Speed of Hatching and the Resistance of Chickens to Ascaridia Galli

Speed of Hatching and the Resistance of Chickens to Ascaridia Galli

Speed of Hatching and the Resistance of Chickens to Ascaridia Galli BERNARD B. R I E D E L Disease Research, Poultry Department, University of Georgia...

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Speed of Hatching and the Resistance of Chickens to Ascaridia Galli BERNARD B. R I E D E L Disease Research, Poultry Department, University of Georgia, Athens, Georgia (Received for publication March 17, 1950)

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VIDENCE has been presented which indicated that the resistance of chickens to infection by the large roundworm may be affected by several factors. Among these factors are genetic constitution (Ackert and Wilmoth, 1934; and Ackert et al., 1935a) and diet (Ackert and Beach, 1933; Ackert et al.-, 1927; Ackert and Spindler, 1929; and Riedel and Ackert, 1950a). Age as a factor of resistance was reported by Herrick (1926); Ackert et al. (1935b); and Riedel and Ackert (1950b). Histological studies made by Ackert and Edgar (1938) disclosed a progressive increase of goblet cells in the chicken duodenum. This increase of the number of goblet cells correlated with the increase of age resistance established formerly by Herrick (1926). The mucus secreted by the goblet cells was tested (Ackert, Todd and Tanner, 1938; and Frick and Ackert, 1948) and the results showed that the growth of young Ascaridia was retarded when placed in nutrient media containing autoclaved mucin from older chickens. Hydrogen-ion concentration as a factor in age resistance to the fowl ascarid was studied by Riedel and Ackert (1947). The fact that the worm habitat in chickens 17 to 35 weeks of age had about the same hydrogen-ion concentration as did that of young birds one to 8 weeks of age eliminated hydrogen-ion concentration as a factor of age resistance. Recently, Henderson and Champion

(1948) found that within breeds there was a tendency for chicks which hatched earliest to be the largest at the end of an 8-week period. As a result of their observations an investigation was undertaken to note if speed of hatching may influence the resistance of the chick toward infection by Ascaridia galli. METHODS

The chicks used in this investigation were selected from several hatchings of Rhode Island Reds after separating each hatch into an early, intermediary, and late period. To make certain that the speed of hatching between the early and late chicks varied considerably, the intermedial period, from which no chickens were taken, was always of 10 or more hours duration. The chickens in each experiment were banded and weighed within one week after hatching. The chicks were individually infected with 300 embryonated Ascaridia galli ova and autopsied 21 days later. The nematodes harbored in the intestinal lumen of each chick were collected and counted and the numbers of worms harbored by each bird were used as the criterion in determining the correlation between the degree of resistance to infection by Ascaridia galli and speed of hatching. RESULTS AND DISCUSSION

The data in Tables 1 and 2 show the effect of speed of hatching upon the weight 703

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BERNARD B. RIEDEL TABLE 1.—The effect of early and late hatching upon the weight records and the numbers of "Ascardia galli" harbored in younger chickens Number of birds harboring worms

Av. weight (gms.)

G

™P**

1 2

SSr

At start

At finish

Total worm number

Av. worm number harbored

30 31

60

52

Experiment 1 238 247

16 14

460 360

15.3 11.9

26 20

64 69

Experiment Z 20 240 19 253

826 856

31.8 42.8

29 24

58 60

Experiment 3 247 25 21 259

728 555

25.1 23.1

23 23

65 68

Experiment 4 244 21 260 20

644 578

28.0 25.1

22 23

69 71

Experiment 5 251 21 262 12

129 29

5.9 1.3

25 24

62 65

Experiment 6 17 239 15 253

58 96

2.3 4.0

2,845 2,474

18.4 17.1

Totals 1 2 ;

155 145

63 66

245 257

120 101

Group 1 hatched late, Group 2 hatched early.

records and the average numbers of Ascaridia galli harbored by growing chickens. In the first part of this investigation in which the chicks were infected at less than 10 days of age and autopsied 21 days later (Table 1), a consistent correlation existed between the speed of hatching and the average weight records. The chickens which hatched the earliest (Group 2) had a total, average weight of 12 grams higher than that of the chicks which hatched late (Group 1). With respect to Ascaridia the results were inconsistent. In two of the six experiments the group 2 chickens harbored more worms than the group 1 chickens. When the average, total number of worms from groups 1 and 2 were compared, the

first group was noted to harbor an average of 1.3 worms more. This small difference indicated a lack of correlation between the speed of hatching and the degree of resistance. The data in Table 2 were taken from chickens infected with Ascaridia during the sixth week of age and autopsied 21 days later. In five of the six experiments the average weight records were higher among the chickens which hatched the earliest. The group 2 chickens had a total, average weight 16 grams higher than those in group 1. Pertaining to the average worm numbers harbored by the chickens in each experiment (Table 2), the group 2 chickens harbored consistently fewer ascarids than did the group 1 birds. These small

