Medicine:Pathophysiology of spider bites

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Short description: Reactions to venom of spider bites

The pathophysiology of a spider bite is due to the effect of its venom. A spider envenomation occurs whenever a spider injects venom into the skin. Not all spider bites inject venom – a dry bite, and the amount of venom injected can vary based on the type of spider and the circumstances of the encounter. The mechanical injury from a spider bite is not a serious concern for humans. Some spider bites do leave a large enough wound that infection may be a concern. However, it is generally the toxicity of spider venom that poses the most risk to human beings; several spiders are known to have venom that can cause injury to humans in the amounts that a spider will typically inject when biting.

Only a small percentage of species have bites that pose a danger to people. Many spiders do not have mouthparts capable of penetrating human skin. While venoms are by definition toxic substances, most spiders do not have venom that is toxic to humans (in the quantities delivered) to require medical attention. Of those that do, fatal outcomes are exceedingly rare.[citation needed]

Spider venoms work on one of two fundamental principles; they are either neurotoxic (impairing the nervous system) or necrotic (dissolving tissues surrounding the bite). In some cases, the venom targets vital organs and systems.

Neurotoxic venom

Spiders paralyze prey with neurotoxic venom of some sort. A few have a venom that cross reacts with mammalian nervous system, though the specific manner in which the nervous system is attacked varies from spider to spider.[1][2][3] When motor neurons are excited the symptoms include muscle spasms, cramps, and twitching. When autonomic nerves are involved sweating, drooling, gooseflesh. In the extreme unstable blood pressure and heart rate can result.[citation needed]

  • Widow spider venom contains components known as latrotoxins, which cause the massive release of the neurotransmitters causing muscle contractions, sweating, and gooseflesh. This can affect the body in several ways, including causing painful abdominal cramps[4]
  • The atracotoxins of Australian funnel-web spiders work by opening sodium channels, causing excessive neural activity including strange sensations (paresthesias), muscle contractions, unstable blood pressure (hypertension or hypotension). The venom may cause fluid to accumulate in the lungs (pulmonary edema) that can be fatal.
  • The venom of Brazilian wandering spiders is also a potent neurotoxin, which attacks multiple types of ion channels.[5] Principally generating severe pain that travels up the limb, autonomic effects, including painful erections, occur with moderate envenomation. With severe envenomation heart and lung failure can result in death. In addition, the venom contains high levels of serotonin, making an envenomation by this species particularly painful.

Necrotic venom

Spiders known to have necrotic venom occur most notoriously in the family Sicariidae, which includes both the recluse spiders and the six-eyed sand spiders in the genus Hexophthalma and Sicarius. Spiders in this family possess a known dermonecrotic agent sphingomyelinase D,[6][7] which is otherwise found only in a few pathogenic bacteria.[8][9] Bites by spiders in this family can produce symptoms ranging from minor localized effects, to severe dermonecrotic lesions, up to and including severe systemic reactions including renal failure, and in some cases, death.[10] Even in the absence of systemic effects, serious bites from sicariid spiders may form a necrotising ulcer that destroys soft tissue and may take months and very rarely years to heal, leaving deep scars. The damaged tissue may become gangrenous and eventually slough away. Initially there may be no pain from a bite, but over time the wound may grow to 10 inches (25 cm) in extreme cases. Bites usually become painful and itchy within two to eight hours, pain and other local effects worsen 12 to 36 hours after the bite, and then necrosis will develop over the next few days.[11]

Systemic effects are unusual but include mild nausea, vomiting, fever, rashes, and muscle and joint pain. Rarely, more severe symptoms occur including red blood cell destruction (hemolysis), low platelets (thrombocytopenia), and loss of clotting factors (disseminated intravascular coagulation).[12] Children may be more susceptible to systemic loxoscelism effects. Deaths have been reported for both the brown recluse and the related South American species Loxosceles laeta and Loxosceles intermedia related to hemolysis and the injury that results to the kidney. Deaths attributed to brown recluse where no brown recluse live, highlight misdiagnosis and misconception[13]

