IMPORTANCE OF APPLICATION OF SOME ENVIRONMENTAL MEASURES AFTER DEWORMING OF STRAY DOGS INFECTED WITH SOME HELMINTH PARASITES

Authors

1 Dept. of Parasitology, Fac. of Vet. Med., Beni-Suef Univ.

2 Medical Biochemistry Unit, Animal Health Research Institute, Dokki, Giza

Abstract

The present study showed that treatment of stray dogs in captivity in order to prepare them for further experimental infection is not enough for elimination of parasites previously recorded in them. This phenomenon is not only related to the efficacy of the drugs used, but also for complete disinfection of places of captivity against infective stages of all included parasites. This study clears that after treatment of 2 groups of stray dogs captive in separate boxes by using Praziquantil      (1 Tablet/5-7kg B.W) and Fenbendazole (50 mg/kg B.W) revealed complete disappearance of Taenia sp. and Dipylidium caninum            (D. caninum) eggs and their gravid segments. Fenbendazole led to disappearance of previously diagnosed Ancylostoma caninum              (A. caninum) and Toxocara canis (T. canis) eggs at 2 weeks post treatment. Re-examination of captive dogs in floor pin 6 weeks post treatment revealed presence of T. canis, A. caninum, Taenia sp. and      D. caninum eggs by percentages of 9.09, 3.03, 6.06 and 6.06 % respectively in animals more than one year; while those less than one year showed incidence of T. canis, Taenia sp. and D. caninum with percentages of 16.67, 8.33 and 8.33 % respectively. On the other hand, re-examination of captive dogs in metal battery 6 weeks post treatment proved that there was no infection among them. This means that          re-infection took place as a result of the presence of intermediate host of    D. caninum, while reappearance of A. caninum and T. canis may be related to the presence of infective stages contaminating the media surrounding the treated dogs or presence of some migrating larvae that succeeded to escape from the applied treatment. This clears that the previous contamination in these boxes and their surroundings plays an important role in the re-infection of these animals by some parasites especially those depending on arthropod-intermediate hosts or those did not need intermediate hosts. In conclusion, this study denotes the importance of application of restricted measures to these boxes and their surrounding places together with prevention of arrival of other stray animals as well as rodents to these habitats.
 

Keywords


Dept. of Parasitology,

Fac. of Vet. Med., Beni-SuefUniv.

 

Importance of application of some environmental measures after deworming of stray dogs infected with some helminth parasites    

 

(With One Table)

 

By

Kh.M. El-Dakhly and Ragaa A. Soliman*

* Medical Biochemistry Unit, Animal Health Research Institute, Dokki, Giza

(Received at 15/9/2008)

 

أهمية تطبيق بعض الاشتراطات البيئية بعد علاج الکلاب الضالة المصابة ببعض الديدان المتطفلة

 

 خالد محمد الداخلي ، رجاء عبد الستار سليمان

 

تبين من هذه الدراسة أن علاج الکلاب الضالة والتي تم حبسها بغرض تجهيزها لإحداث عدوى تجريبية ليس کافيا للتخلص من الطفيليات الموجودة بها. وتعزى هذه الظاهرة إلى کل من کفاءة العقار المستخدم بالإضافة إلى التطهير الکامل لأماکن حبس هذه الکلاب ضد الأطوار المعدية لکل الطفيليات الموجودة. وفي هذه الدراسة تم علاج مجموعتين حبيستين من الکلاب باستخدام عقاري البرازيکونتيل (قرص/5-7 کجم من وزن الجسم) والفيبندازول (50 مجم/کجم من وزن الجسم) مما نتج عنه التخلص الکامل من کل البويضات والقطع الحاملة لکل من دودة التينيا ودودة الکلب الشريطية کما أدى استخدام عقار الفيبندازول إلى التخلص من کل من دودة الکلب الخطافية ودودة اسکارس الکلاب وذلک بعد أسبوعين من استخدام العقار. وقد بينت إعادة فحص نفس الکلاب بعد ستة أسابيع من العلاج ظهور بويضات اسکارس الکلاب ودودة الکلب الخطافية ودودة التينيا ودودة الکلب الشريطية بنسب 9.09، 3.03، 6.06 ، 6.06 % على الترتيب وذلک في الحيوانات التي تزيد أعمارها عن عام واحد, في حين کانت نسب الإصابة 16.67، صفر، 8.33، 8.33 % على الترتيب في الحيوانات التي تقل أعمارها عن عام مما يعنى حدوث تکرار للعدوى بسبب وجود العوائل الوسيطة لبعض الديدان مثل دودة الکلب الشريطية أو وجود الأطوار المعدية لبعض الديدان في الوسط المحيط بالکلاب أو حتى وجود بعض اليرقات النشطة والتي لم يؤثر العقار عليها کما في بعض الديدان مثل دودة الکلب الخطافية ودودة اسکارس الکلاب. وهذا يشير إلى أن تلوث صناديق تربية الکلاب والوسط المحيط بها يلعب دورا هاما في حدوث العدوى مرة أخرى بالطفيليات الموجودة وخاصة تلک التي تعتمد منها على وجود الحشرات کعائل وسيط أو حتى التي لا تحتاج إلى عوائل وسيطة. ونستخلص من هذه الدراسة أهمية تطبيق الأشتراطات الصحية علي أماکن تربية هذه الحيوانات وکذلک البيئة المحيطة بها مع محاولة منع وصول أي حيوانات أخري ضالة أو قوارض إلي هذه الأماکن.

