Научная статья на тему 'Endoparasic diseases of ostriches in eastern Ukraine'

Endoparasic diseases of ostriches in eastern Ukraine Текст научной статьи по специальности «Биологические науки»

CC BY
237
60
i Надоели баннеры? Вы всегда можете отключить рекламу.
Журнал
Ukrainian Journal of Ecology
Область наук
Ключевые слова
ostriches / helminths / Eimeria / nematodes / eggs / invasion

Аннотация научной статьи по биологическим наукам, автор научной работы — A.P. Paliy, N.V. Sumakova, R.V. Petrov, A.V. Berezovskiy, V.I. Risovaniy

In ostrich farming is difficult to obtain the necessary production and economic results without protection of bird health. We determined the incidence of parasitic ostriches during the period of growing and keeping on specialized eco-zoos. Samples from small and large farms, as well as eco-parks in Kharkiv, Dnepr and Donetsk regions of Ukraine, were examined during 2016-2020. We performed a parasitological study of 159 samples from three species of ostriches (black African ostrich, Australian common Emu (Dromaius), Rhea). Infestation of ostriches of different ages with two types of nematodes and Eimeria was established. We determoined that the population of ostriches in specialized farms and eco-zoos was infested with nematodes and protozoa with an extensiveness of invasion from 7.7% to 71.4% among adult birds, while young ostriches were infested with Emeria from 20.0% to 44.4%. The largest invasion by helminths and protozoa was observed among black African ostriches in Kharkiv region (41.4%), in Dnepr region it was 33.3%, and in Donetsk it reached 34.1%. Among the livestock of ostriches, there were both mono and mixinvasions. Most often, this was an invasion by Trichostrongylus spp. and Eimeria spp. in African black ostriches, capillaries and Eimeria in Emu. In Kharkiv region, the invasion of Capillaria by Trichostrongylus in African ostriches and Trichostrongylus in Emu were found when they were kept together. Acute and chronic eimeriosis disease can lead to the death of ostriches at the age of 3-4 months.

i Надоели баннеры? Вы всегда можете отключить рекламу.
iНе можете найти то, что вам нужно? Попробуйте сервис подбора литературы.
i Надоели баннеры? Вы всегда можете отключить рекламу.

Текст научной работы на тему «Endoparasic diseases of ostriches in eastern Ukraine»

Ukrainian Journal of Ecology

Ukrainian Journal ofEcology, 2020, 10(4), 235-241, doi: 10.15421/2020_193

ORIGINAL ARTICLE UDC619:616.995.1:568.221(477)

Endoparasic diseases of ostriches in eastern Ukraine

A.P. Paliy1, N.V. Sumakova1, R.V. Petrov2, A.V. Berezovskiy2, V.I. Risovaniy2, G.A. Zon2, L.B. Ivanovskaya2, A.I. Fotin2, R.V. Dolbanosova2, L.P. Livoshchenko2, Ye.M. Livoshchenko2,

A.P. Palii3

1 National Scientific Center Institute of Experimental and Clinical Veterinary Medicine, 83, Pushkinska St, Kharkiv, 61023, Ukraine 2Sumy National Agrarian University, 160, Herasym Kondratiev St, Sumy, 40021, Ukraine 3 Kharkiv National Technical University of Agriculture named after Petro Vasylenko, 44, Alchevskih St, Kharkiv, 61002, Ukraine Corresponding author E-mail: paliy. dok@gmail. com Received: 11.08.2020. Accepted27.09.2020

In ostrich farming is difficult to obtain the necessary production and economic results without protection of bird health. We determined the incidence of parasitic ostriches during the period of growing and keeping on specialized eco-zoos. Samples from small and large farms, as well as eco-parks in Kharkiv, Dnepr and Donetsk regions of Ukraine, were examined during 20162020. We performed a parasitological study of 159 samples from three species of ostriches (black African ostrich, Australian common Emu (Dromaius), Rhea). Infestation of ostriches of different ages with two types of nematodes and Eimeria was established. We determoined that the population of ostriches in specialized farms and eco-zoos was infested with nematodes and protozoa with an extensiveness of invasion from 7.7% to 71.4% among adult birds, while young ostriches were infested with Emeria from 20.0% to 44.4%. The largest invasion by helminths and protozoa was observed among black African ostriches in Kharkiv region (41.4%), in Dnepr region it was 33.3%, and in Donetsk it reached 34.1%. Among the livestock of ostriches, there were both mono and mixinvasions. Most often, this was an invasion by Trichostrongylus spp. and Eimeria spp. in African black ostriches, capillaries and Eimeria in Emu. In Kharkiv region, the invasion of Capillaria by Trichostrongylus in African ostriches and Trichostrongylus in Emu were found when they were kept together. Acute and chronic eimeriosis disease can lead to the death of ostriches at the age of 3-4 months.

Key words: ostriches, helminths, Eimeria, nematodes, eggs, invasion.

