- 1One Health Research Group, Universidad de las Américas, Quito, Ecuador
- 2Research Department, SOLCA Núcleo de Quito, Quito, Ecuador
- 3Faculty of Administration and Public Health, Universidad Peruana Cayetano Heredia, San Martín de Porres, Peru
- 4Program in Occupational Safety and Health, The University of Porto, Porto, Portugal
1 Introduction
Scorpions are venomous arthropods belonging to the class Arachnida and the order Scorpiones (1). To date, ~2,772 species of scorpions have been described globally, of which around 104 species (3.8%) are considered of medical significance due to their venom toxicity and potential for severe envenomation (2). The majority of medically relevant species belong to the family Buthidae, which includes genera such as Androctonus, Buthus, Buthotus, Leiurus, Mesobuthus, and Parabuthus, found in regions such as Asia, India, the Middle East, and North Africa. Additionally, species from the Tityus genus are prevalent in South America and the Caribbean, while Centruroides species are commonly encountered in Mexico, Central America, and the southwestern United States (3).
Scorpion envenomation, or scorpionism, is recognized as a pressing yet often neglected public health concern, particularly in tropical and subtropical regions. It disproportionately affects rural and socioeconomically disadvantaged communities, where access to timely and adequate medical care is limited (4, 5). The presence of scorpions in human dwellings and workplaces leads to frequent encounters, thereby elevating the risk of envenomation and associated morbidity and mortality (6–8).
Global estimates suggest that over 1.2 million scorpion stings occur annually, resulting in more than 3,000 deaths, with a disproportionately high burden observed in children due to their lower body mass and increased vulnerability to systemic complications (9–11). Mortality is most prevalent in low-resource settings, where delayed access to antivenom and critical care services remains a major barrier. High-incidence countries include Mexico, Brazil, Iran, Algeria, and Morocco, where scorpionism remains endemic and requires targeted preventive and therapeutic strategies (12–15). Table 1 summarizes the number of reported cases, deaths, and incidence rates per 100,000 inhabitants in selected endemic countries and regions.
2 Biochemical composition and functional diversity of scorpion venom
Scorpion venom is a mixture of lipids, peptides, enzymes, free amino acids, nucleotides, amines, inorganic salts, mucoproteins, heterocyclic components, and various other substances. The composition of the venom can be divided into toxic and non-toxic fractions (3).
The non-toxic fraction includes enzymes such as hyaluronidases, mucopolysaccharides, histamine, and serotonin (3). These components contribute to the overall toxicity of the venom. For instance, hyaluronidase facilitates the spread of toxins by degrading the extracellular matrix and connective tissues surrounding blood vessels at the site of envenomation (3). Histamine plays a role in mediating the inflammatory response (26).
The toxic fraction is mainly composed of neurotoxins, which are capable of depolarizing the membranes of nerve cells through various mechanisms. For example, β-toxins alter the activation of Na+ channels by reducing the peak amplitude of sodium currents and shifting the voltage dependence of channel activation toward more hyperpolarized potentials (27). In contrast, α-toxins inhibit sodium channel deactivation, while κ-neurotoxins block potassium channels (28–30). Meanwhile, calciums act as agonists of ryanodine receptors, increasing intracellular calcium levels (30). Phospholipases disrupt cell membranes by hydrolyzing phospholipids, leading to tissue necrosis and hemorrhage (28, 31). Proteases also play a pivotal role in activating venom toxin precursors through post-translational modifications (3). Proteases are involved in the spread of the toxin through the breakdown of matrix molecules. In addition, proteolytic activity has been observed. Some proteases have been shown to disrupt the transport of pancreatic vesicles to the exterior of the organ, causing pancreatitis (32–34).
Toxins targeting ion channels particularly voltage-gated sodium and potassium channels—are the primary mediators of neurotoxicity and are especially abundant in species such as Mesobuthus tamulus, Hottentotta saulcyi, and Tityus serrulatus (28, 35, 36). These toxins can account for up to 76.7% of venom mass in some species (35). Moreover, scorpion venom includes a wide variety of pharmacologically relevant peptides and proteins, such as antimicrobial, antiviral, antifungal, and antimalarial peptides (37).
Other notable components of scorpion venom include bradykinin-potentiating peptides and cysteine-rich secretory proteins, which contribute to prey immobilization and immune modulation (31, 38). Non-peptidic molecules like adenosine and citric acid are also present and may act synergistically to enhance the envenomation process (39). Lipid components, including phospholipids and ceramides, are involved in cellular disruption and may modulate inflammation (36).
The inflammatory response triggered by scorpion venom involves a cascade of cellular events and mediator release. Upon envenomation, innate immune cells recognize venom components via pattern recognition receptors, leading to the activation of pro-inflammatory signaling pathways (7, 40). This interaction initiates intracellular signaling cascades that result in the release of inflammatory mediators (40).
