INCIDENCE OF INTERNAL PARASITES OF DESERT GOATS IN NEW VALLEY, EGYPT

Document Type : Research article

Author

Animal Healthy Research Institute, New-Valley Laboratory

Abstract

 
The study was carried out on 515 goats from different localities in NewValley governorate with different ages and sexes during the period from May 2007 to May 2008. The study aimed to monitor parasitic infection among these goats qualitatively and quantitively. The results proved that 455 goats infected with different gastrointestinal parasites (88.34%) where Eimeria spp. was representing  an incidence of 78.02% while the total infection rate of different helminthes was 55.16% (40.55% in kids and 64.72 % in Adult). The infection rates were 35, 16% for Nematodes, 3.95% for Cestods, 16.03% for Trematods. The study declared that parasitic infection represents a major health impact on goats at New Valley with special reference to Eimeria spp. and Hemonchus contortus in both young and adults. The influence of seasonal variation proved higher coccidial infection at winter (86.7%), however higher intestinal helminths infection were found at spring and summer. It could be concluded that periodical parasitic examination of goats in NewValley should be attempted to recognize and manage parasitic infection.
 

Keywords


Animal Healthy Research Institute,

New-Valley Laboratory

 

Incidence of internal parasites of desert goats in New Valley, Egypt

(With 5 Tables and 4 Figures)

 

By

F.A. Osman

(Received at 18/11/2008)

 

معدل انتشار الطفيليات الداخلية فى الماعز الصحراوية

فى الوادى الجديد - مصر

 

فتحى احمد عثمان

 

استهدفت الدراسة حساب معدل انتشار الإصابة بالطفيليات الداخلية للماعز في الوادي الجديد وعلاقتها ببعض العوامل البيئية والبيولوجية المحيطة، حيث تم إجراء الفحص الطفيلي لعدد 515 حيوان من أعمار مختلفة وکلا الجنسين من أماکن مختلفة في الوادي الجديد (300 من الخارجة, 215 من الداخلة) خلال الفترة من مايو 2007 الى مايو 2008 وذلک بإجراء الفحص الکمي والکيفي للإصابة الطفيلية حيث شملت الدراسة عد البيض کدليل على معدل انتشار الإصابة. أوضحت النتائج أن 455 من الماعز کانت موجبة للاصابة الطفيلية (88.34%)، منهم 78.02% للکوکسيديا، 55.16 % لباقي الديدان المعوية (40.55 % في الصغار و 64.72 % للکبار) کما أشارت الدراسة ان نسبة الاصابة بالديدان الاسطوانية 35.16 % والديدان الشريطية 3.95 % والديدان المفلطحة 16.03. وبدراسة تأثير التغيرات الموسمية على نسبة الإصابة بالطفيليات المختلفة فقد سجل الشتاء اعلي نسبة اصابة بالکوکسيديا (86.7%) بينما سجل فصلى الربيع والصيف اعلى نسبة إصابة بالديدان المعوية. أوضحت الدراسة أيضا أن ديدان الهيمونکس قد سجلت 3.33% فى الماعز أقل من سنة, 14.54% في الماعز البالغة. مما سبق يتضح أهمية فحص الماعز للوقوف على نوعية ومدي إصابتها بالطفيليات بأنواعها والتي تسبب خسارة اقتصادية کبيرة ومن ثم يمکن وضع برامج للمکافحة وتقليل العدوى بعمل فحص دوري للماعز وتجريعها بصفة دورية بمضادات الديدان.

 

SUMMARY

 

The study was carried out on 515 goats from different localities in NewValley governorate with different ages and sexes during the period from May 2007 to May 2008. The study aimed to monitor parasitic infection among these goats qualitatively and quantitively. The results proved that 455 goats infected with different gastrointestinal parasites (88.34%) where Eimeria spp. was representing  an incidence of 78.02% while the total infection rate of different helminthes was 55.16% (40.55% in kids and 64.72 % in Adult). The infection rates were 35, 16% for Nematodes, 3.95% for Cestods, 16.03% for Trematods. The study declared that parasitic infection represents a major health impact on goats at New Valley with special reference to Eimeria spp. and Hemonchus contortus in both young and adults. The influence of seasonal variation proved higher coccidial infection at winter (86.7%), however higher intestinal helminths infection were found at spring and summer. It could be concluded that periodical parasitic examination of goats in NewValley should be attempted to recognize and manage parasitic infection.