Introduction

Ostrich farms bring their owners a steady income in more than a hundred countries around the world. Ostriches are a prolific but not whimsical bird, almost entirely recyclable. They belong to long-livers (life expectancy reaches 70 years), and the mature age lasts up to 30-40 years. In organizing a business, such areas as commercial (obtaining meat, eggs, skin, feathers, fat, etc.), breeding (selling juveniles) and agritourism are possible (Ross & Deeming, 1998; Cloete et al., 2008; Magige et al., 2009; Menon et al., 2014). Farmer breeding of ostriches originated in South Africa about 150 years ago. In 1885, the number of domesticated birds in South Africa did not exceed 80 birds. The birds were bred primarily to meet the demand for ostrich feathers. Today, there are 350 farms in this country, which contain more than 90 thousand ostriches, which produce about 30.000 kg of feathers annually (Boum & Bonine, 2015; Magige & R0skaft, 2017). Over time, ostrich farms began to be created in Australia, Egypt, USA, Argentina. In the 70s of the last century, the emphasis gradually shifted to the production of poultry meat and skins. Even 15 years ago, the ostrich population numbered no more than a few thousand, now about three and a half million ostriches are raised on farms in 130 countries. On 12.000 farms in the United States, about 100.000 adults are kept (Bejaei & Chengb 2014). In Mexico, the first ostrich farm was established in 1988 and the sale of breeding stock was profitable until 2008. Until 201 6, about 30 farms remained active (Moreno & Rendon, 2020).

In Europe, Italy and Spain are the leaders in the number of these birds. Poland is the most successful example of ostrich breeding in Europe: about 200 farms have been established there in the last decade alone (Horbanczuk et al., 2008). There has been an increase in interest in raising ostriches in China (Feng et al., 2017). The real ostrich boom began in the late 1980s, when studies of American scientists recommending a healthy lifestyle showed that ostrich meat contains one and a half times less cholesterol and nine times less fat than, for example, beef, not inferior to the latter in taste (Al-Khalifa & Al-Naser, 2014; Horbanczuk et al., 2019).

Ostrich farming is a relatively young poultry industry in Ukraine. Today about 60 farms are engaged in raising ostriches. Despite the fact that the first farms that work in this direction appeared in the early 2000, this business is still considered new and exotic

(Polishchuk et al., 2020). The economic interest in breeding ostriches in Ukraine is due to the opportunity to obtain high-quality products in a short time.

African ostriches were brought to the Ukrainian steppes by Baron Friedrich Edward Falz-Fein as an experiment and took root in the Askania-Nova estate. In the Crimea in 1913 there were about 300 ostrich farms. In recent years, ostrich farms have been created in Kiev, Dnepropetrovsk, Lugansk, Kherson, as well as in Poltava, Sumy and Kharkiv regions. The most popular in farming and specialized poultry farms are African ostriches and Australian ostriches. It is these species of running or, so-called, keel-free birds that have high adaptive qualities and performance levels, and adapt more quickly to technological processes (Strashnyuk & Kiritchenko, 2014). Growing ostriches makes it possible to obtain a variety of products in a short period of time - juveniles, adult birds, hatching and food eggs, slaughter and processing products, down, feathers, etc. (Brand et al., 2018; Cooper, 2000). All ostrich species have high adaptive properties; the survival rate of young and adult birds is at the level of 7585% (Zhang et al., 2017).

Now conditions have been created for the import of live ostriches from Europe, Africa and Australia. This is a direct threat of the emergence of new, unknown to us infectious and invasive diseases and their spread in safe areas (Springborn et al., 2015). Scientific knowledge about ostrich diseases is incomplete and very fragmented, and specific details on the technical aspects of diagnostic and screening tests are in most cases completely lacking (Verwoerd, 2000; Kritas, 2001). Since ostriches are a species unusual for the territory of Ukraine, they historically live in other climatic conditions, the diseases inherent in these birds in Ukraine are poorly studied. For successful breeding of ostriches, first of all, it is necessary to have sufficient knowledge about their vital activity. Only then is it possible to reduce the risk of their morbidity to a minimum. The key to success in this area is three factors: a complex of veterinary preventive measures, a high-quality feed base, strict adherence to the technological process (Ipek & Sahan, 2004). One of the most common problems in captive breeding of ostriches is the fight against parasitic diseases (Ederli & de Oliveira, 2014; da Silva & Langoni, 2016; Feng et al., 2017). Therefore, the study of the characteristics of parasitic diseases of ostriches in Ukraine is a necessary strategy for maintaining the health of birds and obtaining safe products.

Materials and methods

The aim of our work was to study the main endoparasitic diseases of ostriches in different regions of Ukraine. The experiments were carried out in the laboratory of veterinary sanitation and parasitology of the National Scientific Center "Institute of Experimental and Clinical Veterinary Medicine" (Kharkiv). During 2016-2020, monitoring of invasive diseases of ostriches was carried out on farms for their cultivation in various regions of Ukraine (Donetsk, Kharkiv, Dniprovsk regions). The objects of research were ostriches of different age groups. A clinical examination of black African ostriches (Struthio camelus Linnaeus, 1758), Australian common Emu (Dromaius novaehollandiae Latham, 1790) and rhea (Rhea americana Linnaeus, 1758) was carried out according to existing methods (Yuksek et al., 2002; Buergelt, 2020). Helminoproscopic studies of fecal samples from ostriches of different age groups were carried out using the method of direct smear and concentration (flotation and sedimentation) (Tomza-Marciniak et al., 2014; Byrnea et al., 2018; Ola-Fadunsin et al., 2019). The extent of bird invasion was determined by the formula:

El = x/yx100

where: El - extent invasion, x- the number of animals that have identified eggs or larvae of helminths, y - total number of animals examined, 100 - percentage conversion factor.

