Научная статья на тему 'Comparative embryonic development of nematodes of the genus Тrichuris (Nematoda, Trichuridae) obtained from sheep (Ovis aries)'

Comparative embryonic development of nematodes of the genus Тrichuris (Nematoda, Trichuridae) obtained from sheep (Ovis aries) Текст научной статьи по специальности «Биологические науки»

CC BY
202
45
i Надоели баннеры? Вы всегда можете отключить рекламу.
Журнал
Biosystems Diversity
ESCI
Область наук
Ключевые слова
trichurosis / Trichuris оvis / Trichuris globulosa / nematode eggs / embryogenesis / in vitro / morphological changes / metric parameters

Аннотация научной статьи по биологическим наукам, автор научной работы — V. V. Melnychuk, А. V. Berezovsky

Biological specifics of Trichuris оvis Abildgaard, 1795 and T. globulosa Linstow, 1901 parasitizing domestic sheep were analyzed enhancing the species identification of these nematode species. The embryonic development of nematodes was timed, survival of embryonic stages was determined taking into account their morphological and metric specifics in laboratory culture. Trichuris eggs were isolated from gonads of adult female nematodes collected from caeca of dissected sheep. Then the eggs were cultured at optimal temperature to the formation of eggs with mobile larvae. Six morphologically distinct stages of embryogenesis were established in T. оvis and T. globulosa nematodes. The protoplast stage lasted from the 1st to the 12th day in T. оvis and to the 18th day in T. globulosa. Blastomeric formation occurred from the 3rd to the 18th day in T. оvis and from the 3rd to the 21st day in T. globulosa. Bean-shaped embryos formed from the 6th to the 21st day in T. оvis, and from the 9th to the 30th day in T. globulosa. Tadpole-like embryos developed from the 12th to the 24th day in T. оvis and from the 18th to the 33rd day in T. globulosa. Larvae formed in eggs of T. оvis from the 18th to the 27th day, and in eggs of T. globulosa from the 21st to the 36th day. Mobile larvae formed from the 21st to the 30th day in T. оvis, and from the 30th to the 39th day in T. globulosa. At 27 °С, mature eggs with mobile larvae developed in 30 days in T. оvis and in 39 in T. globulosa. The egg survival in laboratory culture was 84.3 ± 4.2 % and 76.3 ± 1.5%, respectively. Developmental changes of metric parameters in Trichuris nematode eggs (length and width of eggs, plug length, eggshell thickness) were species-specific.

i Надоели баннеры? Вы всегда можете отключить рекламу.

Похожие темы научных работ по биологическим наукам , автор научной работы — V. V. Melnychuk, А. V. Berezovsky

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

Текст научной работы на тему «Comparative embryonic development of nematodes of the genus Тrichuris (Nematoda, Trichuridae) obtained from sheep (Ovis aries)»

Biosystems

Diversitv

Biosystems

Diversity

ISSN 2519-8513 (Print) ISSN 2520-2529 (Online) Biosyst. Divers., 26(4), 257-262 doi: 10.15421/011839

Comparative embryonic development of nematodes of the genus Trichuris (Nematoda, Trichuridae) obtained from sheep (Ovis aries)

V. V. Melnychuk*, A V. Berezovsky**

*Lviv National University ofVeterinary Medicine and Biotechnologies named after S. Z. Gzhytskyj, Lviv, Ukraine **Sumy National Agrarian University, Sumy, Ukraine

Article info

Received 06.10.2018 Received in revised form

07.11.2018 Accepted 14.11.2018

Lviv National University of Veterinary Medicine and Biotechnologies named after S. Z. Gzhytskyj, Pekarska st., 50, Lviv, 79010, Ukraine. Tel.: +38-032-275-65-51. E-mail:

melnychuk86@ukr.net

Sumy National Agrarian University, Herasym Kondratiev st., 160, Sumy, 40000, Ukraine. Tel.: +38-054-262-78-16.

Introduction

Melnychuk, V. V., & Berezovsky, Á. V. (2018). Comparative embryonic development of nematodes of the genus Trichuris (Nematoda, Trichuridae) obtained from sheep (Ovis aries). Biosystems Diversity, 26(4), 257-262. doi:10.15421/011839

