Herxheimer reaction among patients with leptospirosis: incidence and risk factors. Am. J. Trop. Med. Hyg. 96, 791–794 (2017).
- Smith S et al. Severe leptospirosis in tropical Australia: optimising intensive care unit management to reduce mortality. PLoS Negl. Trop. Dis. 13, e0007929 (2019).
- Rodrigo C et al. High dose corticosteroids in severe leptospirosis: a systematic review. Trans. R. Soc. Trop. Med. Hyg. 108, 743–750 (2014).
- Davoodi L et al. Evaluation of the effectiveness of N-acetylcysteine on accelerating the recovery of renal failure in patients with leptospirosis, a randomized clinical trial study. Ann. Med. Surg. 67, 102518 (2021).
- Herath N et al. Sequel and therapeutic modalities of leptospirosis associated severe pulmonary haemorrhagic syndrome (SPHS); a Sri Lankan experience. BMC Infect. Dis. 19, 451 (2019).
- Trivedi SV et al. Plasma exchange with immunosuppression in pulmonary alveolar haemorrhage due to leptospirosis. Indian J. Med. Res. 131, 429–433 (2010).
- Fonseka CL, Lekamwasam S. Role of plasmapheresis and extracorporeal membrane oxygenation in the treatment of leptospirosis complicated with pulmonary hemorrhages. J. Trop. Med. 2018, 4520185 (2018).
- Biggs HM et al. Leptospirosis among hospitalized febrile patients in Northern Tanzania. Am. J. Trop. Med. Hyg. 85, 275–281 (2011).
- Ismail TF et al. Retrospective serosurvey of leptospirosis among patients with acute febrile illness and hepatitis in Egypt. Am. J. Trop. Med. Hyg. 75, 1085–1089 (2006).
- Crump JA et al. Etiology of severe non-malaria febrile illness in Northern Tanzania: a prospective cohort study. PLoS Negl. Trop. Dis. 7, e2324 (2013).
- Torgerson PR et al. Global burden of leptospirosis: estimated in terms of disability adjusted life years. PLoS Negl. Trop. Dis. 9, e0004122 (2015).
- Ellis WA. in Leptospira and Leptospirosis. 2015.
- Engida HA, Theuri DM, Gathungu DK, Gachohi J. Optimal control and cost-effectiveness analysis for leptospirosis epidemic. J. Biol. Dyn. 17, 2248178 (2023).
- Sanhueza JM et al. Estimation of the burden of leptospirosis in New Zealand. Zoonoses Public Health 67, 167–176 (2020).
- Galloway RL, Levett PN, Tumeh JW, Flowers CR. Assessing cost effectiveness of empirical and prophylactic therapy for managing leptospirosis outbreaks. Epidemiol. Infect. 137, 1323–1332 (2009).
- Agampodi S, Gunarathna S, Lee JS, Excler JL. Global, regional, and country-level cost of leptospirosis due to loss of productivity in humans. PLoS Negl. Trop. Dis. 17, e0011291 (2023).
- Goris MG et al. Towards the burden of human leptospirosis: duration of acute illness and occurrence of post-leptospirosis symptoms of patients in the Netherlands. PLoS ONE 8, e76549 (2013).
- Cvejic E et al. Contribution of individual psychological and psychosocial factors to symptom severity and time-to-recovery after naturally-occurring acute infective illness: the Dubbo Infection Outcomes Study (DIOS). Brain Behav. Immun. 82, 76–83 (2019).
- Chang CH et al. Long-term outcome of leptospirosis infection with acute kidney injury. Biomedicines 2022.
- Phannajit J et al. Long-term kidney outcomes after leptospirosis: a prospective multicentre cohort study in Thailand. Nephrol. Dial. Transpl. 38, 2182–2191 (2023).
- Premarathne SS et al. Leptospirosis: a potential culprit for chronic kidney disease of uncertain etiology. Nephron 147, 510–520 (2023).
- Carrillo-Larco RM, Altez-Fernandez C, Acevedo-Rodriguez JG, Ortiz-Acha K, Ugarte-Gil C. Leptospirosis as a risk factor for chronic kidney disease: a systematic review of observational studies. PLoS Negl. Trop. Dis. 13, e0007458 (2019).
- Prado LG, Barbosa AS. Understanding the renal fibrotic process in leptospirosis. Int. J. Mol. Sci. 2021.
- Hotez PJ, Aksoy S, Brindley PJ, Kamhawi S. What constitutes a neglected tropical disease?. PLoS Negl. Trop. Dis. 14, e0008001 (2020).