 

Key words: Internal, parasite, goats, New Valley

 

Introduction

 

Internal parasites of goats are considered one of the biggest problems where it can cause major health issues, which have a major effect on the animal performance and causes great economic losses not due to mortality but due to production loss (Waller, 2004). The proper management of the internal parasites is extremely important to effectively reduce the herd exposure to parasites.

One of the first things that producer should realize, that goats are naturally browsers in contrast to sheep and cattle which are grazers. Additionally goats have traditionally been raised in dry-arid climate in extensive production systems and they simply have not had opportunity to adapt to the warm-moist condition of a humid climate. All of these factors in addition to the fact that many of the parasites that affect goats thrive in warm, moist condition and live close to the ground (Waller, 2004). Gastrointestinal nematode infection can be treated by anthelmintic chemotherapy; however, treatment costs and drug resistance has elevated in all major parasite species (Ross 1997, Zajac and Gipson 2000 and Veale 2002). Compared to sheep, which develop a strong natural immunity around 12 months of age, goats acquire a lower level of immunity to gastrointestinal parasites. This explain why goats having greater populations of adult parasites with high egg output. In experimental Teladorsagia (Ostertagia) circumcincta infection (Macaldowie et al. 2003) found that goats carried higher worm burden than lambs and there were significant differences in the stages of development attained by the larval challenge established in the two species. Mullerius capillaris was reported to cause Verminous bronchitis among goats causing sever losses (Bruce et al., 1986)

 

Materials and Methods

 

Animals (Table 1):

The study was carried out on 515 goats (different ages and sexes) of native breed from various regions of New-valley Governorates (300 goats from El-Kharga and 215 from El-Dakhla). In order to properly manage a herd, it is important to be able to recognize the signs of parasitism. Diagnosis is usually done by observing the clinical signs and performing a fecal egg count test.

A- Observing the clinical signs:

Diseased goats were usually isolated from the herd and do not eat normally. Daily visual inspection is usually sufficient to monitor for parasitic infection.

B- Other diagnostic methods such as a fecal egg counts must also be routinely done since the biggest impact of internal parasites occur in the sub clinical level (not easily detected by visual observation) (Waller and Thramsborg, 2004).

 

Sampling:

Fecal samples were collected directly from the rectum or immediately after defecation, then kept in clean plastic sac, labeled with the required data concerning age, sex, date of collection and any apparent clinical signs, then sent to the diagnostic laboratory.

 

Gross examination of samples:  

Fecal samples were grossly examined for color, consistency, presence of mucous, blood, indigested feed and parasites (intact parasite, and / or larvae or gravid segments of Cestodes (Charles 1998).

 

Parasitological examination:

Fecal samples were examined by using floatation technique in saturated NaCl solution for detection of Nematode and Cestode eggs (Burger and stoy, 1968) and sedimentation technique for detection of Trematode eggs (Charles 1998). Egg count was done by using McMaster counting slide (Seivwright et al., 2004 and Pereckienė et al., 2007)

 

Fecal culture:

In order to assess species of gastrointestinal nematodes, samples of feces from individual animals were cultured for third stage larval development (Christie and Jackson, 1982). After 7 days of incubation larvae from cultures were harvested and identified to genera or species using light microscope. Baermanُ s technique was used for detection of lung worm infection. Identification of the collected eggs and larvae was done according to Dunn, (1978) and Soulsby (1982).

 

Results

 

In the present study 515 goats with variable ages, sexes and seasons were selected from different localities in New Valley Governorate during the peried of one year, Table (1).

A- Observed clinical signs:

Some of the observable clinical signs of heavy internal parasite infection are anemia, bottle-jaw and wasting away or poor weight gain, anemia results from blood sucking parasites is clearly observed in scleral and oral mucus membranes.

B- Parasitological findings (Tables 2-5 and Fig. 1-4):

As many as 88.34% of examined goats were infected with at least one genus/species of parasite. In this study Eimeria infection was the most prevalent parasitic infection (78.02%) where its rate in young  < 1 year was 75% and 80% in adults. Helminthes infection was detected in 55.6% of totally examined goats with infection rates of 40.55 and 64.72 % in young and adult respectively (Table 2).