Biological specifics of Trichuris ovis Abildgaard, 1795 and T. globulosa Linstow, 1901 parasitizing domestic sheep were analyzed enhancing the species identification of these nematode species. The embryonic development of nematodes was timed, survival of embryonic stages was determined taking into account their morphological and metric specifics in laboratory culture. Trichuris eggs were isolated from gonads of adult female nematodes collected from caeca of dissected sheep. Then the eggs were cultured at optimal temperature to the formation of eggs with mobile larvae. Six morphologically distinct stages of embryogenesis were established in T. ovis and T. globulosa nematodes. The protoplast stage lasted from the 1st to the 12th day in T. ovis and to the 18th day in T. globulosa. Blastomeric formation occurred from the 3rd to the 18th day in T. ovis and from the 3rd to the 21st day in T. globulosa. Bean-shaped embryos formed from the 6th to the 21st day in T. ovis, and from the 9th to the 30th day in T. globulosa. Tadpole-like embryos developed from the 12th to the 24th day in T. ovis and from the 18th to the 33rd day in T. globulosa. Larvae formed in eggs of T. ovis from the 18th to the 27th day, and in eggs of T. globulosa from the 21st to the 36th day. Mobile larvae formed from the 21st to the 30th day in T. ovis, and from the 30th to the 39th day in T. globulosa. At 27 °Q mature eggs with mobile larvae developed in 30 days in T. ovis and in 39 in T. globulosa. The egg survival in laboratory culture was 84.3 ± 4.2 % and 76.3 ± 1.5%, respectively. Developmental changes of metric parameters in Trichuris nematode eggs (length and width of eggs, plug length, eggshell thickness) were species-specific.

Keywords: trichurosis, Trichuris ovis; Trichuris globulosa; nematode eggs; embryogenesis; in vitro; morphological changes; metric parameters

Nematodes of the genus Trichuris Schrank, 1788 are common parasitic pathogens of various wild and domestic animals. For example, they have been observed in the even-toed mammals (argali, roe deer, camels, bulls, boars, pigs), carnivores (foxes, dogs and wolves), and rodents (marmots, gerbils, mice and rats) (Fahmy, 1954; Salaba et al., 2003; Robles et al., 2006; Eichenberger et al., 2018). Trichuris pathogens infect humans too (Fincham & Markus, 2001; Kyung-Sun et al., 2009; Manz et al., 2017). There are more than 70 species in this genus, most of which are specific to certain host taxa. However, there are reports of possibility of infections in humans by non-specific nematode species (Dunn et al., 2002).

In domestic ruminants (cattle, sheep, goats), the most common species of this genus are T. skrjabini (Baskakov, 1924), T. ovis (Abildgaard, 1795) and T. globulosa (Linstow, 1901). For example, in Europe the Trichuris infection rates in sheep range from 41.8% to 100% (Salaba et al., 2013). In South-Western Turkey, T. skrjabini pathogens were found in 74% of examined sheep, T. ovis was recorded in 72% of studied animals (Umur & Yukari, 2005). In Nigeria, the most common Trichuris species in goats was T. ovis (72.5%), while T. globulosa was rarer (38.3%) (Nwosu et al., 1996). In certain regions of Sudan, T. globulosa was observed only in 0.1% and 0.6% of studied sheep and goats, respectively (Almalaik et al., 2008). The Trichuris species parasitizing in sheep in Ukraine are T. ovis (most common, abundance index 3.4 specimens), T. skrjabini (less common, abundance index 2.2 specimens), and T. globulosa (the rarest, abundance index 0.6 specimen) (Yevstafie-va et al., 2018). This dominance of certain nematode species over others, even in the same species, is usually linked to their adaptive capabilities

and tolerance of unfavourable environmental conditions. The parasitic habits which are known to be species-specific are seen in all its specimens and are secured in its phylogeny. Hence, adaptation is the main vital function, almost overdeveloped in parasites to preserve both individual and species survival. At the same time, the survival of a specimen depends, mostly, on feeding, while species survival is linked to its biological features (McSorley, 2003; Yazwinski & Tucker, 2006; Boyko et al., 2009, 2016; Blaxter & Koutsovoulos, 2015).

The development of Trichuris nematodes is direct, without an intermediate host. The main and deciding environmental factors in viability and durability of embryonic stages in these nematodes are the vegetation cover and also the temperature, the moisture of air and soil, landscape forms, rainfall, and other abiotic factors (Thapar & Singh, 1954; Mame-dova & Fataliev, 2009). Other researchers observe that the development of infectious eggs of Trichuris nematodes in the environment is principally influenced by temperature (Beer, 1788) or soil type (Brown, 1927).

It is known that the embryogenesis of Trichuris nematodes occurs in several stages. Some authors recognize the following stages of development of Trichuris eggs in the environment: nuclear fusion, first rest period, fission groove formation, second rest period, protoplasm clearing, larva formation, larva in one revolution, larva in two revolutions, formation of infectious larva (Fataliev, 2013). Other researchers note such embryonic periods in T. trichiura (Linnaeus, 1771): fertilized egg with two pronuclei, formation of 2 to 10 blastomeres, further cleavage, gastrulation, embryo with a closed blastopore, moving embryo, formed larva with a stylet (Malahov et al., 1984).

There are many studies of embryonic development of Trichuris nematodes which infect humans (Bundy & Cooper, 1989; Skriabyn et al., 1957). At the same time, certain aspects of embryonic development in

eggs of Trichuris nematodes of sheep are still insufficiently known. There are also rather counterintuitive data on the periods of egg development in nematodes of this genus (Skriabyn et al., 1957). Thus, the aim of the present work is to study the specifics of embryogenesis in nematodes of the species T. ovis and T. globulosa in vitro, taking into account the morphological and metric changes in the eggs.