 

SUMMARY

 

The present study showed that treatment of stray dogs in captivity in order to prepare them for further experimental infection is not enough for elimination of parasites previously recorded in them. This phenomenon is not only related to the efficacy of the drugs used, but also for complete disinfection of places of captivity against infective stages of all included parasites. This study clears that after treatment of 2 groups of stray dogs captive in separate boxes by using Praziquantil      (1 Tablet/5-7kg B.W) and Fenbendazole (50 mg/kg B.W) revealed complete disappearance of Taenia sp. and Dipylidium caninum            (D. caninum) eggs and their gravid segments. Fenbendazole led to disappearance of previously diagnosed Ancylostoma caninum              (A. caninum) and Toxocara canis (T. canis) eggs at 2 weeks post treatment. Re-examination of captive dogs in floor pin 6 weeks post treatment revealed presence of T. canis, A. caninum, Taenia sp. and      D. caninum eggs by percentages of 9.09, 3.03, 6.06 and 6.06 % respectively in animals more than one year; while those less than one year showed incidence of T. canis, Taenia sp. and D. caninum with percentages of 16.67, 8.33 and 8.33 % respectively. On the other hand, re-examination of captive dogs in metal battery 6 weeks post treatment proved that there was no infection among them. This means that          re-infection took place as a result of the presence of intermediate host of    D. caninum, while reappearance of A. caninum and T. canis may be related to the presence of infective stages contaminating the media surrounding the treated dogs or presence of some migrating larvae that succeeded to escape from the applied treatment. This clears that the previous contamination in these boxes and their surroundings plays an important role in the re-infection of these animals by some parasites especially those depending on arthropod-intermediate hosts or those did not need intermediate hosts. In conclusion, this study denotes the importance of application of restricted measures to these boxes and their surrounding places together with prevention of arrival of other stray animals as well as rodents to these habitats.

 

Key words: Helminth parasites, Toxocara, Dipylidium, Anclystoma,       Taenia, dog.

Introduction

 

Gastrointestinal parasites are among the most common pathogenic agents encountered by veterinarians dedicated to companion animals and they constitute one of the main causes of pathological lesions in alimentary tract of dogs (Ramirez-Barrios et al., 2004).

Control of these parasites is usually based on using of anthelmintic prophylaxis, so, to obtain a regular deworming, periodic examination of fecal samples and treatment of the infected dogs must be involved (Emde, 1993 and Pullola et al., 2006).

The care of animals has always included the management of internal parasites. As technology has progressed, the medications developed have become more and more broad in the spectrum of parasites they can eradicate. Several researches applied on dogs depending on collection of small numbers of stray dogs of different ages in small boxes and treatment of their natural infection before starting the original experimental trials especially those of parasitic studies. Several number of helminthes are common in dogs required arthropods intermediate hosts including Dipylidium caninum (Wang et al., 2006), also others as Toxocara canis and Ancylostoma caninum (Epe et al., 1996)and did not need intermediate host, where they can still contaminate the boxes underneath the animal. These infective larvae can resist the adverse conditions and survive for longer times (Bugg,1999). Large numbers of these parasites have zoonotic importance and can pollute the conditions surrounding the human beings and other animals (Martinez-Moreno et al., 2007). Even with application of a restricted control measures to these boxes, arrival of rodents and other stray animals as cats can be considered a source of infection for these places even after application of repeated treatment programs (Pullola et al., 2006).

Helminthes infection of these dogs commonly occurs per os while others are more common infecting dogs prenatally or via milk as T. canis. These parasites cause cough, pneumonia, restlessness and anaemia for infected dogs (Parsons et al., 1986).

Treatment of these animals is considered as one of the fastest ways for eradication of these parasites, but without complete eradication to the source of re-infection of these animals is still considered as a source for new infection and spreading of the disease (Thompson and Roberts, 2001).