Strongyloid like eggs were the most predominant nematodes observed in the examined fecal samples (25.93%) but in fecal culture the most predominant worms were Hemonchus spp., Chabertia spp., Trichostrongylus spp., Ostertagia spp. and Oesphogastomum spp.  Their infection rate was 10.10, 5.93, 5. 49, 4.6, 3.07% respectively (Table 5).  Fasciola eggs (Trematode) were detected only in adult goats in ratio of 12.74% and Cestodes infection were detected in 3.95% of examined goats (Table 3). Rate of infection was higher in female (94.52%) than in males (79.02%) as in Table 6.

Concerning to the seasonal variation, the incidence of Eimeria   was the most prevalent parasitic infection allover the year, where it was ranged from (86.72%) in winter to (68.96%) in spring, but Nematode increase gradually at autumn and reach to the high level of infection in winter and spring but low level of infection indicated in summer    (Table 4).

 

 

Table 1:  The goats selected for the study.

 

               Items

Localities

No.

Sex

Age

Season

M

F

<1 Y

> 1 Y

Win

Spr.

Sum

Aut

 

 

 

El- Kharga

El-Monera

59

34

25

30

29

15

14

15

15

El-Thawra

47

20

27

17

30

11

11

13

12

Boulak

56

16

40

16

40

14

14

14

14

El-Rawad

60

20

40

18

42

15

15

15

15

Darb-El arbin

78

20

58

36

42

19

20

20

19

Total

300

110

190

117

183

74

74

77

75

El-Dakla

El –Hendaw

56

20

36

20

36

14

14

14

14

El-Rashda

48

10

38

26

22

12

12

12

12

El-Maashra

41

8

33

19

22

10

10

10

11

West-El Mowhoub

70

20

50

28

42

17

17

18

18

Total

215

58

157

93

122

53

53

54

55

 

Table 2: Prevalence of parasitic infection in examined goats in New – Valley Governorate.

 

    Item

 

Animals

No.

Infected animals

Single coccidian

Single helminth

Mixed infection

Total coccidia

Total helminth

N.

%

N.

%

N.

%

N.

%

N.

%

N.

%

< 1 Year

210

180

85.7

107

59.44

45

25

28

15.55

135

75

73

40.55

> 1 Year

305

275

90.6

97

35.27

55

20

123

44.72

220

80

178

64.72

Total

515

455

88.4

204

44.83

100

21.97

151

33.18

355

78.62

251

55.16

                  

Table 3: Prevalence of parasitic infection with relationship of age
in examined goats.

                  Items

 

Parasite                                

Young < 1year

N (180)

Adult

N (275)

Total

N (455)

N.

%

N.

%

N.

%

Nematodes:

  • Toxocara Vitulorum
  • MuelleriusCapillaris
  • Trichuris ovis
  • Strongyloids like eggs

 

5

2

8

48

 

2.77

1.11

4.44

26.66

 

-----

18

9

70

 

-----

6.54

3.27

25.4

 

5

20

17

118

 

1.09

4.93

3.73

25.9

Cestode.

   Monezia.spp.

 

5

 

2.77%

 

13

 

4.72

 

18

 

3.95

Trematode.

  • Fasciola spp.
  • Paramphistomum spp.

 

-

5

 

-------

2.77%

 

58

10

 

21.09

3.63

 

58

15

 

12.74

3.29

Protozoa.

      Eimera. spp.

 

135

 

75%

 

220

 

72.13%

 

355

 

78.02

Table 4:  Seasonal variation with different parasite in examined goats.

 

Parasitic Species

Summer

N (113)

Autumn

N (113)

Winter

N (113)

Spring

N (116)

N.

%

N.

%

N.

 %

N.

%

Nematades:

  • Toxocara.vitillorum
  • Muellerius capillaries.
  • Trichurs. ovis
  • Strongylidea like eggs
    1. H. contortus.
    2. Ostertagia.spp.
    3. Chabertia.
    4. Oesphogastomum

 

 -

  3

  -

   -

  5

  1

  -

  2

 

---

2.65

---

-

4.42 0.9

-----

 1.8

 

 1

 3

 2

 

10

6

5   5

 

0.9

2.65

1.76

-

8.84

5.3

4.42

4.42

 

  3

  7

  8

 20

 6 13

 5

--

 

2.65

6.2

7.07

-

17.69

5.3

11.5

4.42

 

  1

  5

  5

-

11

  8

  9

 2

 

0.9

4.3

4.3

-

9.5

6.9

7.8

4.3

Cestodes:  Moniezia.spp.

