Toxoplasma gondii in Sheep and Goats from Central Iran

Abstract Objective Toxoplasmosis, caused by Toxoplasma gondii, infects humans by consuming infected raw or undercooked meat and foods harboring mature oocysts. In this study, we assessed the prevalence of T. gondii in sheep and goats coming from central Iran. After completing the questionnaire, about one gram of liver or diaphragm tissue was taken as a sample from 90 sheep and 90 goats slaughtered in Yazd Province and stored at – 20 ºC. DNA extraction was done, and then T. gondii was detected using nested PCR. Results This study indicated that the prevalence of T. gondii in all slaughtered animals was 11.6% (21 of 180), including 14.4% (13/90) in sheep and 8.8% (8/90) in goats. The infection rates in liver and diaphragm samples were 12.2% (11/90) and 11.1% (10/90), respectively (p = 0.8163). The infection rate in animals older than one was 16.3% (15/92), and it was 6.8% (6/88) in animals under one year of age. Therefore, no significant differences were found (p = 0.475). Infection rates were 19.5% (18/92) in males and 3.4% (3/88) in females (p = 0.0007). In conclusion, the infection rates of toxoplasmosis in livestock in this area are almost high, and therefore, it is necessary to design appropriate prevention programs to control the disease.

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Genetic Diversity of Toxoplasma Gondii by Serological and Molecular Analyzes in Different Sheep and Goat Tissues in Northeastern Iran

10.21203/rs.3.rs-853244/v1 ◽

2021 ◽

Author(s):

Nima Firouzeh ◽

Hamid Foroughiborj ◽

Naser ziaali ◽

Amir Tavakoli Kareshk

Keyword(s):

Toxoplasma Gondii ◽

Nested Pcr ◽

Sequencing Analysis ◽

Serum Samples ◽

Preventive Program ◽

Sheep And Goats ◽

Route Of Transmission ◽

B1 Gene ◽

Undercooked Meat ◽

Gra6 Gene

Abstract Background: Toxoplasmosis, a parasitic disease caused by compilation protozoan agent Toxoplasma gondiithat led to significant financial and quality-adjusted life-year losses. Consumption of undercooked or raw meat has been regarded as a major route of transmission. The present study was conducted to determine the seroposevitity rate of T.gondii in sheep and goats by serological and molecular tests and also genotyping of obtained isolatesin northeast of Iran.Methods: Blood and tissue samples (diaphragm, heart) of 296 animals (including 168 sheep and 128 goats) were collected from slaughterhouse in Quechan city from august 2016 to April 2017. Serum samples examined by the Modified agglutination test (MAT) and the Nested-PCR method performed to amplify the fragment of the B1 gene to detect parasite DNA on diaphragm and heart tissues of seropositive animals. PCR-RFLP method of GRA6 gene was used to determine the genotype of T. gondii. Also, sequencing analysis was performed to evaluate the Toxoplasma type strains. Results: Serum positive for MAT results were found in 27.4% (46/168) of Sheep and23.4% (30/128) of goats. Positive Nested-PCR of B1 gene results in diaphragm and heart tissues of sheep and goats was 47.8% (22/46) and 26.1% (12/46), 40% (12/30) and 23.3% (7/30), respectively. Nested-PCR of GRA6 gene results were positive in 10 samples (7 sheep and 3 goats) that RFLP technique results with using MseІ enzyme revealed genotype І. Sequencing and Phylogenetic analysis revealed DNA of all samples were closely related to Toxoplasma type І.Conclusions: Concerning to highseropositivityrate of toxoplasmosis in studied region, undertaking an appropriate preventive program for reducing the prevalence of T. gondii infection by raw or undercooked meat consumption of livestock recommended. Our study supports the notion that consumption of raw and undercooked meat of these animals can be a probable source of human toxoplasmosis.

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Seroprevalence of Toxoplasma gondii in Dairy Cattle with Reproductive Problems in Sudan

ISRN Veterinary Science ◽

10.1155/2013/895165 ◽

2013 ◽

Vol 2013 ◽

pp. 1-4 ◽

Cited By ~ 12

Author(s):

Abdelghafar M. Elfahal ◽

Amira M. Elhassan ◽

Mohammed O. Hussien ◽

Khalid A. Enan ◽

Azza B. Musa ◽

...