The cytokine profile induced by scorpion envenomation varies by species. For example, Androctonus australis hector induces the production of IL-1β, IL-4, IL-6, IL-10, and TNF-α; Tityus serrulatus induces IL-1β, IL-6, IL-8, IL-10, NO, TNF-α, IL-1α, IL-1β, IFN-γ, and GM-CSF; Centruroides noxius induces IL-1β, IL-1α, IFN-γ, IL-6, IL-10, and TNF-α. In the case of Leiurus quinquestriatus, the cytokines produced include IL-6, IL-8, NO, and TNF-α (7). These cytokines may be implicated in the pathophysiology of envenomation, such as inflammatory manifestations at the site of inoculation and systemic repercussions, such as pulmonary edema and cardiogenic shock (41, 42).
Despite advances in antivenom therapy, the poor immunogenicity of low molecular mass toxins (3–15 kDa) remains a challenge, as these are often not effectively neutralized by commercial antivenoms (35, 43). Proteomic and transcriptomic studies have revealed a vast diversity in venom composition, which is influenced by species, geographic location, sex, age, and environmental conditions (44). On average, a single scorpion species can produce around 150 different venom components, with ~750 scorpion venom proteins currently cataloged in the UniProt Animal Annotation Program. Toxins are classified based on their ion channel targets: sodium (α-NaScTxs, β-NaScTxs), potassium (α-KTx, β-KTx, γ-KTx, κ-KTx), and calcium (calcines) (27).
Elemental analyses of venom from Androctonus bicolor, Androctonus crassicauda, and Leiurus quinquestriatus have identified the presence of numerous elements, including sodium, potassium, calcium, copper, germanium, cerium, scandium, lanthanum, silver, gallium, palladium, zirconium, neodymium, bismuth, beryllium, tellurium, thallium, samarium, dysprosium, gadolinium, erbium, cesium, holmium, ytterbium, praseodymium, rhenium, europium, arsenic, manganese, chromium, iron, iodine, selenium, lithium, yttrium, nickel, lead, rubidium, rhodium, uranium, antimony, ruthenium, magnesium, phosphorus, silicon, bromine, aluminum, zinc, strontium, vanadium, barium, and titanium (45). This compositional complexity highlights the need for continued research to improve therapeutic approaches and explore the pharmacological potential of scorpion venom components.
3 Risk factors for scorpion stings and severe envenomation
While it is true that one of the main risk factors for scorpion stings is residence in rural areas, where specific environmental and occupational exposures increase the likelihood of encounters. Activities such as storing and handling firewood are particularly hazardous, as they involve prolonged contact with the ground and outdoor environments where scorpions may reside (8). Similarly, the accumulation of leaves, tools, or construction materials near homes provides ideal microhabitats for scorpions, thereby increasing the risk of stings (8).
Notably, some scorpion species exhibit opportunistic behavior, enabling them to adapt to and colonize disturbed or modified environments. These species can establish high-density populations, reproduce rapidly, and survive extended periods without food, allowing them to thrive even under artificial conditions, such as urban settings (14). A prominent example is Tityus serrulatus, whose geographic distribution has expanded significantly across Brazil, with notable proliferation in urban areas (46).
Santana and Oliveira reported that the majority of scorpion envenomation cases occurred in urban and peri-urban areas (65.5%) (47). Another large-scale study in Brazil analyzing 20,555 cases of scorpion stings found that most incidents took place in urban settings (n = 18,571; 90.35%) (48). Similarly, Furtado et al. (49) observed a high frequency of urban cases (n = 9,625; 86.45%) in the state of Ceará, Brazil.
Another relevant risk factor is the presence of birds in the household environment. The straw used in nests serves as a suitable shelter for scorpions, facilitating their proximity to humans (8, 50). Housing conditions also play a critical role. Dwellings constructed with non-durable materials such as tin, wood, or cardboard roofs and dirt floors are more permeable to scorpion intrusion. Additionally, inadequate structural integrity and proximity to natural scorpion habitats further increase the risk of indoor colonization (5, 50). In rural contexts, children frequently assist in agricultural tasks, which further elevate their exposure and risk of stings (50).
Beyond structural and behavioral determinants, several demographic and environmental factors contribute to the epidemiology of scorpionism. Age is a critical determinant of severity, with children particularly those under 15 years being more susceptible to severe envenomation and fatal outcomes (51–53). Occupational exposure remains a significant risk factor, notably among farmers, homemakers, and individuals who handle firewood or rear domestic animals such as ducks and hens (8, 50).
Temporal patterns also modulate risk: stings are more frequent during warmer seasons and nocturnal hours, coinciding with increased scorpion activity (52). Delays in seeking medical care particularly those exceeding 3 h and the inadequate use of antivenom are associated with increased mortality, especially among pediatric populations (51). Emerging evidence has further suggested a possible link between scorpion envenomation and long-term cardiovascular complications, including the development of dilated cardiomyopathy (54).