Materials and methods

Nematodes were collected in during helminthological investigation of the large intestine of dead or slaughtered sheep (Skriabyn, 1928). The nematode species were identified using keys (Skriabyn et al., 1957; Iva-shkyn et al., 1989). To study the biological specifics of T. ovis and T. globulosa nematodes in laboratory culture, their eggs were collected from gonads of female nematodes. Each separate culture was placed in a Petri dish and cultured in a thermostat at 27 °C to the point of mobile larva formation. The cultures were examined every three days under a light microscope. The stage of development was identified by morphology of the embryo, also eggs that had stopped developing or were destroyed were counted. Each experiment was performed in triplicate.

Morphometric parameters of T. ovis and T. globulosa eggs (length and width of egg, length and width of egg plug, eggshell thickness) were studied in cultures, using the software Image J for Windows® (version 2.00) in interactive mode using 10x, 40x, 100x objective and 10x photo eyepiece. To calibrate the image analyzer, the ruled scale of the ocular micrometer was coincided with the scale of stage micrometer included in the MikroMed microscope kit. Microphotographs were taken using a digital camera of a MikroMed 5 Mpix (China) microscope.

Statistical processing of the experimental results was carried out using Statistica 10 (StatSoft Inc., 2011) software. Standard deviation (SD) and average values (x) were calculated. Significance of difference between average values in the studied egg cultures of Trichuris nematodes was established using one-way analysis of variance and F-test for 95% confidence level.

Results

It was established that embryogenesis of T. ovis and T. globulosa nematode parasites of sheep occurs in six stages in laboratory culture at 27 °C: protoplast, blastomeric formation, bean-like embryo, tadpole-like embryo, larva formation, and mobile larva formation. These stages are characterized by morphological changes in nematode eggs. At the protoplast stage, egg cytoplasm was filled with large granules which visually merged into one mass (Fig. 1a). Blastomeric formation was characterized by the cleavage and formation of two (Fig. 1b) and then three and more large cells, and the size of the blastomeres decreased in inverse proportion to their numbers (Fig. 1c). The bean-like embryo was morphologically distinct by the development of multicellular bean-shaped embryo in the egg (Fig. 1d). Later, the embryo changed into a shape resembling a tadpole, which was hence the tadpole-like embryo stage (Fig. 1e).The next stage was characterized by formation of motionless larva, with granular, slightly contoured body (Fig. 1f). The embryogenesis of the studied nematodes, regardless of the species, ended in mobile larva formation in the egg. The larva was twisted, completely filled the internal volume of the egg and actively moved under the influence of warmth, and also had a clear morphological structure (F ig. 1g).

Although the process of embryogenesis did not differ by morphologic changes in eggs of T. ovis and T. globulosa nematodes, their periods of development and survival were dissimilar. For example, eggs obtained from T. ovis female gonads in vitro at 27 °C developed mobile larvae in 30 days, and their survival was 84.3 ± 4.2% (Table 1).

All of the eggs (100.0%), obtained from female nematode gonads were protoplast. From the third to 12th day of culture, the eggs progressed to the second stage of development, formation and cleaving of blasto-meres. First, two blastomeres appeared (44.3 ± 3.1% at the third day), then three and more blastomeres (41.3 ± 1.2% at the sixth day, 41.7 ± 3.5% at the ninth day). From the sixth day, 8.0 ± 1.7% of all eggs were at the beanlike embryo stage. The maximum ratio of eggs on the third stage of development (54.7 ± 6.4 and 57.7 ± 8.1%) was recorded from the 12th to 15th

day of culture. At the 12th day of experiment, 5.3 ± 3.5% of T. ovis were observed to be developing from bean-like to tadpole-like stage.

g

Fig. 1. Embryonic stages of development in nematodes of the species T. ovis and T. globulosa parasitizing domestic sheep: a - protoplast, b - cleavage and formation of two blastomeres,

c - cleavage and formation of three and more blastomeres, d - formation of bean-like embryo, e - formation of tadpole-like embryo, f - larva formation, g - mobile larva formation

a

b

c

d

e

Maximum ratio of eggs at this stage was observed at the 21st day of culture (44.3 ± 4.0%). At the 18th day, 14.0 ± 4.4% of eggs contained formed, though motionless, larvae. The duration of that stage of development was until the 27th day of culture, with maximum ratio (50.3 ± 5.7%) on the 24th day of culture. Formation of mobile larvae started at the 21st day, when they comprised 10.3 ± 2.1% of all eggs. Subsequently, the ratio of eggs containing mobile larvae was 29.3 ± 2.5% at the 24th day, 81.3 ± 4.9% at the 27th day, and 84.3 ± 4.2% at the 30th day of experiment.

