Unintentional Intoxications of Nonhuman Primates: Phytotoxins and Pesticides: Comparison
View Latest Version
Please note this is a comparison between Version 2 by Conner Chen and Version 1 by Jaco Bakker.

Wild and captive nonhuman primates (NHP) are exposed and potentially vulnerable to many natural and man-made toxic threats. Nevertheless, wild NHP are capable of coping with these threats using strategies, namely avoidance, dilution, gastrointestinal degradation, or detoxification, which require genetic potential, learning from parents and conspecifics in their social group, or prior experience through random food sampling and experimentation. Captive NHP are also at high risk for intoxications when they are often housed in an outdoor enclosure in a vivarium or zoo that is in or close to a large urban and industrial city. These NHP are potentially exposed to urban-industrial air pollution due to industrial and vehicle exhausts, waste incineration, and the domestic and industrial use of petroleum-based products, cleaners, pesticides, and paints, amongst others. 

  • nonhuman primates
  • poisoning

1. Phytotoxins

Phytotoxins are natural compounds that are inherently abundant in plants and are synthesized by plants to protect themselves against predators, insects, and microorganisms or in response to environmental stress. Phytotoxins can also underlie a plant’s characteristics, such as its aroma, color, and flavor. The chemical or molecular structure of phytotoxins is diverse and encompasses alkaloids, terpenes, phenylpropanoids, and polyketoids. Poisonous plants are classified according to the chemical nature of their phytotoxin(s), their phylogenetic relationships, or their botanical characteristics.
Although NHP are omnivores, they spend most of their waking time foraging and searching for and processing food. Phytotoxin poisoning in NHP occurs after ingesting plants that are not intended for eating. Accordingly, NHP can be poisoned after ingesting a toxic plant because (a) hunger may cause them to graze a plant that would not be eaten under normal circumstances, or (b) they are undernourished and ingest a toxic plant to provide caloric intake. The consequences on the health of NHP after ingesting a toxic plant can range from none to sudden death. This large in-between range of adverse consequences comprises clinical signs of liver or kidney damage, cardiovascular, nervous system, musculoskeletal or gastrointestinal problems, allergic reactions, birth defects, and reproductive failure.
Most reports of phytotoxin poisoning describe such poisonings in captive NHP (Table 21). Descriptions of phytotoxin poisoning in wild NHP have not been reported because they have developed strategies to cope or avoid this toxic threat, namely avoidance, dilution, gastrointestinal degradation, or detoxification. For example, Zanzibar red colobus monkeys (Procolobus kirkii) eat the charcoal from burnt trees. This behavior is thought to be a learned behavior for counteracting the toxicity of phenols in the Indian almond and mango leaves, which constitute a major part of their diet [20][1]. Black-and-white colobus monkeys (Colobus guereza) frequently come to ground to eat water plants and clay [21][2]. Although water–plant consumption may remedy mineral deficiencies [22][3], the clay may be consumed to adsorb plant toxins (usually noxious phenols) and promote their excretion, in addition to adjusting the pH of the forestomach.
Table 21.
 Cases of unintentional phytotoxin poisoning in captive NHP.
NHP Species Plant Species Phytotoxin Clinical Signs Clinical Signs Reference
Varecia Variegate Variegate)
Hairy nightshade (
Solanum sarrachoides
) Alkaloid

glycoside		 Acute death or less active and partial inappetence for 48 h followed by depression, lethargy, ataxia, diarrhea, and slow pupillary reflexes prior to death acute, severe, diffuse hemorrhagic enteritis and typhlitis and a small volume of unidentifiable plant material was found in the stomach contents Drew & Fowler, 1991 [28]Drew & Fowler, 1991 [8]
Wild NHP consume many types of plant materials that are native to the regions in which they live. This plant material, referred to as browse, is an important part of the diet of captive NHP. To date, little research has been conducted to substantiate the safety of browse species for captive NHP. The National Research Council of the National Academies has published a list of NHP-safe plants that can be used for browse [23][9]. However, the authors of the list do not guarantee the safety of ingesting these plants.
Table 2 summarizes the published reports of unintentional phytotoxin poisoning in captive NHP. No antidote or specific treatments for the poisonings were provided because the poisonings were not recognized before death.