Inappropriate use of antivenoms remains a critical concern. Fatal outcomes have been associated with improper antivenom administration (51). A study conducted in Brazil involving 293 envenomation cases found that antivenom was inappropriately prescribed in the majority of treated patients (59.7%). Among these cases, the most frequent error was the administration of a higher number of vials than recommended (124 cases; 72.1%), resulting in a total of 323 vials administered beyond protocol guidelines (47). This misuse may stem from the absence of up-to-date reference materials, ineffective dissemination of treatment protocols, and a lack of regular training in the diagnosis and management of scorpion envenomation (47). However, with proper use of antivenom and timely administration, clinical conditions usually improve rapidly, and plasma venom levels generally become undetectable within an hour of starting treatment. Additionally, antivenom reduces the mortality rate even in cases of severe envenomation. It has also been observed that in critically ill children with neurotoxic effects from scorpion envenomation, intravenous administration of scorpion-specific antivenom resolved the clinical syndrome within 4 h (30, 55, 56).
4 Public health intervention
4.1 Challenges and imperatives in antiserum production
The production and equitable distribution of therapeutic antisera represent a critical, yet often overlooked, component of public health systems particularly in low- and middle-income countries. Despite the availability of technical guidelines and protocols for the manufacture of animal-derived antisera, such as whole IgG or F(ab')2 fragments, many public-sector laboratories operate under severe constraints. These include limited production capacity, outdated infrastructure, and insufficient regulatory oversight, all of which hinder their ability to ensure the safety, efficacy, and sustainability of antiserum supply (57, 58).
In Ecuador, the cessation of local snake antivenom production illustrates the vulnerability caused by the absence of long-term planning in serum policy. Historically self-sufficient, the country's sole antivenom manufacturing facility was closed in 2012 amid structural reforms and administrative decentralization, without establishing a sustainable alternative (59). Since then, Ecuador has become entirely dependent on imports for instance, acquiring 42,883 vials from Costa Rica between 2015 and 2017 while facing an increase in snakebite-related hospitalizations and case severity, particularly in remote Amazonian and coastal regions with limited access to emergency care (59).
Another critical issue is the improper storage and transportation of antisera, which can lead to the deterioration or destruction of vials and ampoules. A notable example is the absence of a reliable cold chain, which is essential for preserving the efficacy of liquid antisera. Without appropriate refrigeration, these biological products may become ineffective and unusable (58).
To address global deficiencies in antivenom supply, the World Health Organization (2007) proposed a comprehensive strategy that includes (Table 2):
• Investment in infrastructure and staff training
• Implementation of Good Manufacturing Practices (GMP)
• Strengthening regulatory systems
• Establishment of prequalification programs
• Improved distribution networks guided by epidemiological data
• Continuous clinical training to ensure rational antiserum use

Table 2. WHO strategic actions for strengthening antiserum production and distribution systems in public health.
One of the most persistent barriers is the lack of coordination between epidemiological surveillance teams and antivenom distribution planners. This misalignment often leads to overstocking in urban hospitals, while rural health posts where most envenomations occur remain under-resourced. Additionally, frontline health workers in these underserved areas frequently lack adequate training in antivenom administration, further exacerbating preventable morbidity and mortality (57, 58).
Ecuador's experience highlights the pressing need to re-establish regional antivenom production capabilities, not only to improve response times but also to enhance health system resilience amid rising envenomation rates. A coordinated regional approach driven by WHO, national governments, and local stakeholders is essential to restore serum availability and reduce the public health burden associated with venomous animal encounters.
Further research is critically needed to evaluate the neutralization efficacy of existing antivenoms against all venomous species endemic to each country. Antivenoms tend to be highly specific to the venom of the species from which they are derived, and cross-neutralization with venom from other species is often limited (60). While in some instances cross-reactivity does occur—as in the case of A. crassicauda antivenom (RSHC anti-Ac), which demonstrates immunoreactivity and neutralization potential against Leiurus quinquestriatus (61), this is not universally applicable. For example, scorpions of the Tityus genus exhibit a high antigenic diversity in their venom, and despite the taxonomic diversity of Tityus, only three anti-Tityus antivenoms are available in the Americas, targeting T. serrulatus, T. trivittatus, and T. discrepans (62).
It has been demonstrated that antivenoms often show reduced efficacy outside the native distribution area of the scorpion species for which they were developed. For instance, the Venezuelan anti-T. discrepans antivenom does not effectively neutralize the venom of T. pachyurus from Colombia, and the Brazilian anti-T. serrulatus antivenom is not capable of significantly reversing the severity of cerebellar-muscular symptoms caused by T. obscurus (62). The lack of species-specific antivenoms represents a serious public health concern. In Iraq, for example, fatalities occasionally occur due to the unavailability of antivenoms specific to local scorpion species (60).