Also, 15.7 ± 4.2% of all eggs did not continue developing and died. In the study of the embryonic specifics of T. globulosa nematodes, their eggs were observed to mature to the mobile larvae stage more slowly compared to T. ovis nematodes. That development occurred in 39 days. At the same time, T. globulosa eggs were less viable: only 76.3 ± 1.5% developed into mature eggs, while 23.7 ± 1.5% of eggs did not develop and died (Table 2). The obtained cultures of T. globulosa eggs were all at the protoplast stage at the beginning of experiment. Further, the ratio of

protoplast egg decreased to 23.7 ± 1.5% at the 18th day. From the 3rd to 21st day of culture, blastomeric formation occurred in the eggs. Maximum ratio of eggs with two blastomeres was observed at the 3rd day (35.3 ± 2.1%), that of eggs with three and more blastomeres at the 6-9th days (39.7-41.3%). The bean-like stage of development was recorded at the 9th (23.0 ± 1.0%o of all eggs) to 30th day of culture. Their ratio increased to its maximum at 15th to 18th day (from 52.0 ± 3.0 to 54.0 ± 2.7%). From the 21st to 30th day of experiment, the numbers of eggs containing beanlike embryos gradually decreased with their development to the next stage, the tadpole-like embryo. That stage occurred from the 18th to 33rd days of culture. Maximum ratio of eggs with that embryonic stage was recorded at the 24th to 27th day of culture (39.7-42.3%). The larval formation was observed from the 21st day of experiment (11.3 ± 1.5%) to 43.7 ± 3.5% at the 30th day, the stage was observed till the 36th day. Mobile larva formation occurred in T. globulosa eggs from the 30th to 39th day of experiment, the ratio of the eggs with that stage increasing from 5.3 ± 2.1 to 76.3 ± 1.5%.

Table 1

Parameters of embryonic development of eggs obtained from Trichuris ovis gonads, in experimental culture (x ± SD, n = 100)

Stag e of development, %

culture protoplast 2 >3 - bean-like embryo tadpole-like embryo larva formation mobile larva formation arrested development

1 100.00 - - - - - - -

3 25.67 ± 2.08 44.33 ± 3.06 30.00 ± 1.73 - - - - -

6 19.67 ± 1.53 31.00 ± 2.00 41.33 ± 1.15 8.00 ± 1.73 - - - -

9 18.33 ± 0.58 6.67 ± 2.08 41.67 ± 3.51 33.33 ± 4.73 - - - -

12 15.67 ± 4.16 3.00 ± 1.00 21.33 ± 1.53 54.67 ± 6.35 5.33 ± 3.51 - - -

15 - 2.00 ± 1.00 12.00 ± 3.00 57.67 ± 8.14 12.67 ± 7.57 - - 15.67 ± 4.16

18 - - 3.67 ± 2.08 45.33 ± 5.13 21.33 ± 1.53 14.00 ± 4.36 - 15.67 ± 4.16

21 - - - 11.33 ± 2.52 44.33 ± 4.04 18.33 ± 2.08 10.33 ± 2.08 15.67 ± 4.16

24 - - - - 4.67 ± 2.52 50.33 ± 5.69 29.33 ± 2.52 15.67 ± 4.16

27 - - - - - 3.00 ± 1.73 81.33 ± 4.93 15.67 ± 4.16

30 - - - - - - 84.33 ± 4.16 15.67 ± 4.16

Table 2

Parameters of embryonic development of eggs obtained from Trichuris globulosa gonads, in experimental culture (x ± SD, n = 100)

Stage of development, %

i \ oi culture protoplast blastomere formation 2 >3 bean-like embryo tadpole-like embryo larva formation mobile larva formation arrested development