Parasitological autopsies of ostriches were carried out according to Wang et al. (2017).

Results

During a clinical examination of adult African ostriches, some observed depression, inactivity, decreased appetite, growth retardation, weight loss, dysfunction of the gastrointestinal tract. Conducted coproovoscopic studies were identified eggs of nematodes and oocysts of the Eimeria spp. (Table 1).

Consequently, the adult population of ostriches in specialized and private farms, in eco-zoos is infested with nematodes and protozoa with an extensiveness of invasion from 38.1% to 71.4%. Along with this, young ostriches are infested with Eimeria from 18.2.0% to 44.4%. The greatest infection with helminths and protozoa is observed among black African ostriches in the Kharkiv region - 41.2%, in the Dnepr region it was the least - 33.3%, and in the Donetsk region it reached 34.1%. Parasite infestation in ostriches is most often manifested by general depression, inactivity, decreased appetite, growth and development retardation, and gastrointestinal upset.

Taking into account the data presented by other researchers (Ederli & de Oliveira, 2014), we differentiated helminth eggs isolated from ostriches from different regions of Ukraine (Table 2).

We made a parasitological dissection of two corpses of 3 and 4-month ostriches. The first ostrich cub died at the age of 3 months in a farm in the Kharkiv region in September 2016 with signs of a disorder of the gastrointestinal tract, with suspicion of the presence of a foreign body in the intestine. During dissection revealed: fibrinous layers on the liver, discoloration of its individual areas; hyperemia and edema of the intestinal mucosa, liquid contents of the intestine; thickening of the walls of the cecum with hemorrhages on the mucous membrane. The contents of the intestines are bloody with an unpleasant odor; microscopic examination of smears of prints and flotation examination of the contents of the cecum revealed oocysts of Eimeria from 85 to 125 pieces in the field of view of the microscope. Oocysts of Imperia are also found in the contents of the rectum. There were no foreign bodies in the stomach and intestines. We have been diagnosed with acute edgy - eimeriosis.

237 Endoparasic disease of ostriches

Table 1. Extensiveness of invasion among ostriches in Ukraine

Species Bird age Number of samples Number of positive samples Extent invasion, % Parasite species

Dniprovsk (Dnepr) region

Black African ostrich > 3 years 21 8 38.1 Nematodae spp.

(Struthio camelus) Eimeria spp.

2 months 6 - - -

4 months. 9 4 44.4 Eimeria spp.

9 months 12 4 33.3 Eimeria spp.

Summary 48 16 33.3 -

Australian common > 3 years 5 2 40.0 Nematodae spp.

Emu (Dromaius Eimeria spp.

novaehollandiae)

Nandu(Rhea > 3 years 2 - - -

americana)

Total 55 18 32.7 -

Donetsk region

Black African ostrich > 3 years 30 12 40.0 Nematodae spp.

(Struthio camelus) Eimeria spp.

3 months 11 2 18.2 Eimeria spp.

Summary 41 14 34.1 -

Australian common > 3 years 8 1 12.5 Nematodae spp.

Emu (Dromaius 3 months 5 - - -

novaehollandiae)

Summary 13 1 7.7 -

Total 54 15 27.8 -

Kharkov region

Black African ostrich > 3 years 7 5 71.4 Nematodae spp.

(Struthhio camelus) 3 months 10 2 20.0 Eimeria spp.

Summary 17 7 41.2 -

Australian common > 3 years 9 2 22.2 Nematodae spp.

Emu (Dromaius Eimeria spp.

novaehollandiae) 9 months 9 2 22.2 Eimeria spp.

Summary 18 4 22.2 -

Nandu(Rhea > 4 years 5 1 20.0 Nematodae spp.

americana) 3 months 10 4 40.0 Eimeria spp.

Summary 15 5 33.3 -

Total 50 16 32.0 -

Table 2. Ostrich endoparasites fauna in Ukraine

Species Number of positive samples Parasite species

Dnepr region

Black African ostrich 3 Ca pill aria spp.

(Struthio camelus) 2 Libyostrongylus douglassii

1 Libyostrongylus douglassii, Eimeria spp.

8 Eimeria spp.

Australian common Emu 1 Capillaria spp. Eimeria spp.

(Dromaius novaehollandiae) 1 Libyostrongylus douglassii

Donetsk region

Black African ostrich 2 Capillaria spp.

(Struthio camelus) 8 Libyostrongylus douglassii

2 Libyostrongylus douglassii, Eimeria spp.

2 Eimeria spp.

Australian common Emu 1 Capillaria spp., Eimeria spp.