4.2 Role of national authorities in scorpionism prevention and control
4.2.1 Ministry of public health
As the principal agency responsible for protecting population health, the Ministry of Public Health plays a pivotal role in mitigating the public health burden of scorpion envenomation. A fundamental responsibility is ensuring that healthcare professionals particularly those deployed to rural or high-risk areas receive comprehensive training in the clinical recognition and management of scorpion stings prior to assignment (2). This clinical preparedness should be complemented by national public awareness campaigns designed to educate communities on preventive practices, the early signs of envenomation, and the importance of timely medical intervention. These initiatives must be accompanied by robust monitoring and evaluation mechanisms to assess outreach effectiveness and inform policy refinement (2).
At the community level, targeted interventions such as educational workshops can empower local populations to identify medically relevant scorpion species and implement basic environmental control measures. These may include clearing debris, removing weeds, sealing structural gaps, and maintaining household hygiene to minimize scorpion habitats (9, 63). Such community engagement is essential for promoting sustained behavioral change and environmental risk reduction.
Equally critical is the strengthening of epidemiological surveillance systems. Enhanced reporting mechanisms potentially facilitated through mobile health technologies can improve the timeliness and accuracy of sting notifications. Collaborations with local health authorities, civil society, and academic institutions can support the continuous mapping of scorpion species distribution and identify emerging envenomation hotspots (5).
Furthermore, the establishment of national research centers focused on scorpionism would provide the scientific foundation for long-term mitigation strategies. These centers should prioritize interdisciplinary research on venom composition, species ecology, and vector control techniques, thereby facilitating the development of regionally tailored antivenoms and evidence-based interventions (2).
4.2.2 Ministry of public education
Long-term prevention of scorpion stings requires the active involvement of the Ministry of Education through the integration of relevant content into national curricula. Educational programs should include topics on medically important arthropods particularly scorpions to raise awareness among children about envenomation risks, prevention strategies, and the identification of venomous species (2). Instilling these concepts from an early age can reduce the incidence of stings at home and foster a community-wide culture of prevention. It is also important to educate about the importance of ensuring that household waste is properly sealed in plastic bags or other tightly closed containers and is disposed of on the correct day for collection services (64).
Such content should be embedded within science and health education modules and supported by age-appropriate educational materials, including posters, illustrated guides, and digital platforms. To ensure accuracy and engagement, teachers must be adequately trained to deliver evidence-based information tailored to local epidemiological contexts.
Complementary initiatives such as science clubs, school fairs, and interactive workshops can reinforce key prevention messages, especially in endemic regions. By empowering children as health promoters, early education serves not only to protect individual students but also to disseminate knowledge within families and across generations, thereby enhancing community resilience (2).
4.2.3 Ministry of agriculture and environment
The Ministry of Agriculture and Environment holds a pivotal role in reducing scorpion sting incidence through both occupational safety measures and environmental risk mitigation. Agricultural and livestock workers are among the most exposed populations; therefore, the promotion of personal protective equipment such as boots and gloves is essential for minimizing contact with scorpions in high-risk settings (2, 65).
Public awareness campaigns should also address harmful practices such as illegal burning of vegetation, which can disrupt scorpion habitats and inadvertently increase human-scorpion interactions. In parallel, the Ministry should advocate for the safe storage of firewood, crop residues, and construction materials to limit the formation of suitable refuges for scorpions.
To ensure sustained impact, intersectoral collaboration with local governments, academic institutions, and public health authorities is necessary. Joint efforts to map high-risk zones, implement ecological pest control strategies, and integrate environmental sustainability into prevention policies can strengthen the country's capacity to address scorpionism as both a health and environmental challenge (2).
5 Conclusion
Scorpionism remains a neglected yet impactful public health issue, disproportionately affecting vulnerable populations in tropical and subtropical regions. Despite its significant global burden, it continues to be overlooked by health authorities and excluded from major international health agendas. Given its epidemiological, social, and economic consequences, scorpionism warrants formal recognition as a neglected tropical disease.
The multifactorial nature of scorpion envenomation shaped by ecological conditions, population vulnerability, health system limitations, and socioeconomic inequalities—demands a coordinated, multisectoral response that integrates environmental management, health education, clinical preparedness, and local antivenom production.
National authorities particularly the ministries of health, education, agriculture, and environment must coordinate efforts to address structural risk factors such as unsafe housing, occupational exposure, and limited access to timely care in rural areas. This includes strengthening regional capacity for antivenom production, improving clinical training in envenomation management, and embedding prevention strategies into school curricula and community programs to foster long-term risk reduction and a culture of awareness and resilience.
Author contributions
JV-G: Writing – review & editing, Writing – original draft. HA-L: Writing – review & editing, Writing – original draft. MN-L: Writing – review & editing, Writing – original draft. JI-C: Writing – review & editing. EP-V: Writing – review & editing. EO-P: Writing – original draft, Writing – review & editing.
Funding
The author(s) declare that no financial support was received for the research and/or publication of this article.
Conflict of interest
The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.
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The author(s) declare that Gen AI was used in the creation of this manuscript. Generative AI was used in the preparation of this manuscript for spelling and grammar correction, and for improving syntax and clarity of language. It was not used for content generation or data analysis.