- Hotez PJ, Woc-Colburn L, Bottazzi ME. Neglected tropical diseases in Central America and Panama: review of their prevalence, populations at risk and impact on regional development. Int. J. Parasitol. 44, 597–603 (2014).
- Karpagam KB, Ganesh B. Leptospirosis: a neglected tropical zoonotic infection of public health importance — an updated review. Eur. J. Clin. Microbiol. Infect. Dis. 39, 835–846 (2020).
- Costa E et al. Penicillin at the late stage of leptospirosis: a randomized controlled trial. Rev. Inst. Med. Trop. Sao Paulo 45, 141–145 (2003).
- Daher EF, Nogueira CB. Evaluation of penicillin therapy in patients with leptospirosis and acute renal failure. Rev. Inst. Med. Trop. Sao Paulo 42, 327–332 (2000).
- Edwards CN, Nicholson GD, Hassell TA, Everard CO, Callender J. Penicillin therapy in icteric leptospirosis. Am. J. Trop. Med. Hyg. 39, 388–390 (1988).
- Fairburn AC, Semple SJ. Chloramphenicol and penicillin in the treatment of leptospirosis among British troops in Malaya. Lancet 270, 13–16 (1956).
- McClain JB, Ballou WR, Harrison SM, Steinweg DL. Doxycycline therapy for leptospirosis. Ann. Intern. Med. 100, 696–698 (1984).
- Panaphut T, Domrongkitchaiporn S, Vibhagool A, Thinkamrop B, Susaengrat W. Ceftriaxone compared with sodium penicillin g for treatment of severe leptospirosis. Clin. Infect. Dis. 36, 1507–1513 (2003).
- Phimda K et al. Doxycycline versus azithromycin for treatment of leptospirosis and scrub typhus. Antimicrob. Agents Chemother. 51, 3259–3263 (2007).
- Watt G et al. Placebo-controlled trial of intravenous penicillin for severe and late leptospirosis. Lancet 1, 433–435 (1988).
- Russell RW. Treatment of leptospirosis with oxytetracycline. Lancet 2, 1143–1145 (1958).
- Rajapakse S, Rodrigo C, Balaji K, Fernando SD. Atypical manifestations of leptospirosis. Trans. R. Soc. Trop. Med. Hyg. 109, 294–302 (2015).
- Vilaichone RK, Mahachai V, Wilde H. Acute acalculous cholecystitis in leptospirosis. J. Clin. Gastroenterol. 29, 280–283 (1999).
- Ranawaka N, Jeevagan V, Karunanayake P, Jayasinghe S. Pancreatitis and myocarditis followed by pulmonary hemorrhage, a rare presentation of leptospirosis — a case report and literature survey. BMC Infect. Dis. 13, 38 (2013).
- Solmazgul E et al. A case of Weil’s syndrome developing steroid resistant immune haemolytic anaemia. Scand. J. Infect. Dis. 37, 700–702 (2005).
- Hanvanich M, Moollaor P, Suwangool P, Sitprija V. Hemolytic uremic syndrome in leptospirosis bataviae. Nephron 40, 230–231 (1985).
- Laing RW, Teh C, Toh CH. Thrombotic thrombocytopenic purpura (TTP) complicating leptospirosis: a previously undescribed association. J. Clin. Pathol. 43, 961–962 (1990).
- Panicker JN, Mammachan R, Jayakumar RV. Primary neuroleptospirosis. Postgrad. Med. J. 77, 589–590 (2001).
- Chandra SR et al. Acute disseminated encephalomyelitis following leptospirosis. J. Assoc. Physicians India 52, 327–329 (2004).
- Sakellaridis N, Panagopoulos D, Androulis A. Neuroleptospirosis with hydrocephalus and very elevated cerebrospinal fluid protein. South. Med. J. 102, 549–550 (2009).
- Dimopoulou I et al. Leptospirosis presenting with encephalitis-induced coma. Intensive Care Med. 28, 1682 (2002).
- Kavitha S, Shastry BA. Leptospirosis with transverse myelitis. J. Assoc. Physicians India 53, 159–160 (2005).
- Bal AM, Bharadwaj RS, Gita N, Joshi SA, Thakare JP. Guillain–Barre syndrome in a pediatric patient following infection due to Leptospira. Jpn J. Infect. Dis. 56, 29–31 (2003).
- Hancox RJ, Karalus N, Singh V. Mononeuritis multiplex in leptospirosis. Scand. J. Infect. Dis. 23, 395–396 (1991).
- Turhan V et al. Cerebral venous thrombosis as a complication of leptospirosis. J. Infect. 53, e247–e249 (2006).
- Chu KM, Rathinam R, Namperumalsamy P, Dean D. Identification of Leptospira species in the pathogenesis of uveitis and determination of clinical ocular characteristics in south India. J. Infect. Dis. 177, 1314–1321 (1998).