(Dromaius novaehollandiae)

Kharkiv region

Black African ostrich 1 Capillaria spp.

(Struthio camelus) 3 Libyostrongylus douglassii

1 Capillaria spp., Libyostrongylus douglassii

2 Eimeria spp.

Australian common Emu 1 Libyostrongylus douglassii

(Dromaius novaehollandiae) 1 Capillaria spp., Eimeria spp.

2 Eimeria spp.

Nandu (Rhea americana) 1 Capillaria spp.

4 Eimeria spp.

In second case, the ostrich died at the age of 4 months at the zoo in 2017. The chick was ill for a week, refused food, he was prescribed antibiotics. During the autopsy of the corpse found: enlargement of the liver, change of color of its individual areas, blood filling of parenchima, stomach half-empty, covered with mucus, walls of blind intestines thickened, in the lumen available layers of fibrin. The large intestine is inflamed with hemorrhage, the contents with a slight touch of blood. In microscopic examination of the contents of the blind intestines and large intestines revealed oocysts of Eimeria from 65 to 85 pieces in the field of view of the microscope, (the final diagnosis - chronic eimeriosis). So, acute and chronic eimeriosis can lead to the death of young animals at the age of 3-4 months. This, in turn, leads to significant economic losses.

We have proved that both mono (27.0%) and mixed (4.4%) ostriches are found among the invazition. African black ostriches are most common infestation by Trichostrongylus and Eimeria, and Dromaius - Capiyaria and Eimeria. It should be noted that in the Kharkiv region, Trichostrongylus invaction was found in African ostriches and Dromaius, which were kept in the same enclosure. Ostriches were infested with Eimeria with an invasion rate of 25.0%.

Discussion

The problem of parasitic diseases of agricultural and domestic animals remains relevant today (Paliy et al., 2018a; 2018b; 2018c; 2019), despite the introduction of new high-performance anthelminths (Lloyd et al., 2000; Lambertz et al., 2019; Preston et al., 2019) and disinfectants (Paliy et al., 2015; 2016; 2020a; Stegniy et al., 2019; Bondarchuk et al., 2019).

Most recently, the results of advanced studies of ostrich parasites (Struthio camelus), mainly from European countries where commercial ostrich farming is gaining momentum (Cooper, 2005) have been published. Parasitological studies are important for the conservation of livestock, as they allow us to assess the risk of transmission of pathogens to ostriches born in captivity from imported wild populations and vice versa (Rafael et al., 2013). The results we received are different from the previous results of 2010. At that time, adult African ostriches from the Donetsk region farm were found to be 100% infected with nematodes of two types of the Strongylata contract. Ostriches 2-3 months of age were 10% invasive, and Emu ostriches were invasive (Babenko et al., 2010).

Infection with nematodes of African ostriches today is 34.1% in the Donetsk region, 6.3% of ostriches affected by Capilaria, 27.8% - Tihostrengylus one species Libyososgytronlus douglassii. In addition, among the adult livestock there was invasive Eimeria, which was 2.1 %. The infestation of the Eimeria among ostriches reaches 29.6%, which is 2.9 times higher than before. The results obtained in the Dnepr region are also different from those of other researchers (Marshalkina et al., 2013). At that time, the invasiveness of ostriches with Ascarids, Capyllaria and Ttrihostrengylus with EI from 6% to 60% was recorded. According to our results, the invasiveness of ostriches of all species was 32.7%, and the most invasive adult African ostriches by nematodes is 38.1% (14.2% - capillaries, 19.0% - Libyostrongylus douglassii, 5.2% - Libyostrongylus douglassii, Eimeria spp., emu ostriches - 40.0% (20.0% - capillaries, 20% - Libyostrongylus douglassii). The infestation of Ascaridia ostriches was not detected, which indicates that the parasitofauna of ostriches in Ukraine is changing and needs more research. Other researchers note a low level of damage to ostriches by nematodes (Cooper, 2005). There are mixed infestations in the zoo bird (Papini et al., 2012).

Libyostrongylus douglassii nematodes of the genus Libyostrongylus - hematophagi-parasites that find themselves under the membrane of the forearms of the ostrich: they are common and can cause 50% of the death of young, and sometimes death of adults (Nemejc & Lukesova, 2012). This species has been found in ostriches from Africa, Europe, the Americas and Oceania (de Souza et al., 2019), although the natural range of ostriches is Africa (Barton & Seward, 1993). In our studies among the invasive population of African ostriches EI reaches 45.9%, in it - 20.0%, and in the nandu of this pathogen we did not show. Other researchers report the invasiveness of ostriches (Kritas, 2001; Rafael et al., 2013), and in our results we note the presence of these pathogens in all species of ostriches in three regions of Ukraine. Infestation is common in many countries of the world, where ostriches are grown (Khatri & Maharjan, 2018), but it varies from 0.6 to 60%, and according to our research it is 15.3% among adult birds, and 26.5% among young people. The disease of acute and chronic eimeriosis leads to the death of ostrich at the age of 3-4 months.