 3

2.7

4

3.5

2

1.8

9

7.8

Trematode:

  • Fasciola. spp.
  • Paramphistomum.spp.

 18

  -

-

15.9

 ---

  -  

16

  5 

-

14.2

 4.4

 20

  2

--

-

17.69

 1.8

-

15

11

-

12.9

9.5

Protozoa:  Eimeria.spp.

82

72.6

95

84.1

98

86.7

80

68.9

 

Table 5: Prevalence of helminthes detected by fecal culture
in examined goats.

 

Parasitic species

Young

N (180)

    Adult

   N (275)

        Total

Characteristic of infective larvae

N.

%

N.

%

N.

%

Trichostrongylus spp.

5

2.77

20

7.27

25

5.49

Short straight larva with small tubercle, conical tail sheath

Oesphogastomum spp.

4

2.22

10

3.63

14

3.07

Simple pointed long tail

Chabertia spp.

7

3.88

20

7.27

27

5.93

The larva has 32 rectangular intestinal cells

Hemonchus spp..

6

3.33

40

14.54

46

10.10

Head bullet-shaped and has pointed tail

Ostertagia spp.

-

-

21

7.63

21

4.6

Conical, finger like tail

 

Table 6: Prevalence of parasitic infection in relation to sex
of examined goats.

 

 Animals

Sex

No. of examined goats

Positive cases

No.

%

 

   Goats

 Females

310

293

94. 52%

  Males

205

162

79.o2%

  Total

515

455

88.34 %

Figures

 

 

     Fig. 1: Moniezia spp. eggs

 

 

     Fig. 2: Eimeria ovis

 

 

Fig. 3 : Fasciola spp. egg

Fig. 4: Muellerius capillaris larva

 

Discussion

 

The results of the present study supports the opinion that goats acquire a lower level of immunity to gastrointestinal parasites than other ruminant. The infection with Eimeria spp. (Coccidia) result in serious clinical signs of fluid diarrhea which may or may not contain mucus or blood, dehydration, weakness, loss of appetite and death while some goats may instead be constipated and suddenly die without diarrhea.

Coccidian parasites were detected in 90.3% at Saudi Arabia (Alyousif et al., 1992) and 94.65% of examined goats in Egypt (Otify, 1984). Eimeria oocyst are widly present in feces of both normal and diseased goats in a reported range of 38% to 100% of all goats (Smith and Sherman, 1994). One of the most prevalent infection of Trichostrongyloid nematodes was Hemonchus Contortus (blood sucking worm) and Muellerius capillaries which is associated with marked tissue damage and pronounced cellular reaction. These results agreed with Berrag et al. (1997).

Bottle-jaw in gastrointestinal parasite infection is caused by hypoalbuminemia that results from either decreased feed intake, lack of appetite and increase the demands of proteins (Ashraf and Nepote 1990 and Min et al., 2005).  The absence of Fasciola infection in young goats agree with the same result of (El–Sherif and Abo-EL- Hadid, 2005 and Mohsen and Ibrahim., 2008). Concerning the relationship between the sexes of examined goats and the infection rate, females were highly infected than males and this may be attributed to the fact that females are exposed to more stress like, pregnancy, lactation and parturition. These results agreed with those of Abd el- Wahed (1987).

Concerning the seasonal dynamics of parasitic helminthes infection, the study revealed that the incidence of nematode increase gradually at autumn and reach to the peak in winter and spring, but low level of infection observed in summer. This pattern may be attributed to the spring rise phenomena but the infective stage of most Strongyloid worm not resist the hot dry season. This phenomena mentioned  by Herd (1971) as the end of winter and beginning of spring is considered as the peak of reproduction and  maturation of their inhibited larvae takes place in spring season which known as spring rise.

 

References

 

Abd El-Wahed, M.M. (1987):  Morphological studies on gastrointestinal nematode infesting buffaloes in Kalubia and Sharkia Governorate. M. V. Sc. Thesis, CairoUniversity.

Alyousif, M.S.; Kasim, A.A. and Shawa, Y.R. (1992): Coccidiosis in domestic goats (Cabrahiricus) in Saudi Arabia. Inter. J. Parasitology, 22 (6) 807-811.