Keyword(s):

Toxoplasma Gondii ◽

Dairy Cattle ◽

Age Groups ◽

Parasitic Infections ◽

Age Group ◽

Infection Rates ◽

Herd Level ◽

Individual Level ◽

Reproductive Disease ◽

One Year

Toxoplasmosis, caused by Toxoplasma gondii, is one of the most common parasitic infections of humans and other warm-blooded animals in most parts of the world. The disease is common among sheep and goats and it is recognized as one of the major causes of reproductive failure in these animals. Cattle, on the other hand, can be infected, but abortion or perinatal mortality has not been recorded. This survey was carried out to study the prevalence of this disease in cattle in Khartoum and Gazira States (Sudan). 181 sera samples collected from dairy cattle with reproductive problems were assayed for antibodies to T. gondii by ELISA. The prevalence rate of T. gondii antibodies in cattle at herd level was 44.8% (13/29). Herd level infection rates were 50% and 33.3% in Khartoum and Gazira States, respectively. The overall prevalence of T. gondii at individual level in both states was 13.3% (24/181). The prevalence was 12.7% (17/134), was 14.9% (7/47) in Khartoum and Gazira State, respectively. There was significantly higher (P<0.05) prevalence of T. gondii antibodies in the age group less than one year old (36.4%) than in other age groups and in males (30.8%) than in females (11.9%) while no significant relationship was discerned regarding breed, location, season, or signs of reproductive disease.

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Apparent density, trypanosome infection rates and host preference of tsetse flies in the sleeping sickness endemic focus of Northwestern Uganda

10.21203/rs.3.rs-43888/v3 ◽

2020 ◽

Author(s):

Robert Opiro ◽

Robert Opoke ◽

Harriet Angwech ◽

Esther Nakafu ◽

Francis A. Oloya ◽

...

Keyword(s):

Infection Rate ◽

Apparent Density ◽

Blood Meal ◽

Nested Pcr ◽

Tsetse Fly ◽

Tsetse Flies ◽

Trypanosome Species ◽

Trypanosome Infection ◽

Infection Rates ◽

Monitor Lizard

Abstract Background: African trypanosomiasis, caused by protozoa of the genus Trypanosoma and transmitted by the tsetse fly, is a serious parasitic disease of humans and animals. Reliable data on the vector distribution, feeding preference and the trypanosome species they carry is pertinent to planning sustainable control strategies.Methodology: We deployed 109 biconical traps in 10 villages in two districts of northwestern Uganda to obtain information on the apparent density, trypanosome infection rates and blood meal sources of tsetse flies. A subset (272) of the collected samples was analyzed for detection of trypanosomes species and sub-species using a nested PCR protocol based on primers amplifying the Internal Transcribed Spacer (ITS) region of ribosomal DNA. 34 blood-engorged adult tsetse midguts were analyzed for blood meal sources by sequencing of the mitochondrial cytochrome c oxidase 1 (COI) and cytochrome b (cytb) genes. Results: Out of the 109 traps deployed, we captured 622 Glossina fuscipes fuscipes tsetse flies (269 males and 353 females). Apparent density (AD) ranged from 0.6 to 3.7 flies/trap/day in the two districts. 29 (10.7%) of the flies were infected with one or more trypanosome species. Infection rate was not significantly associated with neither age group (χ2 = 5.001, df=2, 0.082), sex of the fly (χ2 = 0.099, df = 1, p = 0.753), district of origin (χ2= 0.629, df = 1, p = 0.428) nor village (χ2= 9.252, df = 9, p = 0.414). Nested PCR revealed several species of trypanosomes: T. vivax (6.62%), T. congolense (2.57%), T. brucei and T. simiae each at 0.73%. Blood meal analyses revealed five principal vertebrate hosts, namely, cattle (Bos taurus), humans (Homo sapiens), Nile monitor lizard (Varanus niloticus), African mud turtle (Pelusio schapini) and the African Savanna elephant (Loxodonta africana).Conclusion: We found an infection rate of 10.78 %, with all infections attributed to trypanosome species that are causative agents for the animal disease only. However, more verification of this finding using large-scale passive and active screening of human and tsetse samples should be done. Cattle and humans appear to be the most important tsetse hosts in the region and should be considered in the design of interventions.