Numerous other spiders have been associated with necrotic bites. The white tailed spider (Lampona spp.) had been suspected in necrotic lesions for decades only to be exonerated by the first extensive review.[14] An early report Sac spider causing necrosis has been frequently referenced.[15] Recent surveys doubt the incidence of necrosis.[16] Necrosis from Hobo spider, a member grass spider family Agelenidae, bite is under the same debate and doubt.[17][18]

Differential diagnosis

The skin manifestations of recluse venom are thought to arise from Sphingomyelinase D. The enzyme acts on cell membranes. The action is therefore limited as the venom can only spread through a set area. The originally red swollen area becomes a dry black ulcer. Skin infections, in particular the widespread methicillin-resistant Staphylococcal aureus, remain swollen and red.[19] Pus forms and the lesion often drains. It can continue to spread and expand as the bacteria grow. Other skin lesions and infections are much more common than spider bites. Physicians have reported brown recluse spider bites where no brown recluse exist.[20] Ed: in 100 pictures retrieved online only 3 were consistent with Sphingomyelinase pathophysiology.

Incidence of severe envenomation

Despite public concern about spider bites, severe envenomation is rare. Few spiders have toxins in sufficient volume to harm people. Of those that do, some have limited habitats. Spider behavior may be caused by limited human interaction. Spider defense against predators include camouflage, and escape by falling or running.[21] Biting is a last resort and the amount of venom injected varies greatly. Spider venom toxicity can be evaluated in experimental animals, or reported from accidental bites. Different experimental animals have different reactions to the same venom. The dose that is lethal to half of the animals poisoned is the LD50 and those values for mice is below. The LD50 of many poisons is known for humans but not that of spider venom.[citation needed]

Serious bites develop symptoms quickly, within the hour. While a serious medical condition may result (see latrodectims and loxocelism) fatalities are exceedingly rare. Appropriate medical treatment can improve speed of recovery. The scenario given in movies such as Arachnophobia, where bite victims die within minutes, does not occur. Small children are considered an exception because the amount of venom dispersed throughout the body is many times the concentration in an adult. There is at least one recorded case of a small child dying within 15 minutes of a bite from a Sydney funnel-web spider; that death occurred before the development of an antivenom. Since the antivenom was developed there have been no fatalities due to this species.

The neurotoxic venoms of the Sydney funnel-web spider and the Brazilian wandering spider are both known to have lethal complications. For the Brazilian wandering spider only 1 out of 200 bites is serious,[22] in part because they appear to be capable of biting without injecting venom.[23] Atrax robustus has a limited distribution and few bites are reported yearly.

The geographical range of the widow spiders is very great. As a result, far more people are exposed, worldwide, to widow bites than any other spider. Widow spiders bites are most often mild but may rarely cause serious complications in people. Fatalities had been reported as high as 5% of bites and as low as 0.2% of bites.[24]

Loxosceles live in areas of South America and the southern United States. There are populations of desert and Arizona recluse in the Western deserts of the United States,[25] but bites are rarely reported from these species. In established areas many spiders may populate the home. Even still the "reclusive" nature of the spider limits true bites.[26] More bites had been reported in Florida than recluses ever found in the area.[27]