The present study spot more light on types of parasites infecting stray and captive dogs under hygienically different conditions in separate boxes in Beni-Suef Governorate, Egypt. Source of re-infection by some parasites post specific treatment and the requirement for prevention of this was also evaluated. The present work aims to minimize the role of these animals as a source of dangerous diseases preventing them from acting as infectious foci for their surrounding animals and human beings under the common medium to low hygienic precautions.   

 

Materials and Methods

 

I- Selection and grouping of animals:

 

            A total number of 200 stray dogs (140 more than one year and 60 lower than one year) taken from Sharq El-Nile area, Beni-Suef, Egypt were examined during this investigation. Fecal samples of these animals were examined by using sedimentation and floatation techniques according to Soulsby (1982).  

 

II- Treatment of infected animals:

The dogs infected with helminth parasites were treated with Fenbendazole (PanacurÒ) which is broad spectrum anthelmintic (50 mg/kg body weight once a day for 3 consecutive days as described by producer) used in dogs for elimination of gastrointestinal parasites (Thompson and Roberts, 2001).

 

Also, Praziquantel (DroncitÒ) is indicated for the removal of Dipylidium caninum, Taenia sp. and flukes. The recommended dosage of praziquantel varies according to body weight. Smaller animals require a relatively larger dosage because of their higher metabolic rate. The drug was given in a dosage of one tablet/5-7kg B.W. The medication was given, for each animal, via stomach tube to ensure that all animals received the proper dosage according to their weights in order to reach the full effectiveness of the dewormer therapy.

 

Four weeks after treatment, these dogs were divided into 2 equal groups; the first is kept in floor pin (1.5 x 1.5 m concrete floor pin with wire door), while the other is kept in a metal battery (60 x 60 x 60 cm). The treated dogs in the 2 groups were examined 2 weeks later.

For examination of reinfection, fecal samples were collected from all animals at days –7, zero, 7, 14, 21, 28, 35, and 42 days post treatment.

 

Results

 

            Examination of fecal samples of 140 dogs more than one year and 60 dogs less than one year revealed that number of infected dogs by helminth parasites was 33 (23.6 %) in dogs more than one year and      12 (20.0 %) in those less than one year.

 

            Table (1) illustrated that dogs more than one year were found to be infected with T. canis, A. caninum, Taenia sp., D. caninum and        H. heterophyes eggs with percentages of 10.0, 5.0, 2.9, 3.6 and 2.1 % respectively. On the other hand, it was found that the examined dogs less than one year were infected with T. canis, A. caninum, Taenia sp. and   D. caninum eggs with percentages of 10.0, 5.0, 3.3 and 1.7 % respectively.

 

            Four weeks after treatment of the 2 groups of stray dogs captive in separate boxes by using Praziquantil and Fenbendazole, it was found that stray dogs captive in floor pin were found to be still infected with helminth parasites, where the fecal examination of the captive stray dogs in floor pin revealed that 11 (33.33 %) dogs more than one year were found to be infected; showing 3 (9.09 %) cases were infected with        T. canis, one dog (3.03 %) was found to be infected with A. caninum, while 2 dogs (6.06 %) were found to be still infected with D. caninum. Also, 2 cases (6.06 %) were still infected with Taenia sp. eggs. On the other hand, it was evident that, 5 dogs (41.67 %) less than one year were found to be still infected 4 weeks post treatment; where 2 cases (16.67 %) were found to be infected with T. canis and one dog (8.33 %) was found to be infected with both Taenia sp. and D. caninum.

 

            Examination of captive stray dogs in metal battery 4 weeks post treatment revealed that there was no parasitic infection could be detected in fecal samples which examined 3, 4, 5 and 6 weeks post treatment.

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

Discussion

 

            The present investigation was designed to confirm that treatment of stray dogs in captivity in order to prepare them for further experimental infections is not enough for elimination of parasites previously recorded in them.

            This phenomenon is not only related to the efficacy of the drugs used, but also to the complete disinfection of places of captivity against infective stages of all included parasites (Dalimi et al., 2006).

            The present investigation showed that using of metal battery post treatment was found to be more better than floor pin, where it was revealed that the efficacy of the drug used was not sufficient to eliminate the helminthes, but the complete disinfection of places of captivity against infective stages is much necessary to keep the dogs post treatment free from parasites (Thompson and Roberts, 2001).

            Our results go parallel with those obtained by Smith et al. (1980) and Mousa et al. (2001). In addition, Romero (1999); Eguia-Aguilar     et al. (2005) and Wang et al. (2006) found that several numbers of helminthes common in dogs required arthropod intermediate hosts including D. caninum. Also, others as T. canis and A. caninum did not need intermediate hosts, where they still contaminate the boxes underneath the animals.