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References
1. Cloudsley-Thompson JL. Spiders and scorpions (Araneae and Scorpiones). In:Lane RP, Crosskey RW, , editors. Medical Insects and Arachnids. Dordrecht: Springer Netherlands (1993). p. 659–82.
2. Hernández-Muñoz EA, Zavala-Sánchez EV, Rubio-Atondo A, López-Chávez JA, Arredondo-Rojas V, Reyes-Reyes JS. Scorpion sting envenomation outbreak in Mexico. Strat. Prevent. Control Toxicon. (2024) 237:107549. doi: 10.1016/j.toxicon.2023.107549
3. Mabunda IG, Zinyemba NK, Pillay S, Offor BC, Muller B, Piater LA. The geographical distribution of scorpions, implication of venom toxins, envenomation, and potential therapeutics in Southern and Northern Africa. Toxicol Res. (2024) 13:tfae118. doi: 10.1093/toxres/tfae118
4. Kumar A, Goyal S, Garg MK, Gopalakrishnan M. Scorpion sting envenomation, a neglected tropical disease: a nationwide survey exploring perspectives and attitudes of resident doctors from India. Am J Trop Med Hyg. (2023) 109:957–64. doi: 10.4269/ajtmh.23-0194
5. Vasconez-Gonzalez J, Izquierdo-Condoy JS, Miño C, de Lourdes Noboa-Lasso M, Ortiz-Prado E. Epidemiological and geodemographic patterns of scorpionism in ecuador: a nationwide analysis (2021–2024). Toxicon X. (2025) 18:100218. doi: 10.1016/j.toxcx.2025.100218
6. Barros RM, Pasquino JA, Peixoto LR, Targino ITG, Sousa JA de, Leite R de S. Clinical and epidemiological aspects of scorpion stings in the northeast region of Brazil. Ciênc Saúde Coletiva. (2014) 19:1275–82. doi: 10.1590/1413-81232014194.01602013
7. Petricevich VL. Scorpion venom and the inflammatory response. Mediators Inflamm. (2010) 2010:903295. doi: 10.1155/2010/903295
8. Trinidad-Porfirio BE, Morales-Pérez A, Nava-Aguilera E, Flores-Moreno M, Morales-Nava L, García-Leyva J, et al. Occurrence of scorpion sting and associated factors in a highly marginalized municipality in Guerrero, Mexico: a cross-sectional study. PLoS Negl Trop Dis. (2023) 17:e0011271. doi: 10.1371/journal.pntd.0011271
9. Chippaux JP, Goyffon M. Epidemiology of scorpionism: a global appraisal. Acta Trop. (2008) 107:71–9. doi: 10.1016/j.actatropica.2008.05.021
11. Choppari K, Soma SK, Thomas SR. Socio-demographic, clinical, laboratory profile and outcome in children with scorpion envenomation. Int J Contemp Pediatr. (2021) 8:268–72. doi: 10.18203/2349-3291.ijcp20210111
12. Bourée P, Frinot Joseph P, Fernot Joseph P, Gil REM, Fils-Aimé F, Barrera RR, et al. [Scorpion stings: a public health problem in Morelos (Mexico)]. Sante Montrouge Fr. (2005) 15:217–23.
13. El Oufir R, Semlali I, Idrissi M, Soulaymani A, Benlarabi S, Khattabi A, et al. Scorpion sting: a public health problem in El Kelaa des Sraghna (Morocco). J Venom Anim Toxins Trop Dis. (2008) 14:258–73. doi: 10.1590/S1678-91992008000200005
14. Guerra-Duarte C, Saavedra-Langer R, Matavel A, Oliveira-Mendes BBR, Chavez-Olortegui C, Paiva ALB. Scorpion envenomation in Brazil: current scenario and perspectives for containing an increasing health problem. PLoS Negl Trop Dis. (2023) 17:e0011069. doi: 10.1371/journal.pntd.0011069
15. Laïd Y, Boutekdjiret L, Oudjehane R, Laraba-Djebari F, Hellal H, Guerinik M, et al. Incidence and severity of scorpion stings in Algeria. J Venom Anim Toxins Trop Dis. (2012) 18:399–410. doi: 10.1590/S1678-91992012000400008
16. Lacerda AB, Lorenz C, De Azevedo TS, Cândido DM, Wen FH, Eloy LJ, et al. Scorpion envenomation in the state of São Paulo, Brazil: spatiotemporal analysis of a growing public health concern. PLoS ONE. (2022) 17:e0266138. doi: 10.1371/journal.pone.0266138
17. Ministério da Saúde. Governo Federal. Boletim Epidemiológico - Volume 55 - no 06 — Ministério da Saúde (2024). Available online at: https://www.gov.br/saude/pt-br/centrais-de-conteudo/publicacoes/boletins/epidemiologicos/edicoes/2024/boletim-epidemiologico-volume-55-no-06/view (accessed March 31, 2025).