Clinical presentation

Genus Species Common name Body length Venom amount LD-50 Alternate LD-50 Deaths reported
Atrax A. robustus Sydney funnel-web spider 24–32 mm.[28] 0.25 mg (F) and 0.81 mg (M) [29] 2 mg [30] 0.16 mg/kg [31] unknown 13 attributed deaths from 1927 to 1980[32]
Hadronyche H. formidabilis Northern tree funnel-web spider 23–45 mm. 1 death.[33] High rates of severe envenoming.[28][34]
Hadronyche H. cerberea Southern tree funnel-web spider High rates of severe envenoming.[34]
Latrodectus L. mactans Black widow 8–15 mm [28] 0.02–.03 mg.[35][36] 0.002 mg/kg [35]* 0.9 mg/kg 36 deaths recorded from 1965 to 1990 in the U.S.
5% of reported bites prior to antivenom availability [28]
Latrodectus L. tredecimguttatus Malmignatte (approx. same) (approx. same) 0.68 μg/kg [37] 16.25 μg/kg [37] possibility of deaths in Southern Europe first attributed to the brown recluse, suggesting larger frequency of the bites.
Loxosceles L. reclusa Brown recluse 1.2 cm (0.75 in) [28] 6–10 mm [28] .13–.27 mg.[37][38] necrosis and amputation of limbs more common, deaths rare[28]
Loxosceles L. intermedia 0.48 mg/kg [39] 0.34 mg/kg (SC)[40]
Loxosceles L. laeta Chilean recluse 1.45 mg/kg [39] High rates of severe envenomation.[41]
Loxosceles L. gaucho 0.74 mg/kg [39]
Phoneutria P. bahiensis Brazilian wandering spider 30 mm 1.079 mg [42] .00061–.00157 mg/kg [42] cardiac failure reported in 5 out of 12 bitten
Phoneutria P. boliviensis Brazilian wandering spider 30 mm 1.079 mg.[42] .00061–.00157 mg/kg [42]
Phoneutria P. fera Brazilian wandering spider 30 mm [28] 1.079 mg [42] .00061–.00157 mg/kg [42] disputed effectiveness of the antivenin – 4 deaths out of 7 administered [28]
Phoneutria P. nigriventer Brazilian wandering spider 3–5 cm (1.25–2 in) [43] 2.15 mg [38] 1.079 mg.[42] 15.20 ng/mg.[38] 00061–.00157 mg/kg [42] 200 µg/kg (0.2 ng/mg) [38] severe cardiac failure, signs of priapism and irreversible damage to the central nervous system recorded.
18 deaths in Brazil alone from 2007 to 2010 [28]
Phoneutria P. reidyi Brazilian wandering spider 30 mm .00061–.00157 mg/kg [42] 0.3 mg/kg
Hexophthalma spp. Six-eyed sand spiders 17 mm large necrotic lesions
Haplopelma H. schmidti (previously H. huwenum, Selenocosmia huwena) Chinese bird spider 0.70 mg/kg [44] 1 death reported of a 5-year-old child suffocated, possibly caused by allergens to the venom.
Poecilotheria P. ornata Fringed ornamental tarantula Instances of coma reported.[45][unreliable source?]
Poecilotheria P. fasciata ** Sri Lankan ornamental tarantula Instances of cardiac failure reported [45][[[Link rot dead link}}]]][unreliable source?]
Cheiracanthium spp. Yellow Sac spider 6–10 mm one case of irreversible damage to the skin reported [28]
Cheiracanthium C. japonicum Japanese sac spider 6–10 mm
Macrothele M. holsti, M. gigas, M. taiwanensis [36] Primitive burrowing spiders No deaths reported in Taiwan.[46]
Steatoda S. grossa Cupboard spider Mild widow-like symptoms reported, no severe consequences
Study suggests its venom can be effective in treating widow bites because of their similarity.

* This value is based on experience with human exposures.
** Several other kinds of tarantulas in the pet trade are regarded as giving non-trivial bites. Tarantulas are typically far larger than spiders with the most toxic kinds of venom. However, the sheer volume of the venom may compensate for its lesser toxicity. The effects of a full envenomation are probably unknown for many species of tarantulas, so due caution is advisable.