            The fact which in agreement with our results was evident from the experiment that the captivity of the stray dogs in metal battery is more better than the captivity of dogs post treatment in the floor pin. The results which are obvious in the present study, are that the treated dogs kept in floor pin were found to be still infected with helminth parasites 4 weeks post treatment, while the treated dogs kept in metal battery were found to be free from helminth parasites (Habluetzel et al., 2003; Pullola et al., 2006 and Martinez-Moreno et al., 2007).   

 

References

 

Bugg, R.J. (1999): Gastrointestinal parasites of urban dogs in Perth, Western Australia. Vet. J., 157: 295–301.

Dalimi, A.; Sattari, A. and Motamedi, Gh. (2006): A study on intestinal helminthes of dogs, foxes and jackals in the western part of Iran. Vet. Parasitol., 142: 129–133.

 

Eguia-Aguilar, P.; Cruz-Reyes, A. and Martinez-Maya, J.J. (2005): Ecological analysis and description of the intestinal helminthes present in dogs in Mexico City. Vet. Parasitol., 127 (2):      139–146.

Emde, C. (1993): Untersuchungen zur Resistenz Von Toxocara canis bzw. Toxocara cati gegen Anthelmintika. Der. Prakt. Tierarzt., 9: 811–822.

Epe, C.; Schnieder, T. and Stoye, M. (1996): Moglichkeiten un Grenzen der chemotherapeutischen Bekampfung vertikler Infektionen mit Toxocara canis und Ancylostoma caninum beim Hund. Der. Prakt. Tierarzt., 6: 483–489.

Habluetzel, A.; Traldi, G.; Ruggieri, S.; Attili, A.R.; Scuppa, P.; Marchetti, R.; Menghini, G. and Esposito, F. (2003): An estimation of Toxocara canis prevalence in dogs, environmental eggs contamination and risk of human infection in the Marche region of Italy. Vet. Parasitol., 113: 243-252.

Martinez-Moreno, F.J.; Hernandez, S.; Lopez-Cobos, E.; Becerra, C.; Acosta, I. and Martinez-Moreno, A. (2007):Estimation of canine intestinal parasites in Cordoba (Spain) and their risk to public health. Vet. Parasitol., 143 (1): 7–13.  

Mousa, W.M.; Ezz El-Dien, N.M. and Fouad, S. (2001): Evaluation of three Toxocara canis antigens for serodiagnosis of experimentally infected rabbits with visceral larva migrans. J. Egypt. Vet. Med. Ass., 61 (1): 173–180. 

Parsons, J.C.; Bowman, D.D. and Grieve, R.B. (1986): Tissue localization of excretory-secretory antigens of larval Toxocara canis in acute and chronic murine toxocariasis. Am. J. Trop. Med. Hyg., 35 (5): 974–981.   

Pullola, T.; Viermaa, J.; Saari, S.; Virtala, A.M.; Nikander, S. and Sukura, A. (2006):Canine intestinal helminthes in Finland: Prevalence, risk factors and endoparasite control practices. Vet. Parasitol., 140 (3-4): 321–326.

Ramirez-Barrios, R.A.; Barboza-Mena, G.; Munoz, J.; Hernandez, E.; Gonzalez, F. and Escalona, F. (2004):Prevalence of intestinal parasites in dogs under veterinary care in Malacaibo, Venezuela. Vet. Parasitol., 121: 11–20.

Romero, C.E. (1999): Frecuencia de parasitos intestinales en perros del DF., AMVEPE: 27–29.

 

Smith, H.V.; Quinn, R.; Bruce, R.G. and Girdwood, R.W. (1980): A paper radioimmunosorbent test (PRIST) for the detection of larva specific antibodies to T. canis in human sera. J. Immunol. Methods., 37: 47–55.

Soulsby, E.J. (1982): Helminthes, Arthropoda and Protozoa of domesticated animals. 7th ed. Bailliere Tindal & Casell Ltd. London.

Thompson, A.R. and Roberts, M.G. (2001): Does pet helminth prophylaxis increase the rate of selection of drug resistance ?. Trends in Parasitol., 17 (12): 576–578.

Wang, C.R.; Qui, J.H.; Zhao, J.P.; Xu, L.M.; Yu, W.C. and Zhu, X.Q. (2006): Prevalence of helminthes in adult dogs in HeilongjiangProvince, the PeopleRepublic of China. Parasitol. Res., 99 (5): 627–630.