18. Ministère de la Santé. INSP. Ministère de la Santé Institut National de Santé Publique (2023). Available online at: http://www.insp.dz/index.php/Non-categorise/rem.html (accessed March 31, 2025).
19. Dehghani R, Fathi B. Scorpion sting in Iran: a review. Toxicon. (2012) 60:919–33. doi: 10.1016/j.toxicon.2012.06.002
20. Mahshidfar B, Basir Ghafouri H, Yasinzadeh MR, Mofidi M, Rezai M, Farsi D, et al. Demographics of scorpion sting in Iran; a cross sectional study. Emergency. (2017) 5:e77. doi: 10.22037/emergency.v5i1.18276
21. Chakroun-Walha O, Karray R, Jerbi M, Nasri A, Issaoui F, Amine BR, et al. Update on the epidemiology of scorpion envenomation in the south of Tunisia. Wilderness Environ Med. (2018) 29:29–35. doi: 10.1016/j.wem.2017.09.011
22. Centre antipoison et de pharmacovigilance du Maroc. TOXICOVIGILANCE RAPPORTS GENERAL ET SPECIFIQUES ANNEE 2019 (2019). Available online at: https://www.capm-sante.ma/uploads/documents/81.pdf (accessed March 31, 2025).
23. Elmourid A, Elhidan MA, Boussaa S, Bhiri M, Touloun O. Epidemiological and faunistic characterization of scorpionism in the Beni Mellal-Khenifra region, Central Morocco. Toxicon. (2022) 218:70–5. doi: 10.1016/j.toxicon.2022.09.001
24. Alhamoud MA, Al Fehaid MS, Alhamoud MA, Alzoayed MH, Alkhalifah AA, Menezes RG. Scorpion stings in Saudi Arabia: an overview. Acta Bio Medica Atenei Parm. (2021) 92:e2021273.
25. Ozkan O, Uzun R, Adigüzel S, Cesaretli Y, Ertek M. Evaluation of scorpion sting incidence in Turkey. J Venom Anim Toxins Trop Dis. (2008) 14. doi: 10.1590/S1678-91992008000100010
26. Adi-Bessalem S, Hammoudi-Triki D, Laraba-Djebari F. Scorpion Venom Interactions with the Immune System. In:Gopalakrishnakone P, , editor. Toxinology: Scorpion Venoms. Dordrecht: Netherlands: Springer (2021). p. 1–18.
27. Quintero-Hernández V, Jiménez-Vargas JM, Gurrola GB, Valdivia HHF, Possani LD. Scorpion venom components that affect ion-channels function. Toxicon Off J Int Soc Toxinology. (2013) 76:328–42. doi: 10.1016/j.toxicon.2013.07.012
28. Ahmadi S, Knerr JM, Argemi L, Bordon KCF, Pucca MB, Cerni FA, et al. Scorpion venom: detriments and benefits. Biomedicines. (2020) 8:118. doi: 10.3390/biomedicines8050118
29. Del Brutto OH. Neurological effects of venomous bites and stings: snakes, spiders, and scorpions. Handb Clin Neurol. (2013) 114:349–68. doi: 10.1016/B978-0-444-53490-3.00028-5
30. Vasconez-Gonzalez J, Delgado-Moreira K, Gamez-Rivera E, Lopez-Molina MB, Davila FL, Izquierdo-Condoy JS, et al. Stroke as a rare complication of scorpion stings: A systematic review and analysis. Toxicon X. (2024) 24:100205. doi: 10.1016/j.toxcx.2024.100205
31. Tobassum S, Tahir HM, Arshad M, Zahid MT, Ali S, Ahsan MM. Nature and applications of scorpion venom: an overview. Toxin Rev. (2020) 39:214–25. doi: 10.1080/15569543.2018.1530681
32. Carmo AO, Oliveira-Mendes BBR, Horta CCR, Magalhães BF, Dantas AE, Chaves LM, et al. Molecular and functional characterization of metalloserrulases, new metalloproteases from the Tityus serrulatus venom gland. Toxicon. (2014) 90:45–55. doi: 10.1016/j.toxicon.2014.07.014
33. Fletcher PL, Fletcher MD, Weninger K, Anderson TE, Martin BM. Vesicle-associated Membrane Protein (VAMP) Cleavage by a new metalloprotease from the Brazilian scorpion tityus serrulatus. J Biol Chem. (2010) 285:7405–16. doi: 10.1074/jbc.M109.028365
34. Gunas V, Maievskyi O, Raksha N, Vovk T, Savchuk O, Shchypanskyi S, et al. The activity of metalloproteases and serine proteases in various organs after leiurus macroctenus envenomation. J Toxicol. (2023) 2023:5262729. doi: 10.1155/2023/5262729
35. Das B, Patra A, Mukherjee AK. Correlation of venom toxinome composition of Indian red scorpion (Mesobuthus tamulus) with clinical manifestations of scorpion stings: failure of commercial antivenom to immune-recognize the abundance of low molecular mass toxins of this venom. J Proteome Res. (2020) 19:1847–56. doi: 10.1021/acs.jproteome.0c00120
36. Ghezellou P, Jakob K, Atashi J, Ghassempour A, Spengler B. Mass-Spectrometry-based lipidome and proteome profiling of Hottentotta saulcyi (Scorpiones: Buthidae) Venom. Toxins. (2022) 14:370. doi: 10.3390/toxins14060370