Ashraf, M. and Nepote, K.H. (1990): Prevalence of gastrointestinal nematodes, coccidian and lung worms in Maryland dairy goats. Small Ruminant Research, 3, 291-298.

Berrag, B.; Rhalem, A.; Sahibi, H.; Dorchies, P. and Cabaret, J. (1997):  Bronchoalveolar cellular responses of goats Following infections with Muellerius Capillaris (Protostrongylidae Nematode). Veterinary immunology and immunopathology, 58, 77-88.

Bruce, M. McCraw and Paula, I. Menzies (1986):  Treatment of Goats Infected with the Lungworm Muellerius capillaries. Can Vet. J.; 27(8): 287–290

Burger, H.J. and Stoy, M. (1968):  Parasitologische diagnostic (Teil 11) Elzahlung und larven differeniekung. Therapogen praxid dienst, 3, 1-22.

Charles, M. (1998): Diagnostic veterinary parasitology, second Edition, page 245-254.

Christie, M. and Jackson, F. (1982): Specific identification of strongyle egg in small samples of sheep feces. Research in Veterinary Science, 32, 113-117.

Dunn, A.M. (1978): Veterinary Helminthelogy.2nd Ed. Butter and Tanner lid, frome and Landon. Pp. 295-304.

El sheriff, A.M. and Abo-El Hadid, S.M. (2005): Episoatiological investigation about different internal parasitic affection among cattle calves in Beni-Suef Governorate. J. Egypt. Vet. Med. Ass., 65 (6) 261-274.

Herd, R.P. (1971): The parasitic life cycle of Chabertia ovina in sheep.
Internal J. Parasitology, 1, 189-199.

Macaldowie, C.; Jackson, F.; Huntley, J.; Mackellar, A. and Jackson, E. (2003): A comparison of larval development and mucosal mast cell responses in worm-naïve goat yearlings, kids and lambs undergoing primary and secondary challenge with Teladorsagia circumcincta. Veterinary parasitology, 114, 1-13.

Min, B.R.; Hart, S.P.; Miller, D.; Tomita, G.M.; Loetz, E. and Sahlu, (2005): The effect of grazing forage containing condensed Tannis on gastrointestinal parasite infection and milk composition in Angoro does. Veterinary Parasitology, 130, 105-113.

Mohsen, I.A. and Ibrahim, A. (2008): Studies on some internal parasites of goats in Assiut Governorate especially which affecting liver. AssiutUniversity. Bull. Environmental Research, 11: (1)      57-71.

Otify, Y.Z. (1984): Studies on Coccidian parasites of goats.
Ph. D. Fac. Vet. Med. Alex. University.

Pereckienė, A.; Kaziūnaitė, V.; Vyšniauskas, A.; Petkevičius, S.; Malakauskas, A.; Šarkūnas, M. and Taylor, M.A. (2007): A comparison of modifications of the McMaster method for the enumeration of Ascaris suum eggs in pig faecal samples Veterinary Parasitology Volume 149, Issues 1-2, Pages 111-116.

Roos, M.H. (1997): The role of drug in the control of parasitic nematode infections, must we do without parasitology, 114, 137-144.

Seivwright, L.J.; Redpatha.1 , S.M.;  Mougeot, F.; Watt. L. and Hudson,   P.J. (2004): Faecal egg counts provide a reliable measure of Trichostrongylus tenuis intensities in free-living red grouse Lagopus lagopus scoticus. Journal of Helminthology, 78: 69-76 Cambridge University Press doi:10.1079/JOH2003220 Published online by Cambridge University Press 22 Feb 2007

Smith, M.C. and Sherman, D.M. (1994): Goat Medicine 1st Ed. Lea Febiger U.S.A. page 312-340.

Soulsby, E.J.L. (1982): Helminths, Arthropods and Protozoa of domesticate animals 7th Ed. The English Language Book. Society and Baillier Tindall, London. Pp 795-803.

Veale, P.I. (2002): Resistance to macrocytic lactones in nematodes of goats. Australian Veterinary J., 80, 303-304.

Waller, P.S. (2004): Management and control of nematode parasites of small ruminants in the face of total anthelmintic failure. Tropical biomedicine, 21, 7-13.

Waller, P.S. and Thramborg, S.M. (2004): Nematode control in green ruminant production systems. Trends in Parasitology. 20 (10) 493-497.