2. Pesticides

A pesticide is a naturally occurring or synthetic chemical or biological agent that is used to control pests. About 700 pesticides are in current use and these pesticides can be classified according to (a) the type of target pest (organism), such as a herbicide, an insecticide, a nematicide, a rodenticide, a fungicide, and a bactericide; (b) the chemical structure, such as organophosphates, organochlorines, carbamates, and pyrethroids; and (c) the mechanism (mode) of action, such as enzyme inhibitors, disruptors of cellular signaling pathways, and generators of reactive molecules that destroy cellular components, amongst others. To be acceptable, a pesticide must be toxic to the intended target and not toxic to any non-target organism.
Wilderness areas are vital refuges where natural ecological and evolutionary processes can operate with minimal human disturbance. Humans have appropriated much land and altered terrestrial ecosystems for agriculture. Agricultural frontiers are dynamic environments that are characterized by the conversion of native habitats to agriculture and the highest incidence of species loss occurs on an agricultural frontier. Therefore, habitat loss is a burgeoning threat to a population of wild NHP and other terrestrial vertebrates that live on an agricultural frontier. Furthermore, the use of pesticides on an agricultural frontier has the potential to detrimentally affect wild NHP populations, the local biodiversity, and ecosystem’s structure and function.
An overview of the reported cases of pesticide poisonings in wild NHP are presented in Table 32A,B. Since these poisonings occurred mostly on agricultural frontiers, pesticides, which were used to control agricultural pests, were the suspected cause of these poisonings in non-target wild NHP. The main reported outcome of an acute poisoning by a pesticide was death (Table 32A). Continual exposure to a pesticide on an agricultural frontier may also be hazardous for wild NHP populations because of the possible teratogenic effects of the pesticide: birth (congenital) defects have been reported in the offspring of pesticide-exposed pregnant mothers (Table 32B). These effects were usually documented in the reports of research projects whose aims were to (a) determine the cause of the phenotypical harm to wild NHP and (b) understand whether these harms were linked to environmental pollution of their habitat. Unfortunately, no definitive links between pesticide exposure and reproduction or frequency of stillbirths could be made. Interestingly, many health authorities advise pregnant women or women who are planning to become pregnant avoid contact with or exposure to pesticides because some pesticides may cross the placental barrier and lead to miscarriages, pre-term births, infants with low birth weights, birth defects, and congenital anomalies.
Table 32. (A) Summary of the reported cases of death in wild NHP due to acute pesticide poisoning on agricultural frontiers. (B) Summary of the reported birth defects and congenital anomalies in wild NHP due to suspected continual pesticide exposure on agricultural frontiers. * The clinical signs and main laboratory findings and pathology were often not performed and documented in the report.
(A)
NHP Species Suspected Pesticide Clinical Signs Laboratory and Main Postmortem Findings Reference
Not specified Anticoagulant

rodenticide		 Not provided Not performed Bates, 2016 [29]Bates, 2016 [10]
Vervet monkeys (Chlorocebus pygerythrus) Aldicarb, carbofuran Sudden death Not performed Botha et al., 2015 [30]Botha et al., 2015 [11]
Golden Langurs (Trachypithecus geei) Organochlorine

insecticide		 Sudden death Insecticide was detected in the liver, kidney, and intestinal contents Pathak, 2011 [31]Pathak, 2011 [12]
Bonnet macaque (Macaca radiata) Carbofuran (a

carbamate insecticide)		 Sudden death Cyanosis, severe pulmonary congestion, splenomegaly and dark purplish-blue granules, identified as carbofuran, in the gastric contents Radhakrishnan, 2017, 2018 [32,33]Radhakrishnan, 2017, 2018 [13][14]
Cynomolgus monkeys (Macaca fascicularis) Anticoagulant bromadiolone and

difenacoum		 Sudden death extensive subcutaneous and internal hemorrhages. Bromadiolone and difenacoum were detected in frozen liver samples IJzer et al., 2009 [34]IJzer et al., 2009 [15]
Squirrel Monkey (Saimiri sciureus) Fipronil Ranging from sudden death to symptoms of depression, inappetence, lethargy and body weight loss, which progressively disappear over time Fipronil and fipronil sulfone were detected in cutaneous and brain tissue Demir et al., 2021 [35]Demir et al., 2021 [16]
Tantalus monkeys (Cercopithecus aethiops) Dieldrin Sudden death Not performed Koeman et al., 1978 [36]Koeman et al., 1978 [17]
(B)
NHP Species Suspected Pesticide Clinical Signs Laboratory and Main Postmortem Findings Reference
Ring-tailed lemurs Organochlorine

pesticides		 * * Rainwater et al., 2009 [37];