37. Ortiz E, Gurrola GB, Schwartz EF, Possani LD. Scorpion venom components as potential candidates for drug development. Toxicon. (2015) 93:125–35. doi: 10.1016/j.toxicon.2014.11.233
38. De Oliveira UC, Nishiyama MY Jr, Dos Santos MBV, de Santos-da-Silva A, de Menezes Chalkidis H, Souza-Imberg A, et al. Proteomic endorsed transcriptomic profiles of venom glands from Tityus obscurus and T serrulatus scorpions. PLoS ONE. (2018) 13:e0193739. doi: 10.1371/journal.pone.0193739
39. Evans ERJ, McIntyre L, Northfield TD, Daly NL, Wilson DT. Small molecules in the venom of the scorpion Hormurus waigiensis. Biomedicines. (2020) 8:259. doi: 10.3390/biomedicines8080259
40. Reis MB, Zoccal KF, Gardinassi LG, Faccioli LH. Scorpion envenomation and inflammation: beyond neurotoxic effects. Toxicon. (2019) 167:174–9. doi: 10.1016/j.toxicon.2019.06.219
41. Reis MB, Rodrigues FL, Lautherbach N, Kanashiro A, Sorgi CA, Meirelles AFG, et al. Interleukin-1 receptor-induced PGE2 production controls acetylcholine-mediated cardiac dysfunction and mortality during scorpion envenomation. Nat Commun. (2020) 11:5433. doi: 10.1038/s41467-020-19232-8
42. Zoccal KF, Sorgi CA, Hori JI, Paula-Silva FWG, Arantes EC, Serezani CH, et al. Opposing roles of LTB4 and PGE2 in regulating the inflammasome-dependent scorpion venom-induced mortality. Nat Commun. (2016) 7:10760. doi: 10.1038/ncomms10760
43. Cid-Uribe JI, Veytia-Bucheli JI, Romero-Gutierrez T, Ortiz E, Possani LD. Scorpion venomics: a 2019 overview. Expert Rev Proteomics. (2020) 17:67–83. doi: 10.1080/14789450.2020.1705158
44. Romero-Gutiérrez MT, Santibáñez-López CE, Jiménez-Vargas JM, Batista CVF, Ortiz E, Possani LD. Transcriptomic and proteomic analyses reveal the diversity of venom components from the Vaejovid scorpion Serradigitus gertschi. Toxins. (2018) 10:359. doi: 10.3390/toxins10090359
45. Al-Asmari AK, Kunnathodi F, Al Saadon K, Idris MM. Elemental analysis of scorpion venoms. J Venom Res. (2016) 7:16–20.
46. Lourenço WR. What do we know about some of the most conspicuous scorpion species of the genus Tityus? A historical approach. J Venom Anim Toxins Trop Dis. (2015) 21:20. doi: 10.1186/s40409-015-0016-9
47. Santana CR, Oliveira MG. Evaluation of the use of antivenom sera in the emergency service of a regional public hospital in Vitória da Conquista (BA), Brazil. Ciênc Saúde Colet. (2020) 25:869–78. doi: 10.1590/1413-81232020253.16362018
48. de Araújo KAM, Tavares AV, Marques MR de V, Vieira AA, Leite R de S. Epidemiological study of scorpion stings in the Rio Grande do Norte State, Northeastern Brazil. Rev Inst Med Trop São Paulo. (2017) 59:e58. doi: 10.1590/s1678-9946201759058
49. Furtado S da S, Belmino JFB, Diniz AGQ, Leite Rde S. EPIDEMIOLOGY OF SCORPION ENVENOMATION IN THE STATE OF CEARÁ, NORTHEASTERN BRAZIL. Rev Inst Med Trop São Paulo. (2016) 58:15. doi: 10.1590/S1678-9946201658015
50. Silva-Domínguez R, Paredes-Solís S, Cortés-Guzmán AJ, Flores-Moreno M, Baldazo-Monsivaiz JG, Anderson N, et al. Factores asociados con la picadura de alacrán en escolares: estudio transversal en dos comunidades rurales de Guerrero, México. Bol Méd Hosp Infant México. (2019) 76:79–86. doi: 10.24875/BMHIM.18000104
51. Almeida ACC, Carvalho FM, Mise YF. Risk factors for fatal scorpion envenoming among Brazilian children: a case-control study. Trans R Soc Trop Med Hyg. (2021) 115:975–83. doi: 10.1093/trstmh/trab120
52. Hmimou R, Soulaymani A, Mokhtari A, Arfaoui A, Eloufir G, Semlali I, et al. Risk factors caused by scorpion stings and envenomations in the province of Kelâa Des Sraghna (Morocco). J Venom Anim Toxins Trop Dis. (2008) 14:628–40. doi: 10.1590/S1678-91992008000400006
53. Takehara CA, Lamas JLT, Gasparino RC, Fusco SFB. Moderate or severe scorpion sting: identification of risk factors. Rev Esc Enferm U.P. (2023) 57:e20230022. doi: 10.1590/1980-220x-reeusp-2023-0022pt
54. Sundararaman T, Olithselvan M, Sethuraman KR, Narayan KA. Scorpion envenomation as a risk factor for development of dilated cardiomyopathy. J Assoc Physicians India. (1999) 47:1047–50.