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Apparent density, trypanosome infection rates and host preference of tsetse flies in the sleeping sickness endemic focus of Northwestern Uganda

10.21203/rs.3.rs-43888/v2 ◽

2020 ◽

Author(s):

Robert Opiro ◽

Robert Opoke ◽

Harriet Angwech ◽

Esther Nakafu ◽

Francis A. Oloya ◽

...

Keyword(s):

Infection Rate ◽

Apparent Density ◽

Blood Meal ◽

Nested Pcr ◽

Large Scale ◽

Tsetse Fly ◽

Tsetse Flies ◽

Trypanosome Species ◽

Infection Rates ◽

Monitor Lizard

Abstract Background: African trypanosomiasis, caused by protozoa of the genus Trypanosoma and transmitted by the tsetse fly, is a serious parasitic disease of humans and animals. Reliable data on the vector distribution, feeding preference and the trypanosome species they carry is pertinent to planning sustainable control strategies.Methodology: We deployed 109 biconical traps in 10 villages in two districts of northwestern Uganda to obtain information on the apparent density, infection rates and blood meal sources of tsetse flies. A subset (272) of the collected samples was analyzed for detection of trypanosomes species and sub-species using a nested PCR protocol based on primers amplifying the Internal Transcribed Spacer (ITS) region of ribosomal DNA. 34 blood-engorged adult tsetse midguts were analyzed for blood meal sources by sequencing of the mitochondrial cytochrome c oxidase 1 (COI) and cytochrome b (cytb) genes. Results: Out of the 109 traps deployed, we captured 622 Glossina fuscipes fuscipes tsetse flies (269 males and 353 females). Apparent density (AD) ranged from 0.6 to 3.7 flies/trap/day in the two districts. 29 (10.7%) of the flies were infected with one or more trypanosome species. Infection rate was not significantly associated with neither age group (χ2 = 5.001, df=2, 0.082), sex of the fly (χ2 = 0.099, df = 1, p = 0.753), district of origin (χ2= 0.629, df = 1, p = 0.428) nor village (χ2= 9.252, df = 9, p = 0.414). Nested PCR revealed several species of trypanosomes: T. vivax (6.62%), T. congolense (2.57%), and T. brucei and T. simiae each at 0.73%. Blood meal analyses revealed five principal vertebrate hosts, namely, cattle (Bos taurus), humans (Homo sapiens), Nile monitor lizard (Varanus niloticus), African mud turtle (Pelusio schapini) and the African Savanna elephant (Loxodonta africana).Conclusion: We found a moderately high infection rate of 10.78%, with all infections attributed to trypanosome species that are causative agents for the animal disease only. However, more validation using large-scale passive and active screening of human and tsetse samples should be done. Cattle and humans appear to be the most important tsetse hosts in the region and should be considered in the design of interventions.

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Apparent Density, Trypanosome Infection Rates and Host Preference of Tsetse Flies in the Sleeping Sickness Endemic Focus of North-Western Uganda

10.21203/rs.3.rs-43888/v1 ◽

2020 ◽

Author(s):

Robert Opiro ◽

Robert Opoke ◽

Harriet Angwech ◽

Esther Nakafu ◽

Francis A. Oloya ◽

...

Keyword(s):