The presence of helminths we have identified in ostriches is confirmed by other researchers (Ponce Gordo et al., 2002; Ederli & de Oliveira, 2015; Gallo et al., 2020). Analysis of the invasiveness of ostriches, showed that gradually changes parasstophauna pathogens helminths. It differs from the parasitophauna that is inherent in ostriches in their historical homeland and in Europe (Sotiraki et al., 2001). Most foreign studies are devoted to the study of nematodes from the genus Libyostrongylus, and in our case we need to study more representatives of the genus Capillaria, the invasive of which in our conditions reaches 27.8%. The infestation of juveniles of all kinds is also a pressing problem of modern times. She grew many times, and the appearance of infestation among adult birds indicates that the pathogen remained in the body of birds, which have already grown in the farms of Ukraine. This means that the quarantine measures that are carried out in farms when importing poultry - substandard. A great deal of attention should be paid to the set of veterinary and sanitary measures, which are mandatory in the breeding and cultivation of farm animals and poultry (Zavgorodniy et al., 2013; Paliy et al., 2020b).

Conclusions

Adult ostriches (over 3 years old) in specialized and farms, in eco-zoos of Kharkiv, Donetsk and Dnepr regions of Ukraine are invasive nematodes and protozoa with the extensiveity of invasion from 38.1% to 71.4% among adult birds. Among ostriches of all species aged 3 to 9 months, the infestation of the inmates ranges from 18.2% to 44.4%. Among black African ostriches in Kharkiv region, inhibition of helminths and protozoa is 41.2%, in Dnepr it is the smallest - 33.3%, and in Donetsk it is 34.1 %. Among the number of ostriches there are both mono (27.0%) and mixinazia (4.4%). African black ostriches are more often infected with Trihostrengylus and Eimeria, Dromaius - Capylaria and Eimeria.

239 Endoparasic disease of ostriches

iНе можете найти то, что вам нужно? Попробуйте сервис подбора литературы.

Among the livestock of ostriches, there are both mono (27.0%) and mixinvasions (4.4%). Most often, this is the invasived of Trichostrongylus and Eimeria in African black ostriches, Capilaria and Eimeria in Dromaius. In rhea, mono invasived of Capillaria was found in adult birds. In the Kharkiv region, an invasivtd of Capillaria with Trichostrongylus in African ostriches and Trichostrongylus in Dromaius, which were kept in the same enclosure. The disease of acute and chronic eimeriosis can lead to the death of juveniles at the age of 3-4 months. To prevent the infected of ostriches, during the importation of a new batch of poultry, quarantine must be at least four weeks. It is mandatory to conduct parasitic studies and a set of veterinary and sanitary measures.

References

Al-Khalifa, H., & Al-Naser, A. (2014). Ostrich meat: Production, quality parameters, and nutritional comparison to other types of

meats. Journal of Applied Poultry Research, 23(4), 784-790. doi: 10.3382/japr.2014-00962 Babenko, A. B., Lucenko, L. I., & Sumakova, N. V. (2010). Parazytarni zakhvoryuvannya strausiv [Parasitic diseases of ostriches].

Veterinary Medicine, 93, 22-24. (in Ukrainian) Barton, N. J., & Seward, D. A. (1993). Detection of Libyostrongylus douglassi in ostriches in Australia. Australian Veterinary

Journal, 70(1), 31 -32. doi: 10.1111 /j.1751 -0813.1993.tb00796.x Bejaei, M., & Cheng, K. M. (2014). A survey of current ostrich handling and transport practices in North America with reference to ostrich welfare and transportation guidelines set up in other countries. Poultry Science, 93(2), 296-306. doi: 10.3382/ps.2013-03417

Bondarchuk, A. O., Paliy, A. P., & Blazheyevskiy, M. Ye. (2019). Determination of acute toxicity of the «Bondarmin» disinfectant.

Journal for Veterinary Medicine, Biotechnology and Biosafety, 5(2), 26-30. doi: 10.36016/JVMBBS-2019-5-2-5 Boum, A., & Bonine, M. (2015). The elegant plume: ostrich feathers, African commercial networks, and European capitalism. The

Journal of North African Studies, 20(1), 5-26. doi: 10.1080/13629387.2014.983733 Brand, T. S., Kritzinger, W. J., Van der Merwe, D. A., Muller, A., Hoffman, L. C., & Niemann, G. J. (2018). Feather and skin development of ostriches Struthio camelus. Journal of the South African Veterinary Association, 89(0), e1-e5. doi:10.4102/jsava.v89i0.1556

Buergelt, C. D. (2020). Diseases of Ostriches and Other Ratites. Journal of Wildlife Diseases, 36(3), 599. doi: 10.7589/0090-355836.3.599

Byrnea, R. L., Fogartyb, U., Mooneya, A., Marples, N. M., & Hollanda, C. V. (2018). A comparison of helminth infections as assessed through coprological analysis and adult worm burde ns in a wild host. IJP: Parasites and Wildlife, 7(2018), 439-444. doi: 10.1016/j.ijppaw.2018.11.003