1 100.00 - - - - - - -

3 48.33 ± 2.08 35.33 ± 2.08 16.33 ± 2.08 - - - - -

6 33.00 ± 2.65 25.67 ± 2.08 41.33 ± 1.53 - - - - -

9 26.00 ± 1.73 11.33 ± 2.52 39.67 ± 1.53 23.00 ± 1.00 - - - -

12 23.67 ± 1.53 4.67 ± 1.53 35.67 ± 1.53 36.00 ± 2.65 - - - -

15 23.67 ± 1.53 2.33 ± 0.58 22.00 ± 1.73 52.00 ± 3.00 - - - -

18 23.67 ± 1.53 1.33 ± 0.58 11.00 ± 2.00 54.00 ± 2.65 10.00 ± 1.00 - - -

21 - - 2.00 ± 1.00 31.67 ± 1.53 31.33 ± 1.53 11.33 ± 1.53 - 23.67 ± 1.53

24 - - - 21.33 ± 1.53 39.67 ± 2.31 15.33 ± 0.58 - 23.67 ± 1.53

27 - - - 11.33 ± 1.15 42.33 ± 0.58 22.67 ± 2.08 - 23.67 ± 1.53

30 - - - 2.33 ± 1.53 25.00 ± 3.61 43.67 ± 3.51 5.33 ± 2.08 23.67 ± 1.53

33 - - - - 10.67 ± 1.53 37.67 ± 1.53 28.00 ± 2.00 23.67 ± 1.53

36 - - - - - 15.33 ± 4.51 61.00 ± 4.36 23.67 ± 1.53

39 - - - - - - 76.33 ± 1.53 23.67 ± 1.53

Morphometric study revealed that the sizes of T. ovis and T. Globulosa eggs changed during embryonic development, and that there were species-specific differences. The length and width of eggs obtained from T. ovis females at protoplast stage were 71.3 ± 1.7 and 32.7 ± 1.8 pm respectively, with egg plug length of 8.8 ± 1.1 pm and egg plug width of 10.7 ± 0.6 pm. Eggshell thickness of those eggs was 3.0 ± 0.2 pm, internal surface area was 1053 ± 82 pm2. Mature eggs containing mature larvae were statistically smaller (P < 0.05) by 3.4% (68.9 ± 1.3 pm) of egg length (Fig. 2a), 16.8% (2.5 ± 0.3 pm) of eggshell thickness (Fig. 2e) and 13.7% (7.6 ± 0.4 pm) length of egg plugs (Fig. 2c). Simultaneously, egg width increased to 35.1 ±1.2 pm (by 6.8%, P < 0.05) (Fig. 2b). There were no statistically significant differences in egg plug width (11.1 ± 0.6 pm) and internal surface area (1107 ± 31 pm2) during the studied embryogenesis (Fig. 2d,f).

In the study of metric parameters of eggs, it was established that their length and width at the protoplast stage were 70.8 ± 3.6 and 38.9 ± 1.6 pm respectively; length and width of egg plug were 3.3 ± 0.5 and 9.1 ± 0.4 pm, eggshell thickness was 4.1 ± 0.3 pm, internal surface area

was 1306 ± 51 pm . During embryogenesis, the eggs grew and developed: their length decreased by 4.9% (67.4 ± 3.7 pm, P < 0.05) (Fig. 3a), width decreased by 9.6% (3.7 ± 0.4 pm, P < 0.05) (Fig. 3e). Simultaneously, the egg width increased by 4.3% (38.9 ± 1.6 pm, P < 0.05) (Fig. 3b). During this time, egg plug length and width (3.1 ± 0.1 and 9.4 ± 0.4 pm) (Fig. 3c, d) and internal surface area (1338 ± 37 pm2) (Fig. 3f) were not statistically different. These changes point to the species-level biological specifics of T. ovis and T. globulosa, which also can influence their survival and abilities to adapt to inconstant environmental conditions.

Discussion

In the course of the present study, new data is collected on the embryogenesis of sheep nematode species T. ovis (Abildgaard, 1795) and T. globulosa (Linstow, 1901), on eggs obtained from nematode gonads. Knowledge of biological specifics, especially those of human parasites, factors into the regulation of their numbers, more so in the ecosystems experiencing anthropogenic pressure.

d

Fig. 2. Metric changes in Т. оvis eggs during embryogenesis: а - length, b - width, с - length of plug, d - width of plug, е - shell thickness (^m), f- internal surface area (^m2); А - protoplast, В - mobile larva formation; * - Р < 0.05 compared to egg parameters at protoplast stage; n = 10

Fig. 3. Metric changes in Т. globulosa eggs during embryogenesis: а - length, b - width, с - length of plug, d - width of plug, е - shell thickness (^m),f- internal surface area (^m2); А - protoplast, В - mobile larva formation; * - Р < 0.05 compared

to egg parameters at protoplast stage; n = 10

Also in several cases, such data is taken into account in species or genus identification (Liang et al., 2007; Wong & Candolin, 2015; Zvi-norova et al., 2016). According to scientific reports, trichurosis is very common in wild and domestic ruminants. The infection is recorded world-wide, with rates varying in different countries (Salaba et al., 2013; Yaro et al., 2015; Eichenberger et al., 2018). In our opinion, domination of one species over several other Trichuris species in a host population is to some degree dependent on the nematode specifics of embryogenesis which occurs outside the host. We observe that in vitro, at 27 °С the eggs of Т. avis develop faster (in 30 days) and are more viable (84.3 ± 4.2%) compared to the eggs of Т. globulosa (which develop to mobile larva stage in 39 days with 76.3 ± 1.5% survival). This may be the basis of domination of Т. avis over Т. globulosa in sheep in several regions of Ukraine (Yevstafieva et al., 2018).

Hence, we delineate the main morphological stages of development in eggs of Т. avis and Т. globulosa, which occur in the same way. The embryogenesis in the nematode species, studied at 27 °С, occurs in six stages: protoplast, blastomeric formation, bean-like embryo, tadpolelike embryo, larva formation, mobile larva formation. These stages of

development are quite morphologically distinct. Similar stages of development were found for T. suis (Schrank, 1788) nematodes obtained from pigs, and T. skrjabini (Baskakov 1924) roundworms, obtained from sheep (Yevstafieva et al., 2015, 2018). At the same time, quantitative indicators of changing embryonic stages in the development of Т. avis and Т. globulosa nematodes were different. For example, protoplast stage in T. avis occurs during the 1st to 12th days of culture, and from the 1st to 18th days of culture in T. globulosa. At the first day of culture, 100% of all eggs were at the protoplast stage. Blastomeric formation occurred from the 3rd to 18th days of culture in T. avis nematodes, and from the 3rd to 21st days of culture in T. globulosa, with maximum ratio of eggs with protoplasts, respectively, 41.7 ± 3.5% to 44.3 ± 3.1% and 35.3 ± 2.1% to 41.3 ± 1.5%. The bean-like embryo developed from the 6th to 21st days of culture in the eggs of T. avis, and from the 9th to 30th days of culture in the eggs of T. globulosa (the maximum ratios were respectively 57.7 ± 8.1% and 54.0 ± 2.7%). The tadpole-like embryo occurred in the eggs of T. avis from the 12th to 24th days of culture and in the eggs of T. globulosa from the 18th to 33rd days of culture. The maximum ratio of eggs with tadpole-like embryos were,