Infection Rate ◽

Apparent Density ◽

Blood Meal ◽

Nested Pcr ◽

Tsetse Fly ◽

Tsetse Flies ◽

Trypanosome Species ◽

Trypanosome Infection ◽

Infection Rates ◽

Monitor Lizard

Abstract Background: African trypanosomiasis, caused by protozoa of the genus Trypanosoma and transmitted by the tsetse fly, is a serious parasitic disease of humans and animals. Reliable data on the vector distribution, feeding preference and the trypanosome species they carry is pertinent to planning sustainable control strategies.Methodology: We deployed 109 biconical traps in 10 villages in two districts of northwestern Uganda to obtain information on the apparent density, trypanosome infection rates and blood meal sources of tsetse flies. A subset of the collected samples was analyzed for detection of trypanosomes species and sub-species using a nested PCR protocol based on primers amplifying the Internal Transcribed Spacer (ITS) region of ribosomal DNA. 34 blood-engorged adult tsetse midguts were analyzed for blood meal sources by sequencing of the mitochondrial cytochrome c oxidase 1 (COI) and cytochrome b (cytb) genes. Results: Out of the 109 traps deployed, we captured 622 Glossina fuscipes fuscipes tsetse flies (269 males and 353 females). Apparent density (AD) ranged from 0.6 to 3.7 flies/trap/day in the two districts. 29 (10.7%) of the flies were infected with one or more trypanosome species, with infection rate significantly associated with age group (χ2 = 29.733, df = 2, p < 0.05) but not with sex (χ2 = 0.43, df = 1, p = 0.835) and district of origin (χ2 = 1.374, df = 1, p = 0.241). Nested PCR revealed several species of trypanosomes: T. vivax (62.1%), T. congolense (24.14 %), and T. brucei and T. simiae each at 6.89%. Blood meal analyses revealed five principal vertebrate hosts, namely, cattle (Bos taurus), humans (Homo sapiens), Nile monitor lizard (Varanus niloticus), African mud turtle (Pelusio schapini) and the African Savanna elephant (Loxodonta africana).Conclusion: We found a moderately high infection rate at 10.78%, with all infections attributed to trypanosome species that are causative agents for the animal disease only. However, more validation using large-scale passive and active screening of human and tsetse samples should be done. Cattle and humans appear to be the most important tsetse hosts in the region and should be considered in the design of interventions.

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Apparent density, trypanosome infection rates and host preference of tsetse flies in the sleeping sickness endemic focus of Northwestern Uganda

10.21203/rs.3.rs-43888/v4 ◽

2020 ◽

Author(s):

Robert Opiro ◽

Robert Opoke ◽

Harriet Angwech ◽

Esther Nakafu ◽

Francis A. Oloya ◽

...

Keyword(s):

Infection Rate ◽

Apparent Density ◽

Blood Meal ◽

Nested Pcr ◽

Tsetse Fly ◽

Tsetse Flies ◽

Trypanosome Species ◽

Trypanosome Infection ◽

Infection Rates ◽

Monitor Lizard

Abstract Background: African trypanosomiasis, caused by protozoa of the genus Trypanosoma and transmitted by the tsetse fly, is a serious parasitic disease of humans and animals. Reliable data on the vector distribution, feeding preference and the trypanosome species they carry is pertinent to planning sustainable control strategies.Methodology: We deployed 109 biconical traps in 10 villages in two districts of northwestern Uganda to obtain information on the apparent density, trypanosome infection rates and blood meal sources of tsetse flies. A subset (272) of the collected samples was analyzed for detection of trypanosomes species and sub-species using a nested PCR protocol based on primers amplifying the Internal Transcribed Spacer (ITS) region of ribosomal DNA. 34 blood-engorged adult tsetse midguts were analyzed for blood meal sources by sequencing of the mitochondrial cytochrome c oxidase 1 (COI) and cytochrome b (cytb) genes. Results: Out of the 109 traps deployed, we captured 622 Glossina fuscipes fuscipes tsetse flies (269 males and 353 females). Apparent density (AD) ranged from 0.6 to 3.7 flies/trap/day in the two districts. 29 (10.7%) of the flies were infected with one or more trypanosome species. Infection rate was not significantly associated with age group (χ2 = 5.001, df=2, p = 0.082), sex of the fly (χ2 = 0.099, df = 1, p = 0.753), district of origin (χ2= 0.629, df = 1, p = 0.428) and village of origin (χ2= 9.252, df = 9, p = 0.414). Nested PCR revealed several species of trypanosomes: T. vivax (6.62%), T. congolense (2.57%), T. brucei and T. simiae each at 0.73%. Blood meal analyses revealed five principal vertebrate hosts, namely, cattle (Bos taurus), humans (Homo sapiens), Nile monitor lizard (Varanus niloticus), African mud turtle (Pelusio schapini) and the African Savanna elephant (Loxodonta africana).Conclusion: We found an infection rate of 10.78 %, with all infections attributed to trypanosome species that are causative agents for the animal disease only. However, more verification of this finding using large-scale passive and active screening of human and tsetse samples should be done. Cattle and humans appear to be the most important tsetse hosts in the region and should be considered in the design of interventions.