- Levin N et al. Panuveitis with papillitis in leptospirosis. Am. J. Ophthalmol. 117, 118–119 (1994).
- Faine S, Adler B, Christopher W, Valentine R. Fatal congenital human leptospirosis. Zentralbl. Bakteriol. Mikrobiol. Hyg. A 257, 548 (1984).
- Sharma KK, Madhvilatha P, Kalawat U, Sivakumar V. Leptospirosis-induced still birth and postpartum sepsis. Indian J. Pathol. Microbiol. 54, 426–427 (2011).
- Shaked Y, Shpilberg O, Samra D, Samra Y. Leptospirosis in pregnancy and its effect on the fetus: case report and review. Clin. Infect. Dis. 17, 241–243 (1993).
- Tramoni G, Clément HJ, Lopez F, Viale JP. An unusual case of post partum haemorrhage: leptospirosis infection [French]. Ann. Fr. Anesth. Reanim. 22, 363–365 (2003).
Citations
This article has been cited 11 times.- Ristiyanto R, Handayani FD, Kartika W, Mulyono A, Widoretno W, Maha MS, Lienggonegoro LA, Pangaribuan HU, Suryaningtyas NH, Gasem MH. Application of leptospirosis surveillance study at primary health care center in Banyumas and Demak, Central Java, Indonesia. Open Vet J 2025 Nov;15(11):5961-5970.
- Ruwanpathirana P, Rambukwella R, Perera N, Priyankara D. Severe leptospirosis in the intensive care unit: single centre prospective cohort study from Sri Lanka. BMC Infect Dis 2026 Jan 8;26(1):265.
- Bonilla-Sánchez CA, Rivera-Tenorio A, Álvarez A, Cortés J, Faccini-Martínez ÁA. A case of disseminated intravascular coagulation by leptospirosis during the ongoing yellow fever outbreak in Colombia. New Microbes New Infect 2026 Feb;69:101684.
- Bilung LM, Tahar AS, Pui CF, Bakeri MKS, Su'ut L, Ngui R, Kira R, Apun K. Leptospira and Leptospirosis: A Review of Species Classifications, Genomes, Morphological Structures, Antimicrobial Resistances, Transmissions, and Clinical Manifestations. Curr Microbiol 2026 Jan 5;83(2):122.
- Rosengren P, Johnston L, Ismail I, Smith S, Hanson J. The Characteristics of Patients That Develop Severe Leptospirosis: A Scoping Review. Pathogens 2025 Dec 10;14(12).
- Sykes A, Smith S, Stratton H, Staples M, Rosengren P, Brischetto A, Vincent S, Hanson J. Lung Involvement in Patients with Leptospirosis in Tropical Australia; Associations, Clinical Course and Implications for Management. Trop Med Infect Dis 2025 Nov 26;10(12).
- Kędzierska-Mieszkowska S, Arent Z. Alternative Sigma Factors of RNA Polymerase as Master Regulators in the Pathogenic Spirochaete Leptospira interrogans. Pathogens 2025 Oct 29;14(11).
- Di Azevedo MIN, Lilenbaum W. Genetic Diversity and Clonal Expansion of Pathogenic Leptospira in Brazil: A Multi-Host and Multi-Regional Panorama. Microorganisms 2025 Oct 31;13(11).
- Tan B, De Vera P, Abrazaldo J, Ng C. Flood-associated disease outbreaks and transmission in Southeast Asia. Front Microbiol 2025;16:1694246.
- Timsit JF, Ling L, de Montmollin E, Bracht H, Conway-Morris A, De Bus L, Falcone M, Harris PNA, Machado FR, Paiva JA, Paterson DL, Poulakou G, Roberts JA, Roger C, Shorr AF, Tabah A, Lipman J. Antibiotic therapy for severe bacterial infections. Intensive Care Med 2025 Oct;51(10):1867-1885.
- Stratton H, Rosengren P, Kinneally T, Prideaux L, Smith S, Hanson J. Presentation and Clinical Course of Leptospirosis in a Referral Hospital in Far North Queensland, Tropical Australia. Pathogens 2025 Jun 28;14(7).
Use Nutrition Calculator
Check if your horse's diet meets their nutrition requirements with our easy-to-use tool Check your horse's diet with our easy-to-use tool
Talk to a Nutritionist
Discuss your horse's feeding plan with our experts over a free phone consultation Discuss your horse's diet over a phone consultation
Submit Diet Evaluation
Get a customized feeding plan for your horse formulated by our equine nutritionists Get a custom feeding plan formulated by our nutritionists