а

respectively, 44.3 ± 4.0% and 42.3 ± 0.6%. Larva formation occurred in the eggs of T. ovis from the 18th to 27th days of culture, and in the T. globulosa eggs from the 21st to 36th days of culture (maximum ratios were 50.3 ± 5.7 and 43.7 ± 3.5%, respectively). Mobile larva formation occurred in the eggs of T. ovis from the 21st to 30th day of culture, and in the eggs of T. globulosa from the 30th to 39th days of culture (maximum ratios were 84.3 ± 4.2 and 76.3 ± 1.5%). These data can be used in differential diagnostics of the studied Trichuris species. Most authors note that nematodes are identified by the morphology of adult specimens, especially the males (Bailey et al., 2009; Ghasemikhah et al., 2011). However, adult nematodes are not always available because they are obtained from dead hosts. In most cases, especially in diagnosing intestinal nematodes, coprologic samples are taken and only eggs are available. Some authors propose keys based on egg identification using various methods such as genetic analysis, electronic microscopy, dyeing and metric parameters (Palmer & McCombe, 1996; Sommer, 1996; Phosuk et al., 2018). Hence we propose new data on morphometric indicators of the eggs of T. ovis and T. globulosa and their changes in embryogenesis. We found that morphology of eggs obtained from gonads of the studied nematode species were not statistically different. The eggs were different by several metric parameters. For example, length and width of the eggs of T. ovis were 71.3 ± 1.7 and 32.7 ± 1.8 pm, and those of T. globulosa were 70.8 ± 3.6 and 38.9 ± 1.6 pm, and eggshell thickness was 3.03 ± 0.19 and 4.05 ± 0.25 pm respectively. Length and width of egg plug in T. ovis eggs were 8.8 ± 1.1 and 10.7 ± 0.6 pm, and those of T. globulosa were 3.3 ± 0.5 and 9.1 ± 0.4 pm, the internal surface areas were, respectively, 1053 ± 82 and 1306 ± 51 pm2. At the same time, embryogenesis in both species was characterized by species-specific changes of metric parameters. The mature eggs with mobile larva in T. ovis eggs were accompanied by decreasing egg length (by 3.4%, P < 0.05), eggshell thickness (by 16.8%, P < 0.05), egg plug length (by 13.7%, P < 0.05), and increasing egg width (by 4.3%, P < 0.05). The eggs of T. globulosa grew and developed with decreasing length (by 4.9%, P < 0.05), eggshell thickness (by 9.6%, P < 0.05), and increasing egg width (by 4.3%, P < 0.05). Our data increase the knowledge of biological features of T. ovis and T. globulosa nematodes.

Conclusion

The study showed that it is possible to use embryonic specifics (morphometric changes of eggs, periods of development, survival ratio) of nematodes of domestic sheep ( Ovis aries) of the genus Trichuris Roederer, 1761 in species identification. Six stages of embryonic development are recognized in Trichuris eggs: protoplast, blastomeric formation, bean-like embryo, tadpole-like embryo, larva formation and mobile larva formation. The stages are similar in T. ovis (Abildgaard, 1795) and T. globulosa (Linstow, 1901) nematodes. The differentiating species characters of T. ovis and T. globulosa are times of development and quantitative parameters of each embryonic stage. At 27 °C in vitro, maximum numbers of mature T. ovis eggs occur at the 30th day of culture with 84.3% survival. The embryonic development of T. globulosa in culture is longer, it takes place in 39 days, with lower survival of 76.3%. Metric changes of the eggs of T. ovis and T. globulosa during embryogenesis occur dissimilarly, pointing to their species differences. Formation of the mature eggs with mobile larva in T. ovis is accompanied by increasing egg width and decreasing eggshell thickness, egg length and egg plug length. In T. globulosa, the morphometric characters of eggs during embryonic development are characterized by decreasing length and eggshell thickness, with increasing egg width. These data have an application value in identifying the studied Trichuris species by collected eggs.

References

Almalaik, A. H. A., Bashar, A. E. & Abakar, A. D. (2008). Prevalence and dynamics of some gastrointestinal parasites of sheep and goats in Tulus Area based on post-mortem examination. Asian Journal of Animal and Veterinary Advances, 3, 390-399. Bailey, J. N., Kahn, L. P., & Walkden-Brown, S. W. (2009). The relative contributions of T. colubriformis, T. vitrinus, T. axei and T. rugatus to sheep infected

wilh Trichostrongylus spp. on 1he northern tablelands of New South Wales. Veterinary Parasitology, 165(1-2), 88-95.