Cloete, S. W. P., Engelbrecht, A., Olivier, J. J., & Bunter, K. L. (2008). Deriving a preliminary breeding objective for commercial

ostriches: an overview. Australian Journal of Experimental agriculture, 48(10), 1247-1256. doi: 10.1071/ea08135 Cooper, R. G. (2005). Bacterial, fungal and parasitic infections in the ostrich (Struthio camelusvar. domesticus). Animal Science

Journal, 76(2), 97-106. doi: 10.1111 /j.1740-0929.2005.00243.x Cooper, R. G. (2000). Management of ostrich (Struthio camelus) chicks. World's Poultry Science Journal, 56(1), 33-44. doi: 10.1079/WPS20000004

da Silva, R. C., & Langoni, H. (2016). Risk factors and molecular typing of Toxoplasma gondii isolated from ostriches (Struthio

camelus) from a Brazilian slaughterhouse. Veterinary parasitology, 225, 73-80. doi: 10.1016/j.vetpar.2016.06.001 de Souza, L. P., de Andrade, J. G., Medina, R. M., de Carvalho, E. C. Q., Glória, L. S., DaMatta, R. A., & de Paula Santos, C. (2019). Anatomopathological changes, quantification and distribution of Libyostrongylus spp. in regions of the proventriculus and ventriculus of naturally- and experimentally-infected ostriches. Avian Pathology, 48(4), 382-389. doi: 10.1080/03079457.2019.1607254 Ederli, N. B., & de Oliveira, F. C. R. (2014). Comparative morphology of the species of Libyostrongylus and Codiostomum, parasites from ostriches, Struthio camelus, with a identification key to the species. Revista Brasileira de Parasitologia Veterinária, 23(3), 291 -300. doi: 10.1590/S1984-29612014061 Ederli, N. B., & de Oliveira, F. C. R. (2015). Gastrointestinal nematodes in ostriches, Struthio camelus, in different regions of the

state of Rio de Janeiro, Brazil. Braz. J. Vet. Parasitol., Jaboticabal, 24(2), 168-173. doi: 10.1590/S1984-29612015052 Feng, Y., Lu, Y., Wang, Y., Zhang, L., & Yang, Y. (2017). Toxoplasma gondii and Neospora caninum in farm-reared ostriches

(Struthio camelus in China. BMC Veterinary Research, 13, 301. doi: 10.1186/s12917-017-1221 -2 Gallo, S. S. M., Teixeira, C. S., Ederli, N. B., & Oliveira, F. C. R. (2020). Gastrointestinal parasites of a population of emus (Dromaius

novaehollandiae) in Brazil. Brazilian Journal of Biology, 80(1), 66-72. doi: 10.1590/1519-6984.189922 Horbañczuk, J. O., Tomasik, C., & Cooper, R. G. (2008). Ostrich Farming in Poland - Its History and Current Situation after

Accession to the European Union. Avian Biology Research, 1 (2), 65-71. doi: 10.3184/175815508X360470 Horbañczuk, O. K., Moczkowska, M., Marchewka, J., Atanasov, A. G., & Kurek, M. A. (2019). The Composition of Fatty Acids in Ostrich Meat Influenced by the Type of Packaging and Refrigerated Storage. Molecules, 24(22), 4128. doi: 10.3390/molecules24224128

Ipek, A., & Sahan, U. (2004). Effect of breeder age and breeding season on egg production and incubation in farmed ostriches.

British poultry science, 45(5), 643-647. doi: 10.1080/00071660400006339 Khatri, K., & Maharjan, M. (2018). Gastrointestinal parasites of Emu (Dromaius novaehollandiae Latham, 1790) in Ostrich Nepal Pvt. Ltd Gongoliya, Rupandehi, Nepal. Journal of Natural History Museum, 30, 269-273. doi: 10.3126/jnhm.v30i0.27602

Kritas, S. K., (2001). The main medical problems of ostriches. Journal of the Hellenic Veterinary Medical Society, 52(3), 169-175. doi: 10.12681 /jhvms.15421

Lambertz, C., Poulopoulou, I., Wuthijaree, K., & Gauly, M. (2019). Anthelmintic efficacy against gastrointestinal nematodes in goats raised under mountain farming conditions in northern Italy. BMC veterinary research, 15(1), 216. doi: 10.1186/s12917-019-1968-8

Lloyd, S., Smith, J., Connan, R. M., Hatcher, M. A., Hedges, T. R., Humphrey, D. J., & Jones, A. C. (2000). Parasite control methods used by horse owners: factors predisposing to the development of anthelmintic resistance in nematodes. The Veterinary record, 146(17), 487-492. doi: 10.1136/vr.146.17.487 Magige, F. J., Stokke, B. G., Ragna Sortland, R., & R0skaft, E. (2009). Breeding biology of ostriches (Struthio camelus) in the

Serengeti ecosystem, Tanzania. Africa Journal of Ecology, 47(3), 400-408. doi: 10.1111 /j.1365-2028.2008.01002.x Magige, F., & R0skaft, E. (2017). Medicinal and commercial uses of ostrich products in Tanzania. Journal Ethnobiology