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P104 One year failure rates for de novo ventriculo-peritonealshunts in under 3- month-old children

Journal of Neurology Neurosurgery & Psychiatry ◽

10.1136/jnnp-2019-abn.161 ◽

2019 ◽

Vol 90 (3) ◽

pp. e50.1-e50

Author(s):

E Bentley ◽

R Ved ◽

A Amato-Watkins ◽

J Lang ◽

G Zilani ◽

...

Keyword(s):

Infection Rate ◽

De Novo ◽

Descriptive Statistics ◽

Infection Rates ◽

Older Children ◽

Single Centre ◽

Single Centre Study ◽

One Year ◽

Shunt Survival ◽

Shunt Infections

ObjectivesHistorically VPS failure and infection rates are higher for neonates than for older children. We compared our one year VPS failure and infection rates in under 3-month-olds with those of older children.DesignA retrospective, single centre study comparing 1 year survival and infection rates of VPS in under 3-month-olds verses older children.Subjects58 children under 3 months of age underwent VPS insertion between January 2007 and December 2016.MethodsData was collected by three independent reviewers from electronic files and case notes. Data was analysed using descriptive statistics and one year shunt survival curves were produced.ResultsFor children under 3 months there was a 29.3% one-year shunt failure rate, of which 2 were shunt infections (3.4%). In patients greater than 3 months, the shunt malfunction rate was 23.4% and the infection rate was 4.3%. There were no shunt-related mortalities in either group.ConclusionsChildren under 3-months-old undergoing VPS insertion should not automatically expect an increased 1 year failure or infection rate compared with older children. Reasons for this may be increased sub-specialisation, improved neonatal care and use of antibiotic impregnated catheters.

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First report of detection of Toxoplasma gondii DNA in oysters (Crassostrea sp.) in the state of Maranhão

Revista Brasileira de Parasitologia Veterinária ◽

10.1590/s1984-29612020050 ◽

2020 ◽

Vol 29 (3) ◽

Cited By ~ 1

Author(s):

Camila Moraes Silva ◽

Anna Letícia Pinto Silva ◽

Karinne Francisca Cardoso Watanabe ◽

Nancyleni Pinto Chaves Bezerra ◽

Danilo Cutrim Bezerra ◽

...

Keyword(s):

Toxoplasma Gondii ◽

Dna Extraction ◽

Nested Pcr ◽

The State ◽

Molecular Technique ◽

Visceral Mass ◽

First Report ◽

Potential Sources ◽

Sources Of Contamination ◽

Commercial Kit

Abstract The aim of this study was to report on detection of Toxoplasma gondii DNA in oysters (Crassostrea sp.) in the state of Maranhão. To conduct this study, 200 farmed oysters were acquired in the municipality of Raposa and 100 in Paço do Lumiar; and a further 100 oysters were taken from the natural stock in the municipality of Primeira Cruz. This total of 400 specimens sampled was divided into 80 pools composed of five animals each. The gills and visceral mass of each oyster were removed for DNA extraction (per pool of oysters), using a commercial kit. The nested PCR technique (with the primer SAG-1) was then used to investigate any presence of protozoa. This molecular technique demonstrated the presence of DNA of T. gondii in 2.5% of the pools of oysters (n = 2/80): these oysters were exclusively from farms. The results from this study allow the conclusion that oysters of the genus Crassostrea that are farmed in the state of Maranhão are capable of filtering oocysts of T. gondii and maintaining them in their tissues. They are therefore potential sources of contamination for humans and other animals.

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PCR-positivity of gerbils and their ectoparasites for Leishmania spp. in a hyperendemic focus of zoonotic cutaneous leishmaniasis in central Iran

10.21203/rs.2.21837/v1 ◽

2020 ◽

Author(s):

Sahar Azarmi ◽

Alireza Zahraei-Ramazani ◽

Mehdi Mohebali ◽

Yavar Rassi ◽

Amir Ahmad Akhavan ◽

...