Dutton et al., 2003 [38]; Miller et al., 2007 [39]		Rainwater et al., 2009 [18];

Dutton et al., 2003 [19]; Miller et al., 2007 [20]
Chimpanzees and baboons Several different pesticides (Congenital) facial and nasal deformities (i.e., reduced nostrils, cleft lip), limb deformities, reproductive problems, and hypopigmentation * Krief et al., 2017 [40]; Lacroux et al., 2019 [41]Krief et al., 2017 [21]; Lacroux et al., 2019 [22]
Baboons, howler monkeys, chimpanzees, red-tailed monkeys, red colobus Pesticides,

halogenated flame retardants, and

organophosphate flame retardants		 * * Wang et al., 2020 [42]Wang et al., 2020 [23]
Douc langurs (Pygathrix spp.) Dioxins (i.e., Agent Orange, tetrachlorodibenzo-p-dioxin) and dioxin-related compounds Two animals exhibited developmental consequences of possible dioxin exposure * Brockman et al., 2009 [43];

Brockman & Harrison, 2013 [44]		Brockman et al., 2009 [24];

Brockman & Harrison, 2013 [25]
Baboons (Papio spp.), Tantalus monkeys (Chlorocebus tantalus), red tail monkeys (Cercopithecus ascanius), vervet monkeys (C. pygerythrus), Campbell’s monkeys (Cercopithecus campbelli lowei), Zanzibar red colobus (Procolobus kirkii), and chimpanzees (Pan troglodytes) Pesticides * * Ogada, 2014 [45]; Naughton-Treves, 1998 [46];

Eniang et al., 2011 [47]; Nowak et al., 2009 [48]; Sai et al., 2006 [49]		Ogada, 2014 [26]; Naughton-Treves, 1998 [27];

Eniang et al., 2011 [28]; Nowak et al., 2009 [29]; Sai et al., 2006 [30]
Japanese monkeys (Macaca fuscata) Dieldrin and heptacholorepoxide Congenital defects such as abnormal limbs in offspring Elevated concentration of dieldrin and heptacholorepoxide in the liver and kidney of female monkeys whose babies were born with malformations Minezawa et al., 1990 [50]Minezawa et al., 1990 [31]
Cebus apella English ivy (Hedra helix)   Severe gastroenteritis resulting in acute death Not performed Fowler, 1981 [24]Fowler, 1981 [4]
White mantled-black colobus (Colobus guereza) Alleghany (Viburnum x rhytidophylloides)   Pain, lethargy, inappetence, unable to climb, vomiting, diarrhea resulting in death Small spicules of plant material were present in the inflammatory exudate associated with the stomach’s mucosa Irlbeck et al., 2001 [25]Irlbeck et al., 2001 [5]
François’ langurs (Trachypithecus francoisi) Hybrid yew shrub (Taxus baccata X T. cuspidata) Taxine

alkaloids		 Found dead without previous clinical signs Multiple yew fragments in gastric content and taxine alkaloids were detected by gas chromatography and mass spectrometry of the gastric contents Lacasse et al., 2007 [26]Lacasse et al., 2007 [6]
Alaotran gentle lemur (Hapalemur griseus alaotrensis) Russian vine (Polygonum baldschuanicum) Oxalate Varying degrees of lethargy, inappetence, abdominal discomfort and diarrhea progressing to signs of renal insufficiency (hematuria, proteinuria, and severe uremia) resulting in death Chronic renal failure, presence of calcium oxalate crystals in the renal tubules Scott, 1996 [27]Scott, 1996 [7]
black and white ruffed lemurs (