References

  1. ↑ "Tarantulas: eight-legged pharmacists and combinatorial chemists". Toxicon 43 (5): 555–74. April 2004. doi:10.1016/j.toxicon.2004.02.007. PMID 15066413. 
  2. ↑ Escoubas P (November 2006). "Molecular diversification in spider venoms: a web of combinatorial peptide libraries". Molecular Diversity 10 (4): 545–54. doi:10.1007/s11030-006-9050-4. PMID 17096075. 
  3. ↑ "Molecular diversification based on analysis of expressed sequence tags from the venom glands of the Chinese bird spider Ornithoctonus huwena". Toxicon 51 (8): 1479–89. June 2008. doi:10.1016/j.toxicon.2008.03.024. PMID 18482741. 
  4. ↑ Diaz, James H (August 1, 2004). "The global epidemiology, syndromic classification, management, and prevention of spider bites". American Journal of Tropical Medicine and Hygiene 71 (2): 239–250. doi:10.4269/ajtmh.2004.71.2.0700239. PMID 15306718. http://www.ajtmh.org/cgi/content/full/71/2/239. 
  5. ↑ Gomez, Marcus V.; Kalapothakis, Evanguedes; Guatimosim, Cristina; Prado, Marco A. M. (2002). "Phoneutria nigriventer Venom: A Cocktail of Toxins That Affect Ion Channels". Cellular and Molecular Neurobiology 22 (5/6): 579–588. doi:10.1023/A:1021836403433. ISSN 0272-4340. PMID 12585681. 
  6. ↑ "Biotechnological applications of brown spider (Loxosceles genus) venom toxins". Biotechnology Advances 26 (3): 210–8. 2008. doi:10.1016/j.biotechadv.2007.12.003. PMID 18207690. 
  7. ↑ "Molecular Evolution, Functional Variation, and Proposed Nomenclature of the Gene Family That Includes Sphingomyelinase D in Sicariid Spider Venoms". Molecular Biology and Evolution 26 (3): 547–66. March 2009. doi:10.1093/molbev/msn274. PMID 19042943. 
  8. ↑ "Sphingomyelinase D from venoms of Loxosceles spiders: evolutionary insights from cDNA sequences and gene structure". Toxicon 45 (5): 547–60. April 2005. doi:10.1016/j.toxicon.2004.11.011. PMID 15777950. 
  9. ↑ "Lateral gene transfer of a dermonecrotic toxin between spiders and bacteria". Bioinformatics 22 (3): 264–8. February 2006. doi:10.1093/bioinformatics/bti811. PMID 16332712. 
  10. ↑ Schenone H; Saavedra T; Rojas A; Villarroel F. (1989). "Loxoscelism in Chile. Epidemiologic, clinical and experimental studies". Revista do Instituto de Medicina Tropical de São Paulo 31 (6): 403–415. doi:10.1590/S0036-46651989000600007. PMID 2577020. http://bases.bireme.br/cgi-bin/wxislind.exe/iah/online/?IsisScript=iah/iah.xis&nextAction=lnk&base=MEDLINE_1966-1995&exprSearch=2577020&indexSearch=UI&lang=i. 
  11. ↑ "Loxoscelism and necrotic arachnidism". J Toxicol Clin Toxicol 21 (4–5): 451–72. 1983–1984. doi:10.3109/15563658308990434. PMID 6381752. 
  12. ↑ Wasserman G (2005). "Bites of the brown recluse spider". N Engl J Med 352 (19): 2029–30; author reply 2029–30. doi:10.1056/NEJM200505123521922. PMID 15892198. 
  13. ↑ "MSU expert hopes to counter brown recluse spider fears". 14 October 2014. http://www.bozemandailychronicle.com/news/montana_state_university/msu-expert-hopes-to-counter-brown-recluse-spider-fears/article_66ce44e2-53fb-11e4-a74b-3744663ed9ca.html. 
  14. ↑ Isbister, GK; Gray, MR (18 August 2003). "White-tail spider bite: a prospective study of 130 definite bites by Lampona species.". The Medical Journal of Australia 179 (4): 199–202. doi:10.5694/j.1326-5377.2003.tb05499.x. PMID 12914510. 
  15. ↑ FURMAN, DP; REEVES, WC (August 1957). "Toxic bite of a spider, Cheiracanthium inclusum Hentz.". California Medicine 87 (2): 114. PMID 13446759. 