Zajac, A.M. and Gipson, T.A. (2000): Multiple anthelmintic resistance in a goat herd. Vetrinary Parasitology, 87, 163-172.

 

 

 

 

 

 

 

 

 

 
Abd El-Wahed, M.M. (1987):  Morphological studies on gastrointestinal nematode infesting buffaloes in Kalubia and Sharkia Governorate. M. V. Sc. Thesis, CairoUniversity.
Alyousif, M.S.; Kasim, A.A. and Shawa, Y.R. (1992): Coccidiosis in domestic goats (Cabrahiricus) in Saudi Arabia. Inter. J. Parasitology, 22 (6) 807-811.
Ashraf, M. and Nepote, K.H. (1990): Prevalence of gastrointestinal nematodes, coccidian and lung worms in Maryland dairy goats. Small Ruminant Research, 3, 291-298.
Berrag, B.; Rhalem, A.; Sahibi, H.; Dorchies, P. and Cabaret, J. (1997):  Bronchoalveolar cellular responses of goats Following infections with Muellerius Capillaris (Protostrongylidae Nematode). Veterinary immunology and immunopathology, 58, 77-88.
Bruce, M. McCraw and Paula, I. Menzies (1986):  Treatment of Goats Infected with the Lungworm Muellerius capillaries. Can Vet. J.; 27(8): 287–290
Burger, H.J. and Stoy, M. (1968):  Parasitologische diagnostic (Teil 11) Elzahlung und larven differeniekung. Therapogen praxid dienst, 3, 1-22.
Charles, M. (1998): Diagnostic veterinary parasitology, second Edition, page 245-254.
Christie, M. and Jackson, F. (1982): Specific identification of strongyle egg in small samples of sheep feces. Research in Veterinary Science, 32, 113-117.
Dunn, A.M. (1978): Veterinary Helminthelogy.2nd Ed. Butter and Tanner lid, frome and Landon. Pp. 295-304.
El sheriff, A.M. and Abo-El Hadid, S.M. (2005): Episoatiological investigation about different internal parasitic affection among cattle calves in Beni-Suef Governorate. J. Egypt. Vet. Med. Ass., 65 (6) 261-274.
Herd, R.P. (1971): The parasitic life cycle of Chabertia ovina in sheep.
Internal J. Parasitology, 1, 189-199.
Macaldowie, C.; Jackson, F.; Huntley, J.; Mackellar, A. and Jackson, E. (2003): A comparison of larval development and mucosal mast cell responses in worm-naïve goat yearlings, kids and lambs undergoing primary and secondary challenge with Teladorsagia circumcincta. Veterinary parasitology, 114, 1-13.
Min, B.R.; Hart, S.P.; Miller, D.; Tomita, G.M.; Loetz, E. and Sahlu, (2005): The effect of grazing forage containing condensed Tannis on gastrointestinal parasite infection and milk composition in Angoro does. Veterinary Parasitology, 130, 105-113.
Mohsen, I.A. and Ibrahim, A. (2008): Studies on some internal parasites of goats in Assiut Governorate especially which affecting liver. AssiutUniversity. Bull. Environmental Research, 11: (1)      57-71.
Otify, Y.Z. (1984): Studies on Coccidian parasites of goats.
Ph. D. Fac. Vet. Med. Alex. University.
Pereckienė, A.; Kaziūnaitė, V.; Vyšniauskas, A.; Petkevičius, S.; Malakauskas, A.; Šarkūnas, M. and Taylor, M.A. (2007): A comparison of modifications of the McMaster method for the enumeration of Ascaris suum eggs in pig faecal samples Veterinary Parasitology Volume 149, Issues 1-2, Pages 111-116.
Roos, M.H. (1997): The role of drug in the control of parasitic nematode infections, must we do without parasitology, 114, 137-144.
Seivwright, L.J.; Redpatha.1 , S.M.;  Mougeot, F.; Watt. L. and Hudson,   P.J. (2004): Faecal egg counts provide a reliable measure of Trichostrongylus tenuis intensities in free-living red grouse Lagopus lagopus scoticus. Journal of Helminthology, 78: 69-76 Cambridge University Press doi:10.1079/JOH2003220 Published online by Cambridge University Press 22 Feb 2007
Smith, M.C. and Sherman, D.M. (1994): Goat Medicine 1st Ed. Lea Febiger U.S.A. page 312-340.
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