SPEED OF HATCHING AND RESISTANCE OF CHICKS TO ASCARIDIA

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TABLE 2.—The effect of early and late hatching upon the weight records and the numbers of "Ascardia galli" harbored in older chickens Av. weight (gms.) Group*

1 2

Chick number

At start

Number of chickens harboring worms

At finish

Total worm number harbored

Av. worm number harbored

24 24

68 73

Experiment 1 885 997

32 24

1.3 1.0

25 22

71 74

Experiment 2 1,026 1,016

40 22

1.6 1.0

21 21

64 66

1,015 1,069

12 12

84 44

4.0 2.1

23 21

65 67

Experiment 4 1,001 1,049

16 11

62 34

2.7 1.6

20 20

68 71

Experiment 5 1,019 1,032

14 10

50 44

2.5 2.2

21 23

69 72

Experiment 6 1,008 998

11 9

66 54

3.1 2.3

69 51

334 222

2.5 1.7

Totals 1 2

134 131

68 71

1,008 1,026

Group 1 hatched late, Group 2 hatched early.

differences were not significant, and failed to show any correlation between speed of hatching and susceptibility to ascariasis in older chickens. The chickens in experiments 5 and 6 in Table 1 harbored fewer worms than the chickens in the remaining experiments. This may be explained on the basis that the infective ova used in the last two experiments were from cultures with a lower viability. From experience it has been observed that in every flock of chickens experimentally infected with infective ascarid ova, there are always some which are naturally immune and regardless of the age of the host when infected or the size of the infective dose, do not become infected. From the results of this investi-

gation it is apparent that the natural immunity was the greatest among the chicks which hatched the earliest, because fewer of these chicks harbored worms. SUMMARY

An experiment was performed to learn if speed of hatching affected the resistance of chickens toward infection by Ascaridia galli. The results indicated that the chickens which hatched the earliest grew more rapidly than those which hatched late. The speed of hatching did not correlate with the numbers of worms harbored. The natural immunity among the early hatched chicks was higher than it was among those hatching late, because fewer birds in the former category harbored worms.

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NEWS AND NOTES REFERENCES

Ackert, J. E., and T. D. Beach, 1933. Resistance of chickens to the nematode, Ascaridia lineata, affected by dietary supplements. Tr. Am. Micr. Soc. 52: 51-58. ——— and S. A. Edgar, 1938. Goblet cells and age resistance to parasitism. J. Parasitol. (Supp.) 24: 13-14. , L. L. Eisenbrandt, J. H. Wilmoth, B. Glading and I. Pratt, 1935a. Comparative resistance of five breeds of chickens to the nematode Ascaridia lineata (Schneider). J. Agric. Res. 607-624. —, W. L. Fisher and N. B. Zimmerman, 1927. Resistance to parasitism affected by the fatsoluble vitamin A. J. Parasitol. 13: 219-220. , D. A. Porter and T. D. Beach, 1935b. Age resistance of chickens to the nematode Ascaridia lineata (Schneider). J. Parasitol. 21:205-213. , and L. A. Spindler, 1929. Vitamin D and resistance of chickens to parasitism. Am. J. Hyg. 9: 292-307. , A. C. Todd and W. A. Tanner, 1938. Growing larvae Ascaridia lineata (nematode) in vitro. Tr. Am. Micr. Soc. 57: 292-296.

and J. H. Wilmoth, 1934. Resistant and susceptible strains of White Minorca chickens to the nematode Ascaridia lineata (Schneider). J. Parasitol. 20: 323-324. Frick, L. P. and J. E. Ackert, 1948. Further studies on duodenal mucus as a factor in age resistance of chickens to parasitism. J. Parasitol. 34: 192206. Henderson, E. W. and L. R. Champion, 1948. Correlation between speed of hatching and growth rate of chickens. Poultry Sci. 27: 667. Herrick, C. A., 1926. Studies on the resistance of chickens to the nematode, Ascaridia perpicillum. Am. J. Hyg 6: 153-172. Riedel, B. B. and J. E. Ackert, 1947. Further studies on hydrogen-ion concentration as a factor in age resistance to the fowl ascarid. J. Parasitol. (Suppl.) 33: 19-20. and , 1950a. The resistance of chickens to ascarids as affected by protein supplements of soybean oil meal and skim milk. Poultry Sci. 29:437-443. —•—— and , 1950b. Quantity and source of proteins as factors in resistance of chickens to ascarids. J. Parasitol. In press.

News and Notes {Continued from page 684)

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