References

  1. Struhsaker, T.T.; Cooney, D.O.; Siex, K.S. Charcoal consumption by Zanzibar Red Colobus monkeys: Its function and its ecological and demographic consequence. Int. J. Primatol. 1997, 18, 61–72.
  2. Oates, J.F. Water-Plant and Soil Consumption by Guereza Monkeys (Colobus guereza): A Relationship with Minerals and Toxins in the Diet? Biotropica 1978, 10, 241–253.
  3. Reynolds, V.; Lloyd, A.W.; English, C.J.; Lyons, P.; Dodd, H.; Hobaiter, C.; Newton-Fisher, N.; Mullins, C.; Lamon, N.; Schel, A.M.; et al. Mineral Acquisition from Clay b.by Budongo Forest Chimpanzees. PLoS ONE 2015, 10, e0134075.
  4. Fowler, M.E. Plant Poisoning in Captive Nondomestic Animals. J. Zoo Anim. Med. 1981, 12, 134–137.
  5. Irlbeck, N.A.; Knightly, F.; Kenny, D.; Moore, M.M.; Getzy, D.M. Ingestion of Viburnum x rhytidophylloides ‘Alleghany’ potentially lethal to White-Mantled Black Colobus (Colobus guereza). In Proceedings of the Fourth Conference on Zoo and Wildlife Nutrition, AZA Nutrition Advisory Group, Lake Buena Vista, FL, USA, 19–23 September 2001.
  6. Lacasse, C.; Gamble, K.C.; Poppenga, R.H.; Farina, L.L.; Landolfi, J.; Terio, K. Taxus sp. intoxication in three Francois’ langurs (Trachypithecus francoisi). J. Vet. Diagn. Investig. 2007, 19, 221–224.
  7. Scott, D.P. CASE IV-NR1577/95 (AFIP 2506276). In Proceedings of the AFIP: Wednesday Slide Conference No. 20, Washington, DC, USA, 13 March 1996.
  8. Drew, M.L.; Fowler, M.E. Poisoning of Black and White Ruffed Lemurs (Varecia variegata variegata) by Hairy Nightshade (Solanum sarrachoides). J. Zoo Wildl. Med. 1991, 22, 494–496.
  9. National Research Council. Nutrient Requirements of Nonhuman Primates: Second Revised Edition; The National Academies Press: Washington, DC, USA, 2003; p. 306.
  10. Bates, N. Anticoagulant Rodenticide Exposure in Animals. Submission from the Veterinary Poisons Information Service; VPIS: London, UK, 2016.
  11. Botha, C.J.; Coetser, H.; Labuschagne, L.; Basson, A. Confirmed organophosphorus and carbamate pesticide poisonings in South African wildlife (2009–2014). J. S. Afr. Vet. Assoc. 2015, 86, 1329.
  12. Pathak, D.C. Organochlorine insecticide poisoning in Golden Langurs Trachypithecus geei. J. Threat. Taxa 2011, 3, 1959–1960.
  13. Radhakrishnan, S. Wildlife poisoning in Kerala, South India: The canary in the coal mine? In Proceedings of the 66th Wildlife Disease Association Annual International Conference, San Cristobal de las Casas, Mexico, 23–28 July 2017.
  14. Radhakrishnan, S. A note on wildlife poisoning cases from Kerala, South India. Eur. J. Wildl. Res. 2018, 64, 58.
  15. IJzer, J.; Kik, M.; Keehnen-Anema, M.C. Unintentional lethal rodenticide poisoning in 8 young macaques (macaca fascicularis) plus 3 possible survivors. Curiosity killed the macaque. In Proceedings of the International Conference on Diseases of Zoo and Wild Animals, Hilvarenbeek, The Netherlands, 20–24 May 2009.
  16. Demir, O.; Özdemir, Ö.; Koçak, A.; Arslan, Z.; Sevin, S. Acute fipronil intoxication in Squirrel Monkey (Saimiri sciureus). Ank. Üniversitesi Vet. Fakültesi Derg. 2021, 68, 181–184.
  17. Koeman, J.H.; Den Boer, W.M.J.; Feith, A.F.; de Iongh, H.H.; Spliethoff, P.C.; Na’isa, B.K.; Spielberger, U. Three years’ observation on side effects of helicopter applications of insecticides used to exterminate Glossina A species in Nigeria. Environ. Pollut. 1970, 15, 31–59.