Ethnomedicine, 13, 48(2017). doi: 10.1186/s13002-017-0176-5 Marshalkina, T. V., Zaikina, G. V., & Kriva, G. O. (2013). Epizootolohichnyy monitorynh hel'mintoznykh ta protozoynykh khvorob sviys'koyi ptytsi u promyslovykh, fermers'kykh ta prysadybnykh hospodarstvakh stepovoyi zony Ukrayiny [Epizootological monitoring of helminthic and protozoan diseases of poultry in industrial, farm and homestead farms of the steppe zone of Ukraine]. Bulletin of the Institute of Agriculture of the steppe zone of NAAS of Ukraine, 5, 157-161. (in Ukrainian)

Menon, D. G., Bennett, D. C., & Cheng, K. M. (2014). Understanding the Behavior of Domestic Emus: A Means to Improve Their Management and Welfare-Major Behaviors and Activity Time Budgets of Adult Emus. Journal of Animals, 2014, ID 938327. doi: 10.1155/2014/938327 Moreno, A. I., & Rendon, R. (2020). History and Current Situation of Commercial Ostrich Farming in Mexico. Journal of World s

Poultry Research, 9(4), 224-232. doi: 10.36380/jwpr.2019.28 Nemejc, K., & Lukesova, D. (2012). Parasite Fauna of Ostriches, Emus and Rheas. Agricultura Tropica et Subtropica, 45(1), 45-50.

doi: 10.2478/v10295-012-0007-6 Ola-Fadunsin, S. D., Uwabujo, P. I., Sanda, I. M., Ganiyu, I. A., Hussain, K., Rabiu, M., Elelu, N., & Alayande, M. O. (2019). Gastrointestinal helminths of intensively managed poultry in Kwara Central, Kwara State, Nigeria: Its diversity, prevalence, intensity, and risk factors. Veterinary World, 12(3), 389-396. doi: 10.14202/vetworld.2019.389-396 Paliy, A. P., Mashkey, A. M., Sumakova, N. V., & Paliy, A. P. (2018a). Distribution of poultry ectoparasites in industrial farms, farms,

and private plots with different rearing technologies. Biosystems Diversity, 26(2), 153-159. doi: 10.15421/011824 Paliy, A. P., Stegniy, B. T., Kuzminov, A. V., Buzun, A. I., Gerilovich, A. P., Bogach, M. V., & Stegniy, M. Y. (2020a). Effectiveness of aldehyde disinfectant "DZPT-2" against the African swine fever virus. Ukrainian Journal of Ecology, 10(3), 131 -138. doi : 10.15421 /2020_146

Paliy, A. P., Stegniy, B. T., Muzyka, D. V., Gerilovych, A. P., & Korneykov, O. M. (2016). The study of the properties of the novel

virucidal disinfectant. Agricultural Science and Practice, 3(3), 41 -47. doi: 10.15407/agrisp3.03.041 Paliy, A. P., Sumakova, N. V., Mashkey, A. M., Petrov, R. V., Paliy, A. P., & Ishchenko, K. V. (2018b). Contamination of animal-

keeping premises with eggs of parasitic worms. Biosystems Diversity, 26(4), 327-333. doi: 10.15421/011849 Paliy, A. P., Sumakova, N. V., Paliy, A .P., & Ishchenko, K. V. (2018c). Biological control of house fly. Ukrainian Journal of Ecology,

8(2), 230-234. doi: 10.15421 /2018_332 Paliy, A. P., Zavgorodniy, A. I., Stegniy, B. T., & Gerilovych, A. P. (2015). A study of the efficiency of modern domestic disinfectants

in the system of TB control activities. Agricultural Science and Practice, 2(2), 26-31. doi: 10.15407/agrisp2.02.026 Paliy, A. P., Zavgorodniy, A. I., Stegniy, B. T., & Palii, A. P. (2020b). Scientific and methodological grounds for controlling the

development and use of disinfectants. Monograph. Kharkiv: «Miskdruk», 318. ISBN: 978-617-619-237-4. (in Ukrainian) Paliy, A., Sumakova, N., Petrov, R., Shkromada, O., Ulko, L., & Palii, A. (2019). Contamination of urbanized territories with eggs of

helmiths of animals. Biosystems Diversity, 27(2), P. 118-124. doi: 10.15421 /011916 Papini, R., Girivetto, M., Marangi, M., Mancianti, F., & Giangaspero, A. (2012). Endoparasite Infections in Pet and Zoo Birds in

Italy. The Scientific World Journal, 2012, ID 253127. doi: 10.1100/2012/253127 Polishchuk, V. M., Tsekhmistrenko, S. I., Polishchuk, S. A., Ponomarenko, N. V., Rol, N. V., Cherniuk, S. V., Cherniavskyi, O. O., Kuzmenko, O. A., Prysiazhniuk, N. M., Karaulna, V. M., Lastovska, I. O., & Fedoruk, N. M. (2020). Age-related characteristics of lipid peroxidation and antioxidant defense system of ostriches (Struthio camelus domesticus). Ukrainian Journal of Ecology, 10(1), 168-174. doi: 10.15421/2020_29 Ponce Gordo, F., Herrera, S., Castro, A. T., Garcia Duran, B., & Martinez Diaz, R. A. (2002). Parasites from farmed ostriches (Struthio camelus) and rheas (Rhea americana) in Europe. Veterinary parasitology, 107(1 -2), 137-160. doi: 10.1016/s0304-4017(02)00104-8