Beer, R. J. (1788). Sludies on 1he biology of 1he life-cycle of Trichuris suis Schrank, 1788. Parasitology, 67(3), 253-262.

Blaxter, M., & Koutsovoulos, G. (2015). The evolution of parasitism in Nematoda. Parasitology, 142(l), 26-39.

Boyko, A., Brygadyrenko, V., Shendryk, L., & Loza, I. (2009). Estimation of the role of antopo-zoonosis invasion agente in the counteraction to bioterrorism. Counteraction to Chemical and Biological Terrorism in East European Countries. NATO Science for Peace and Security Series A: Chemistry and Biology. Springer Nature, 309-315.

Boyko, O. O., Zazharska, N. M., & Brygadyrenko, V. V. (2016). The influence of the extent of infestation by helminths upon changes in body weight of sheep in Ukraine. Visnyk of Dnipropetrovsk University. Biology, Ecology, 24(1), 3-7.

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

Brown, H. W. (1927). Studies on the eate of development and viability of the eggs of Ascaris lumbricoides and Trichuris trichiura under field conditions. Journal of Parasitology, 14(1), 1-15.

Bundy, D. A., & Cooper, E. S. (1989). Trichuris and trichuriasis in humans. Advances in Parasitology, 28, 107-173.

Dunn, J. J., Columbus, S. T., Aldeen, W. E., Davis, M., & Carroll, K. C. (2002). Trichuris vulpis recovered from a patient with chronic diarrhea and five dogs. Journal of Clinical Microbiology, 40(7), 2703-2704.

Eichenberger, R. M., Talukder, M. H., Field, M. A., Wangchuk, P., Giacomin, P., Loukas, A., & Sotillo, J. (2018). Characterization of Trichuris muris secreted proteins and extracellular vesicles provides new insights into host-parasite communication. Journal of Extracellular Vesicles, 7(1), 1428004.

Fahmy, M. A. M. (1954). An investigation on the life cycle of Trichuris muris. Parasitology, 44(1-2), 50-57.

Fataliev, G. G. (2013). Influence of abiotic factors on the embryonal development of Trichocephalus myocastoris (Nematoda, Trichocephalidae). Zoological Journal, 92(12). 1475-1477.

Fincham, J. E., & Markus, M. B. (2001). Human immune response to Trichuris trichiura. Trends in Parasitology, 17(3), 121.

Ghasemikhah, R., Mirhendi, H., Kia, E., Mowlavi, G., Sarmadian, H., Meshgi, B., Golestan, B., & Mobedi, I (2011). Morphological and morphometrical description of Trichostrongylus species isolated from domestic ruminants in Khuzestan province, Southwest Iran. Iranian Journal of Parasitology, 6(3), 82-88.

Ivashkin, V. M., Oripov, A. O., & Sonin, M. D. (1998). Opredelitel' gel'mintov melkogo rogatogo skota [Key to the helminths of small ruminants]. Russian Academy of Sciences, Moscow (in Russian).

Liang, S., Seto, E. Y., Remais, J. V., Zhong, B., Yang, C., Hubbard, A, Davis, G. M., Gu, X., Qiu, D., & Spear, R. C. (2007). Environmental effects on parasitic disease transmission exemplified by schistosomiasis in Western China. Proceedings of the National Academy of Sciences, 104(17), 7110-7115.

Malakhov, V. V., Romashov, B. Y., & Spiridonov, S. E. (1984). Embrional'noe razvitie Trichocephalus trichiurus i Eucoleus oesophagicola (Nematoda, Trichocephalidae) [Embryonic development of Trichocephalus trichiura and Eucoleus oesophagicola (Nematoda, Trichocephalidae)]. Journal of Parasitology, 18(4), 286-290 (in Russian).

Mamedova, M. M., & Fataliev, G. H. (2009). The development of the Trichocepha-lus ovis eggs in different sort of land. Journal of Veterinary Medicine, 4, 28-32.

Manz, K. M., Clowes, P., Kroidl, I., Kowuor, D. O., Geldmacher, C., Ntinginya, N. E., Maboko, L., Hoelscher, M., & Saathoff, E. (2017). Trichuris trichiura infection and its relation to environmental factors in Mbeya Region, Tanzania: A cross-sectional, population-based study. PLoS One, 12(4), e0175137.

McSorley, R. (2003). Adaptations of Nematides to environmental extremes. Florida Entomologist, 86(2), 138-142.

Nwosu, C. O., Ogunrinade, A. F., & Fagbemi, B. O. (1996). Prevalence and seasonal changes in the gastro-intestinal helminths of Nigerian goats. Journal of Helminthology, 70(4), 329-333.

Ok, K. S., Kim, Y. S., Song, J. H., Lee, J. H., Ryu, S. H., Lee, J. H., Moon, J. S., Whang, D. H., & Lee, H. K. (2009). Trichuris trichiura infection diagnosed by colonoscopy: Case reports and review of Korean literature. Journal of Parasitology, 47(3), 275-280.