  16. ↑ Vetter, RS; Isbister, GK; Bush, SP; Boutin, LJ (June 2006). "Verified bites by yellow sac spiders (genus Cheiracanthium) in the United States and Australia: where is the necrosis?". The American Journal of Tropical Medicine and Hygiene 74 (6): 1043–8. doi:10.4269/ajtmh.2006.74.1043. PMID 16760517. 
  17. ↑ Bennett, R. G.; R. S. Vetter. (2004). "An approach to spider bites: erroneous attribution of dermonecrotic lesions to brown recluse and hobo spider bites in Canada". Canadian Family Physician 50: 1098–1101. PMID 15455808. 
  18. ↑ James H. Diaz, MD (April 1, 2005). "Most necrotic ulcers are not spider bites". American Journal of Tropical Medicine and Hygiene 72 (4): 364–367. doi:10.4269/ajtmh.2005.72.364. 
  19. ↑ Dominguez, TJ (May–June 2004). "It's not a spider bite, it's community-acquired methicillin-resistant Staphylococcus aureus.". The Journal of the American Board of Family Practice 17 (3): 220–26. doi:10.3122/jabfm.17.3.220. PMID 15226288. 
  20. ↑ Vetter, RS; Bush, SP (15 August 2002). "Reports of presumptive brown recluse spider bites reinforce improbable diagnosis in regions of North America where the spider is not endemic.". Clinical Infectious Diseases 35 (4): 442–45. doi:10.1086/341244. PMID 12145729. 
  21. ↑ Pekár, Stano; Hardy, Ian (July 2014). "Comparative analysis of passive defences in spiders (Araneae)". Journal of Animal Ecology 83 (4): 779–790. doi:10.1111/1365-2656.12177. PMID 24205934. 
  22. ↑ Bucaretchi, Fábio; Deus Reinaldo, Cláudia Regina de; Hyslop, Stephen; Madureira, Paulo Roberto; De Capitani, Eduardo Mello; Vieira, Ronan José (2000). "A clinico-epidemiological study of bites by spiders of the genus Phoneutria | BUCARETCHI | Revista do Instituto de Medicina Tropical de São Paulo". Revista do Instituto de Medicina Tropical de São Paulo 42 (1): 17–21. doi:10.1590/S0036-46652000000100003. PMID 10742722. http://www.revistas.usp.br/rimtsp/article/view/30402. Retrieved 14 February 2015. 
  23. ↑ Vital-Brazil, O.; Bernardo-Leite, G.B. & Fontana, M.D. (1988) Modo de ação da peçonha da aranha armadeira, Phoneutria nigriventer (Keiserling, 1891), nas aurículas isoladas de cobaia. Ciênc. Cult., 40: 181-185
  24. ↑ Bettini S (1964). "Epidemiology of Latrodectism". Toxicon 2 (2): 93–102. doi:10.1016/0041-0101(64)90009-1. PMID 14301291. 
  25. ↑ "5 Lies About the Brown Recluse Spider". http://insects.about.com/od/spiders/tp/brown-recluse-lies.htm. 
  26. ↑ Vetter, Richard S.; Barger, Diane K. (1 November 2002). "An Infestation of 2,055 Brown Recluse Spiders (Araneae: Sicariidae) and No Envenomations in a Kansas Home: Implications for Bite Diagnoses in Nonendemic Areas". Journal of Medical Entomology 39 (6): 948–951. doi:10.1603/0022-2585-39.6.948. PMID 12495200. 
  27. ↑ Vetter, Richard S.; Edwards, G. B.; James, Louis F. (1 July 2004). "Reports of Envenomation by Brown Recluse Spiders (Araneae: Sicariidae) Outnumber Verifications of Loxosceles Spiders in Florida". Journal of Medical Entomology 41 (4): 593–597. doi:10.1603/0022-2585-41.4.593. PMID 15311449. 
  28. ↑ 28.00 28.01 28.02 28.03 28.04 28.05 28.06 28.07 28.08 28.09 28.10 Vetter, Richard S.; Isbister, Geoffrey K. (2008). "Medical Aspects of Spider Bites". Annual Review of Entomology 53: 409–29. doi:10.1146/annurev.ento.53.103106.093503. PMID 17877450. 
  29. ↑ "Atrax Robustus". IPCS INCHEM. International Programme on Chemical Safety. 1989. http://www.inchem.org/documents/pims/animal/atrax.htm. 