Preston, S., Piedrafita, D., Sandeman, M., & Cotton, S. (2019). The current status of anthelmintic resistance in a temperate region of Australia; implications for small ruminant farm management. Veterinary parasitology, regional studies and reports, 17, 100313. doi: 10.1016/j.vprsr.2019.100313 Rafael, A. M. D., Beatriz, M. M., Luis, N. J., & Francisco, P. G. (2013). Gastrointestinal parasites in greater rheas (Rhea americana) and lesser rheas (Rhea pennata) from Argentina. Elsevier Science Bv, Veterinary Parasitology, 194(1), 5-2013, 75-78. doi: 10.1016/j.vetpar.2012.12.021

Ross, E. J., & Deeming, D. C. (1998). Feeding and vigilance behaviour of breeding ostriches (Struthio camelus) in a farming

environment in Britain. British poultry science, 39(2), 173-177. doi: 10.1080/00071669889088 Sotiraki, S. T., Georgiades, G., Antoniadou-Sotiriadou, K., & Himonas, C. A. (2001). Gastrointestinal parasites in ostriches (Struthio camelus). The Veterinary record, 148(3), 84-86. doi: 10.1136/vr.148.3.84

241

Endoparasic disease of ostriches

Springborn, M. R., Keller, R. P., Elwood, S., Romagosa, C. M., Zambrana-Torrelio, C., & Daszak, P. (2015). Integrating invasion and

disease in the risk assessment of live bird trade. Diversity and Distributions, 21(1), 101 -110. doi: 10.1111 /ddi.12281 Stegniy, B. T., Paliy, A. P., Pavlichenko, O. V., Muzyka, D. V., Tkachenko, S. V., & Usova, L. P. (2019). Virucidal properties of innovative disinfectant to Avian influenza virus and Newcastle disease virus. Journal for Veterinary Medicine, Biotechnology and Biosafety, 5 (3), 27-33. doi: 10.36016/JVMBBS-2019-5-3-6 Strashnyuk, D. V., & Kiritchenko, R. M. (2014). Osobennosti vyrashchivaniya Afrikans'kogo strausa (Struthio camelus) v usloviyakh Poles'ya ovenshchiny [Features growing African Ostrich (Struthio camelus) under Polissya Rivnenshchyna]. Scientific notes of Ternopil National Pedagogical University. Biology series, 4(61), 117-122. (in Ukrainian) Tomza-Marciniak, A., Pilarczyk, B., Tobianska, B., & Tarasewicz, N. (2014). Gastrointestinal parasites of free-range chickens.

Annals of parasitology, 60(4), 305-308. PMID: 25706430 Verwoerd, D. J. (2000). Ostrich diseases. Revue Scientifique et Technique (International Office of Epizootics), 19(2), 638-661. doi: 10.20506/rst.19.2.1235

Wang, J. X., Li, P., Zhang, X. T., & Ye, L. X. (2017). Developmental morphology study on the stomach of African ostrich chicks.

Poultry Science, 96(7), 2006-2012. doi: 10.3382/ps/pew504 Yuksek, N., Agaoglu, Z., Kaya, A., Aslan, L., Erdogan, H. M., & Akgul, Y. (2002). Stomach impaction in ostriches (Struthio camelus): blood chemistry, hematology, and treatment. Avian diseases, 46(3), 757-560. doi: 10.1637/0005-2086(2002)046[0757:SIIOSC]2.0.CO;2 Zavgorodniy, A. I., Stegniy, B. T., Paliy, A. P., Gorjeev, V. M., & Smirnov, A. M. (2013). Scientific and practical aspects of disinfection

in veterinary medicine. Kharkiv: FOP Brovin O.V., 222. ISBN 978-966-2445-59-6. (in Ukrainian) Zhang, R., Han, D., Ma, S., Luo, G., Ji, Q., Xue, S., Yang, M., & Li, J. (2017). Plantar pressure distribution of ostrich during locomotion on loose sand and solid ground. Peer J., 5, e3613. doi: 10.7717/peerj.3613

Citation:

Paliy, A.P., Sumakova, N.V., Petrov, R.V., Berezovskiy, A.V., Risovaniy, V.I., Zon, G.A., Ivanovskaya, L.B., Fotin, A.I., Dolbanosova, R.V., Livoshchenko, L.P., Livoshchenko, Ye.M., Palii, A.P. (2020). Endoparasic diseases of ostriches in eastern Ukraine. Ukrainian Journal of Ecology, 10(4), 235-241. I This work is licensed under a Creative Commons Attribution 4.0. License

i Надоели баннеры? Вы всегда можете отключить рекламу.