Palmer, D. G., & McCombe, I. L. (1996). Lectin staining of trichostrongylid nematode eggs of sheep: Rapid identification of Haemonchus contortus eggs with peanut agglutinin. International Journal for Parasitology, 26(4), 447-450.

Phosuk, I., Sanpool, O., Thanchomnang, T., Sadaow, L., Rodpai, R., Anamnart, W., Janwan, P., Wijit, A, Laymanivong, S., Pa Aung, W. P., Intapan, P. M., & Maleewong, W. (2018). Molecular identification of Trichuris suis and Trichuris trichiura eggs in human populations from Thailand, Lao PDR, and Myanmar. The American Journal of Tropical Medicine and Hygiene, 98(1), 39-44.

Robles Mdel, R., Navone, G. T., & Notarnicola, J. (2006). A new species of Trichuris (Nematoda: Trichuridae) from Phyllotini rodents in Argentina. Journal of Parasitology, 92(1), 100-104.

Salaba, O., Rylkova, K., Vadlejch, J., Petrtyl, M., Schankova, S., Brozova, A., Jankovska, I., Jebavy, L., & Langrova, I. (2013). The first determination of

Trichuris sp. from roe deer by amplification and sequenation of the ITS1-5.8S-ITS2 segment of ribosomal DNA. Parasitology Research, 112(3), 955-960.

Skrjabin, K. I. (1928). Metod polnyh gel'mintologicheskih vskrytij pozvonochnyh, vkljuchaja cheloveka [The method of complete helminthological autopsy of vertebrates, including humans]. Moscow State University, Moscow (in Russian).

Skrjabin, K. I., Shikhobalova, N. P., & Orlov, I. V. (1957). Osnovy nematodolo-gii. Trihocefalidy i kapilljariidy zhivotnyh i cheloveka i vyzyvaemye imi zabolevanija [Trichocephalids and capillariids of animals and man and the diseases caused by them. The essentials of nematodology]. Russian Academy of Sciences, Moscow (in Russian).

Sommer, C. (1996). Digital image analysis and identification of eggs from bovine parasitic nematodes. Journal of Helminthology, 70(2), 143-151.

Thapar, G. S., & Singh, K. S. (1954). Studies on the life-history of Trichuris ovis (Abildgaard, 1795) (fam. Trichuridae: Nematoda). Proceedings of the Indian Academy of Sciences, 40(3), 69-88.

Umur, §., & Yukari, B. A. (2005). An Abattoir Survey of gastro-intestinal nematodes in sheep in the Burdur Region, Turkey. Turkish Journal of Veterinary and Animal Sciences, 29(5), 1195-1201.

Wong, B. B. M., & Candolin, U. (2015). Behavioral responses to changing environments. Behavioral Ecology, 26(3), 665-673.

Yaro, M. B., Naphtali, R S., & Tumba, D. P. (2015). A faecal survey of gastro-intestinal parasites in sheep and goats in Madagali Local Government Area, Adamawa State, Nigeria. Journal of Agriculture and Veterinary Science, 8(6), 22-25.

Yazwinski, T. A., & Tucker, C. A. (2006). A sampling of factors relative to 1he epidemiology of gastrointestinal nematode parasites of cattle in the United States. Veterinary Clinics of North America: Food Animal Practice, 22(3), 501-527.

Yevstafieva, V. A., Yuskiv, I. D., Melnychuk, V. V., Yasnolob, I. O., Kovalenko, V. A., & Horb, K. O. (2018). Nematodes of the genus Trichuris (Nematoda, Trichuridae) parasitizing sheep in central and south-eastern regions of Ukraine. Vestnik Zoologii, 52(3), 553-556.

Yevstafieva, V. A, Melnichuk, V. V., Sharavara, T. A., Sirenko, E. V., Makarevich, N. A., Kutsenko, Y. P., & Khlevnaya, G. S. (2018). Osobennosti embrional'-nogo razvitija jaic nematod Trichuris skrjabini (Baskakov 1924), parazitiru-jushhih u ovec [Specific features of embryonic development of Trichuris skrjabini (Baskakov, 1924) nematode eggs parasitizing in sheep]. An Agrarian Science of Euro-North-East, 62(1), 65-69 (in Russian).

Yevstafieva, V. А., Yuskiv, I. D., & Melnychuk, V. V. (2015). An investigation of embryo and eggshell development in Trichuris suis (Nematoda, Trichuridae) under laboratory conditions. Vestnik Zoologii, 50(2), 173-178.

Zvinorova, P. I., Halimani, T. E., Muchadeyi, F. C., Matika, O., Riggio, V. & Dzamaa, K. (2016). Prevalence and risk factors of gastrointestinal parasitic infections in goats in low-input low-output farming systems in Zimbabwe. Small Ruminant Research, 143, 75-83.

i Надоели баннеры? Вы всегда можете отключить рекламу.