55. Boyer LV, Theodorou AA, Berg RA, Mallie J, Chávez-Méndez A, García-Ubbelohde W, et al. Antivenom for critically Ill children with neurotoxicity from Scorpion stings. N Engl J Med. (2009) 360:2090–8. doi: 10.1056/NEJMoa0808455
56. Çigdem El, Çelikkaya ME. Administration of a second dose antivenom in the early period: is it effective in scorpion stings? J Pediat Res. (2020) 7:126–31. doi: 10.4274/jpr.galenos.2019.45087
57. World Health Organization. Snakebite envenoming (2023). Available online at: https://www.who.int/news-room/fact-sheets/detail/snakebite-envenoming (accessed March 31, 2025).
58. WHO. Rabies and envenomings : a neglected public health issue : report of a consultative meeting (2007). Available online at: https://iris.who.int/bitstream/handle/10665/43858/9789241563482_eng.pdf (accessed March 31, 2025).
59. Ortiz-Prado E, Yeager J, Andrade F, Schiavi-Guzman C, Abedrabbo-Figueroa P, Terán E, et al. Snake antivenom production in Ecuador: Poor implementation, and an unplanned cessation leads to a call for a renaissance. Toxicon Off J Int Soc Toxinol. (2021) 202:90–7. doi: 10.1016/j.toxicon.2021.09.014
60. Ismael BN, Abass KS, Khalil KA, Salih KA. Preparation of F(ab')2 antivenom in Iraq against scorpion (Hottentotta saulcyi) venom. Biologicals. (2018) 56:19–23. doi: 10.1016/j.biologicals.2018.08.005
61. Ozkan O, Adiguzel S, Inceoglu B, Lango J, Ertek M, Hammock BD. Evaluation of the neutralizing capacity of Androctonus crassicauda (Olivier, 1807) antivenom against Leiurus quinquestriatus (Ehrenberg, 1928) venom (Scorpiones: Buthidae). J Venom Anim Toxins Trop Dis. (2008) 14:481–96. doi: 10.1590/S1678-91992008000300008
62. Borges A, Lomonte B, Angulo Y, Acosta de. Patiño H, Pascale JM, Otero R, et al. Venom diversity in the neotropical scorpion genus Tityus: implications for antivenom design emerging from molecular and immunochemical analyses across endemic areas of scorpionism. Acta Trop. (2020) 204:105346. doi: 10.1016/j.actatropica.2020.105346
63. Queiroz AM, Sampaio VS, Mendonça I, Fé NF, Sachett J, Ferreira LCL, et al. Severity of Scorpion stings in the Western Brazilian Amazon: a case-control study. PLoS ONE. (2015) 10:e0128819. doi: 10.1371/journal.pone.0128819
64. Guerra RO, Gonçalves D de A, Moretti B, Bresciani KDS. Prevention, surveillance, and scorpion accident control: an integrative review. Res Soc Dev. (2022) 11:e22111032302. doi: 10.33448/rsd-v11i10.32302
Keywords: scorpionism, scorpion stings, neglected tropical disease, public health, global health
Citation: Vasconez-Gonzalez J, Alexander-León H, Noboa-Lasso MdL, Izquierdo-Condoy JS, Puente-Villamarín E and Ortiz-Prado E (2025) Scorpionism: a neglected tropical disease with global public health implications. Front. Public Health 13:1603857. doi: 10.3389/fpubh.2025.1603857
Received: 01 April 2025; Accepted: 23 April 2025;
Published: 03 June 2025.
Edited by:
Clara Guerra-Duarte, Ezequiel Dias Foundation (FUNED), BrazilReviewed by:
Mouzarllem Barros Reis, University of São Paulo, BrazilAna Luiza Paiva, Ezequiel Dias Foundation (FUNED), Brazil
Copyright © 2025 Vasconez-Gonzalez, Alexander-León, Noboa-Lasso, Izquierdo-Condoy, Puente-Villamarín and Ortiz-Prado. This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
*Correspondence: Esteban Ortiz-Prado, ZS5vcnRpenByYWRvQGdtYWlsLmNvbQ==