  30. ↑ Sutherland SK; Duncan AW; Tibballs J. (1980-10-18). "Local inactivation of funnel-web spider (Atrax robustus) venom by first-aid measures: potentially lifesaving part of treatment". Medical Journal of Australia 2 (8): 435–437. doi:10.5694/j.1326-5377.1980.tb131912.x. PMID 7207322. 
  31. ↑ "A comparative study of properties and toxic constituents of funnel web spider (Atrax) venoms". Comparative Biochemistry and Physiology 78 (1): 55–68. 1984. doi:10.1016/0742-8413(84)90048-3. PMID 6146485. 
  32. ↑ Manson's tropical diseases By Gordon C. Cook, Patrick Manson, Alimuddin Zumla, p. 592
  33. ↑ CSIRO (15 May 2012). "Funnel-web spider". CSIRO website. http://www.csiro.au/Outcomes/Environment/Biodiversity/Funnelweb-Spider-Facts.aspx. 
  34. ↑ 34.0 34.1 "Funnel-web spider bite: a systematic review of recorded clinical cases". Med J Aust 182 (8): 407–11. 2005. doi:10.5694/j.1326-5377.2005.tb06760.x. PMID 15850438. https://www.mja.com.au/journal/2005/182/8/funnel-web-spider-bite-systematic-review-recorded-clinical-cases?iframe=true. 
  35. ↑ 35.0 35.1 Stewart, Charles (1998). Beyond the Road: Environmental Emergencies for Emergency Service Providers. Charles Stewart and Associates. http://www.storysmith.net/Articles/Bites%20and%20stings.pdf. Retrieved 2015-02-14. 
  36. ↑ 36.0 36.1 http://www.thudiv.com/variety/spider/spider1.htm) (Tung Hai University, Taiwan, article in Chinese broken link)
  37. ↑ 37.0 37.1 37.2 Ori, Masahisa; Ikeda, Hiroyoshi (1998). "Spider Venoms and Spider Toxins". Journal of Toxicology: Toxin Reviews 17 (3): 405–426. doi:10.3109/15569549809040401. http://homepage3.nifty.com/~hispider/spidervenom.txt. Retrieved 2015-02-14. 
  38. ↑ 38.0 38.1 38.2 38.3 M. F. Manzoli-Palma; N. Gobbi; M. S. Palma (2003). "Insects as biological models to assay spider and scorpion venom toxicity". Journal of Venomous Animals and Toxins Including Tropical Diseases 9 (2): 174–185. doi:10.1590/S1678-91992003000200004. 
  39. ↑ 39.0 39.1 39.2 "Identification and neutralization of biological activities in the venoms of Loxosceles spiders". Brazilian Journal of Med Biol Res 29 (11): 1491–7. November 1996. PMID 9196551. 
  40. ↑ "Loxosceles intermedia ~ VenomZone page". https://venomzone.expasy.org/3596. 
  41. ↑ Fingermann, Matías; De Roodt, Adolfo Rafael; Cascone, Osvaldo; Miranda, María Victoria (2020-06-01). "Biotechnological potential of Phospholipase D for Loxosceles antivenom development" (in en). Toxicon: X 6: 100036. doi:10.1016/j.toxcx.2020.100036. ISSN 2590-1710. PMID 32550591. 
  42. ↑ 42.0 42.1 42.2 42.3 42.4 42.5 42.6 42.7 42.8 "Intersexual variations in the venom of the Brazilian 'armed' spider Phoneutria nigriventer (Keyserling, 1891)". Toxicon 40 (10): 1399–406. 2002. doi:10.1016/S0041-0101(02)00136-8. PMID 12368110. 
  43. ↑ Lelle Petterson. "The genus Phoneutria, Perty 1833, wandering spiders". Minax tarantulas. http://www.minaxtarantulas.net/artiklar/phoneutria/phoneutria_e.html. 
  44. ↑ "Properties and amino acid sequence of huwentoxin-I, a neurotoxin purified from the venom of the Chinese bird spider Selenocosmia huwena". Toxicon 31 (8): 969–78. August 1993. doi:10.1016/0041-0101(93)90256-I. PMID 8212049. 
  45. ↑ 45.0 45.1 http://www.spidertalk.net/SpiderTalk/post.php?action=reply&fid=1&tid=2165&repquote=16279 [|permanent dead link|dead link}}]
  46. ↑ Hung, Shin-Wen; Wong, Tzong-Leun. "Arachnid Envenomation in Taiwan". Ann. Disaster Med. 3 (Suppl. 1): S12–S17. http://www.disaster.org.tw/chinese/annmed/Vol3supp1/3.pdf. 



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