  18. Rainwater, T.R.; Sauther, M.L.; Rainwater, K.A.; Mills, R.E.; Cuozzo, F.P.; Zhang, B.; McDaniel, L.N.; Abel, M.T.; Marsland, E.J.; Weber, M.A.; et al. Assessment of organochlorine pesticides and metals in ring-tailed lemurs (Lemur catta) at Beza Mahafaly Special Reserve, Madagascar. Am. J. Primatol. 2009, 71, 998–1010.
  19. Dutton, C.J.; Junge, R.E.; Louis, E.E. Biomedical evaluation of free-ranging ring-tailed lemurs (Lemur catta in Tsimanampetsotsa Strict Nature Reserve, Madagascar. J. Zoo Wildl. Med. 2003, 34, 16–24.
  20. Miller, D.S.; Sauther, M.L.; Hunter-Ishikawa, M.; Fish, K.; Culbertson, H.; Cuozzo, P.F.; Campbell, T.W.; Andrews, G.A.; Chavey, P.S.; Nachreiner, R.; et al. Biomedical evaluation of free-ranging ring-tailed lemurs (Lemur catta) in three habitats at the Beza Mahafaly Special Reserve, Madagascar. J. Zoo Wildl. Med. 2007, 38, 201–216.
  21. Krief, S.; Berny, P.; Gumisiriza, F.; Gross, R.; Demeneix, B.; Fini, J.B.; Chapman, C.A.; Chapman, L.J.; Seguya, A.; Wasswa, J. Agricultural expansion as risk to endangered wildlife: Pesticide exposure in wild chimpanzees and baboons displaying facial dysplasia. Sci. Total Environ. 2017, 598, 647–656.
  22. Lacroux, C.; Guma, N.; Krief, S. Facial dysplasia in wild forest olive baboons (Papio anubis) in Sebitoli, Kibale National Park, Uganda: Use of camera traps to detect health defects. J. Med. Primatol. 2019, 48, 143–153.
  23. Wang, S.; Steiniche, T.; Rothman, J.M.; Wrangham, R.W.; Chapman, C.A.; Mutegeki, R.; Quiros, R.; Wasserman, M.D.; Venier, M. Feces are Effective Biological Samples for Measuring Pesticides and Flame Retardants in Primates. Environ. Sci. Technol. 2020, 54, 12013–12023.
  24. Brockman, D.; Harrison, R.; Nadler, T. Conservation of douc langurs in Vietnam: An assessment of Agent Orange exposure in douc langurs (Pygathrix) at the Endangered Primate Rescue Center, Cuc Phuong National Park, Vietnam. Vietnam. J. Primatol. 2009, 3, 45–64.
  25. Brockman, D. Agent orange exposure in black-shanked douc langurs (Pygathrix nigripes) at Nam Cat Tien National Park, Vietnam. Vietnam. J. Primates 2013, 2, 49.
  26. Ogada, D.L. The power of poison: Pesticide poisoning of Africa’s wildlife. Ann. N. Y. Acad. Sci 2014, 1322, 1–20.
  27. Naughton-Treves, L. Predicting Patterns of Crop Damage by Wildlife around Kibale National Park, Uganda. Conserv. Biol. 1998, 12, 156–168.
  28. Eniang, E.A.; Ijeomah, H.M.; Okeyoyin, G.; Uwatt, A.E. Assessment of human-wildlife conflicts in Filinga Range of Gashaka Gumti National Park, Nigeria. PAT 2011, 7, 15–35.
  29. Nowak, K.; Perkin, A.; Jones, T. Update on Habitat Lossand Conservation Statusof the Endangered Zanzibar Red Colobus on Uzi and Vundwe Islands; Technical report; Department of Commercial Crops, Fruits and Forestry: Zanzibar, Tanzania, 2009; p. 22.
  30. Saj, T.L.; Mather, C.; Sicotte, P. Traditional taboos in biological conservation: The case of Colobus vellerosus at the Boabeng-Fiema Monkey Sanctuary, Central Ghana. Soc. Sci. Inf. 2006, 45, 285–310.
  31. Minezawa, M.; Nozawa, K.; Gotoh, S.; Yoshihiro, S.; Hamada, Y.; Inagaki, H.; Nigi, H. A cytogenetic study on congenital limb malformations in the Japanese monkey (Macaca fuscata). Primates 1990, 31, 571–577.
More
© Text is available under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/)
ScholarVision Creations
Feedback