IN VITRO DEVELOPMENT OF Ascaridia galli EGGS INTO INFECTIVE EGGS AND LARVAE OF STADIUM 2 (L2)

The study aimed at finding out the development of Ascaridia galli (A. gall) eggs that were given aerator treatment and those without aerator treatment into infective eggs and L2 through in vitro culture. Each treatments has 108,000 eggs assigned to 8 groups of 1,000; 2,000; 3,000; 4,000; 5,000; 6,00...

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Main Authors: Wida Wahidah Mubarokah, Kurniasih Kurniasih, Wisnu Nurcahyo, Joko Prastowo
Format: Article
Language:English
Published: Universitas Syiah Kuala 2019-06-01
Series:Jurnal Kedokteran Hewan
Subjects:
Online Access:https://jurnal.usk.ac.id/JKH/article/view/12978
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author Wida Wahidah Mubarokah
Kurniasih Kurniasih
Wisnu Nurcahyo
Joko Prastowo
author_facet Wida Wahidah Mubarokah
Kurniasih Kurniasih
Wisnu Nurcahyo
Joko Prastowo
author_sort Wida Wahidah Mubarokah
collection DOAJ
description The study aimed at finding out the development of Ascaridia galli (A. gall) eggs that were given aerator treatment and those without aerator treatment into infective eggs and L2 through in vitro culture. Each treatments has 108,000 eggs assigned to 8 groups of 1,000; 2,000; 3,000; 4,000; 5,000; 6,000; 7,000; and 8,000 eggs, respectively with 3 repetitions. Female A. galli were collected from the small intestinal lumen of naturally infected domestic chickens. The eggs collected from the uterus of adult female A. galli were incubated in sterile aquadest at ambient temperature for 45 days (without aerator) and 25 days (with aerator) to obtain the infective eggs and the L2. The number of the infective eggs and hatched L2 were counted under stereo microscope. Data were analysed descriptively. There were 97.740 eggs (90.5%) in the groups without aerator developed into infective eggs and 77,040 eggs (71.3%) developed into the L2. Meanwhile, there were 101,847 eggs (94.3%) in the groups with the aerator developed into the infective eggs and88.722 eggs (82.15%) hatched L2. It is concluded that the eggs collected from worms uterus had high viability and the aerator application shortened the developing period of the A. galli worms.
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spelling doaj.art-8b7d8a8ba68540189b7ef1726dd8ae052024-04-28T08:37:47ZengUniversitas Syiah KualaJurnal Kedokteran Hewan1978-225X2502-56002019-06-0113110.21157/j.ked.hewan.v13i1.129789938IN VITRO DEVELOPMENT OF Ascaridia galli EGGS INTO INFECTIVE EGGS AND LARVAE OF STADIUM 2 (L2)Wida Wahidah Mubarokah0Kurniasih Kurniasih1Wisnu Nurcahyo2Joko Prastowo3Doctoral Program Parasitology Department, Faculty of Veterinary Medicine, Universitas Gadjah Mada, Yogyakarta Department of Animal Health, Polytechnique of Agricultural Development Yogyakarta MagelangDepartment of Pathology, Faculty of Veterinary Medicine, Universitas Gadjah Mada, YogyakartaDepartment of Parasitology, Faculty of Veterinary Medicine, Universitas Gadjah Mada, YogyakartaDepartment of Parasitology, Faculty of Veterinary Medicine, Universitas Gadjah Mada, YogyakartaThe study aimed at finding out the development of Ascaridia galli (A. gall) eggs that were given aerator treatment and those without aerator treatment into infective eggs and L2 through in vitro culture. Each treatments has 108,000 eggs assigned to 8 groups of 1,000; 2,000; 3,000; 4,000; 5,000; 6,000; 7,000; and 8,000 eggs, respectively with 3 repetitions. Female A. galli were collected from the small intestinal lumen of naturally infected domestic chickens. The eggs collected from the uterus of adult female A. galli were incubated in sterile aquadest at ambient temperature for 45 days (without aerator) and 25 days (with aerator) to obtain the infective eggs and the L2. The number of the infective eggs and hatched L2 were counted under stereo microscope. Data were analysed descriptively. There were 97.740 eggs (90.5%) in the groups without aerator developed into infective eggs and 77,040 eggs (71.3%) developed into the L2. Meanwhile, there were 101,847 eggs (94.3%) in the groups with the aerator developed into the infective eggs and88.722 eggs (82.15%) hatched L2. It is concluded that the eggs collected from worms uterus had high viability and the aerator application shortened the developing period of the A. galli worms.https://jurnal.usk.ac.id/JKH/article/view/12978ascaridia galliinfective eggsin vitrolarvae of stadium 2
spellingShingle Wida Wahidah Mubarokah
Kurniasih Kurniasih
Wisnu Nurcahyo
Joko Prastowo
IN VITRO DEVELOPMENT OF Ascaridia galli EGGS INTO INFECTIVE EGGS AND LARVAE OF STADIUM 2 (L2)
Jurnal Kedokteran Hewan
ascaridia galli
infective eggs
in vitro
larvae of stadium 2
title IN VITRO DEVELOPMENT OF Ascaridia galli EGGS INTO INFECTIVE EGGS AND LARVAE OF STADIUM 2 (L2)
title_full IN VITRO DEVELOPMENT OF Ascaridia galli EGGS INTO INFECTIVE EGGS AND LARVAE OF STADIUM 2 (L2)
title_fullStr IN VITRO DEVELOPMENT OF Ascaridia galli EGGS INTO INFECTIVE EGGS AND LARVAE OF STADIUM 2 (L2)
title_full_unstemmed IN VITRO DEVELOPMENT OF Ascaridia galli EGGS INTO INFECTIVE EGGS AND LARVAE OF STADIUM 2 (L2)
title_short IN VITRO DEVELOPMENT OF Ascaridia galli EGGS INTO INFECTIVE EGGS AND LARVAE OF STADIUM 2 (L2)
title_sort in vitro development of ascaridia galli eggs into infective eggs and larvae of stadium 2 l2
topic ascaridia galli
infective eggs
in vitro
larvae of stadium 2
url https://jurnal.usk.ac.id/JKH/article/view/12978
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