Keyword(s):

Cutaneous Leishmaniasis ◽

Infection Rate ◽

Microscopic Examination ◽

Nested Pcr ◽

Central Iran ◽

Nested Polymerase Chain Reaction ◽

Zoonotic Cutaneous Leishmaniasis ◽

Leishmania Spp ◽

Different Seasons

Abstract Background: Sand flies are the only known vectors of Leishmania parasites. Various arthropods, including ticks have been suggested as secondary vectors of Leishmania spp. many years ago. This study was conducted to determine PCR-positivity of zoonotic cutaneous leishmaniasis reservoir hosts and their ectoparasites for Leishmania spp. in central Iran. Methods: Microscopic examination and nested polymerase chain reaction (Nested-PCR) were used to detect and identify species of Leishmania and the results were confirmed by two methods, PCR-restriction fragment length polymorphism (PCR-RFLP) and sequencing. Results: Totally, 93 rodents (Rhomombis opimus (n=92) and Nesokia indica (n=1)) were captured during different seasons and 9 different species of ectoparasites were collected from them. Out of 92 collected R. opimus, 14 were positive for Leishmania spp. by microscopic examination while one N. indica and 77 R. opimus were positive by nested-PCR. The infection rate of rodents with Leishmania major and Leishmania turanica was 39.79% and 15.05%, respectively. Mixed natural infections with L. major and L. turanica were seen in 15.05% of rodents, in 7.53% of the rodents with L. major and Leishmania gerbilli, and in 6.45% of the rodents with the three species. The leishmanial infection rate of the rodents was the highest (94.29%) in summer and lowest (45.45%) in the winter. Moreover, 39 out of 54 fleas, 5 out of 8 mites, and 1 tick were PCR positive for Leishmania parasites. Conclusions: The highest rate of infection with L. major and L. turanica in R. opimus populations was observed in the summer and spring respectively, and the highest percentage of L. major and L. turanica coinfection was seen in the winter. It is suggested that the role of L. turanica and the probable role of ectoparasites in the transmission of epidemiology should be investigated carefully. Xenodiagnostic testing is recommended for future testing.

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Toxoplasma gondii in sheep and goat livers: Risks for human consumption

Journal of the Hellenic Veterinary Medical Society ◽

10.12681/jhvms.20344 ◽

2019 ◽

Vol 70 (1) ◽

pp. 1387 ◽

Cited By ~ 2

Author(s):

S. BAHRAMI ◽

M. ZAREI ◽

M. GHORBANPOUR ◽

S. KARAMI

Keyword(s):

Toxoplasma Gondii ◽

Animal Species ◽

Human Infection ◽

Zoonotic Diseases ◽

Enzyme Linked Immunosorbent Assay ◽

Human Consumption ◽

Sheep And Goats ◽

Baseline Information ◽

Polymerase Chain ◽

Undercooked Meat

Toxoplasmosis is one of the most important zoonotic diseases worldwide and is caused by the protozoan Toxoplasma gondii. Besides vertical transmission during pregnancy, humans can become infected post-natally either by oral uptake of sporulated Toxoplasma oocysts or through ingestion of tissue cysts upon consumption of raw or undercooked meat. The aim of this study was to approximate the risk of human infection via liver consumption by estimating the seroprevalence and molecular prevalence of T. gondii in slaughtered sheep and goats in Iran. In the present study, livers from 150 sheep and 150 goats were collected at slaughter. In- house enzyme-linked immunosorbent assay was performed in T. gondii liver juice. Parasite-specific polymerase chain reaction was carried out on all samples obtained from liver tissues. Antibodies against T. gondii were detected by in-house ELISA in 32.6% sheep and 48% goat livers and 8% and 11.3% of sheep and goat livers were positive for the presence of T. gondii DNA, respectively. The results of this study provide baseline information on the presence of T. gondii in sheep and goats livers and imply an important human health and hygienic risk associated with the consumption of raw or undercooked liver from these animal species.

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