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 


Table 1: Prevalence of different helminth parasites recorded in the examined stray dogs before and after treatment under different environmental conditions.

 

 

Examined No.

Infected

Toxocara canis

Ancylostoma caninum

Taenia spp.

Dipylidium caninum

Heterophyes heterophyes

No.

%

No.

%

No.

%

No.

%

No.

%

No.

%

Before treatment

› one year

140

33

23.6

14

10.0

7

5.0

4

2.9

5

3.6

3

2.1

‹ one year

60

12

20.0

6

10.0

3

5.0

2

3.3

1

1.7

-

-

After treatment

Floor pin

› one year

70

11

33.33

3

9.09

1

3.03

2

6.06

2

6.06

-

-

‹ one year

30

5

41.67

2

16.67

­-

-

1

8.33

1

8.33

-

-

Metal battery

› one year

70

-

-

-

-

-

-

-

-

-

-

-

-

‹ one year

30

-

-

-

-

-

-

-

-

-

-

-

-


 

 
References
 
Bugg, R.J. (1999): Gastrointestinal parasites of urban dogs in Perth, Western Australia. Vet. J., 157: 295–301.
Dalimi, A.; Sattari, A. and Motamedi, Gh. (2006): A study on intestinal helminthes of dogs, foxes and jackals in the western part of Iran. Vet. Parasitol., 142: 129–133.
 
Eguia-Aguilar, P.; Cruz-Reyes, A. and Martinez-Maya, J.J. (2005): Ecological analysis and description of the intestinal helminthes present in dogs in Mexico City. Vet. Parasitol., 127 (2):      139–146.
Emde, C. (1993): Untersuchungen zur Resistenz Von Toxocara canis bzw. Toxocara cati gegen Anthelmintika. Der. Prakt. Tierarzt., 9: 811–822.
Epe, C.; Schnieder, T. and Stoye, M. (1996): Moglichkeiten un Grenzen der chemotherapeutischen Bekampfung vertikler Infektionen mit Toxocara canis und Ancylostoma caninum beim Hund. Der. Prakt. Tierarzt., 6: 483–489.
Habluetzel, A.; Traldi, G.; Ruggieri, S.; Attili, A.R.; Scuppa, P.; Marchetti, R.; Menghini, G. and Esposito, F. (2003): An estimation of Toxocara canis prevalence in dogs, environmental eggs contamination and risk of human infection in the Marche region of Italy. Vet. Parasitol., 113: 243-252.
Martinez-Moreno, F.J.; Hernandez, S.; Lopez-Cobos, E.; Becerra, C.; Acosta, I. and Martinez-Moreno, A. (2007):Estimation of canine intestinal parasites in Cordoba (Spain) and their risk to public health. Vet. Parasitol., 143 (1): 7–13.  
Mousa, W.M.; Ezz El-Dien, N.M. and Fouad, S. (2001): Evaluation of three Toxocara canis antigens for serodiagnosis of experimentally infected rabbits with visceral larva migrans. J. Egypt. Vet. Med. Ass., 61 (1): 173–180. 
Parsons, J.C.; Bowman, D.D. and Grieve, R.B. (1986): Tissue localization of excretory-secretory antigens of larval Toxocara canis in acute and chronic murine toxocariasis. Am. J. Trop. Med. Hyg., 35 (5): 974–981.   
Pullola, T.; Viermaa, J.; Saari, S.; Virtala, A.M.; Nikander, S. and Sukura, A. (2006):Canine intestinal helminthes in Finland: Prevalence, risk factors and endoparasite control practices. Vet. Parasitol., 140 (3-4): 321–326.
Ramirez-Barrios, R.A.; Barboza-Mena, G.; Munoz, J.; Hernandez, E.; Gonzalez, F. and Escalona, F. (2004):Prevalence of intestinal parasites in dogs under veterinary care in Malacaibo, Venezuela. Vet. Parasitol., 121: 11–20.
Romero, C.E. (1999): Frecuencia de parasitos intestinales en perros del DF., AMVEPE: 27–29.
 
Smith, H.V.; Quinn, R.; Bruce, R.G. and Girdwood, R.W. (1980): A paper radioimmunosorbent test (PRIST) for the detection of larva specific antibodies to T. canis in human sera. J. Immunol. Methods., 37: 47–55.
Soulsby, E.J. (1982): Helminthes, Arthropoda and Protozoa of domesticated animals. 7th ed. Bailliere Tindal & Casell Ltd. London.
Thompson, A.R. and Roberts, M.G. (2001): Does pet helminth prophylaxis increase the rate of selection of drug resistance ?. Trends in Parasitol., 17 (12): 576–578.
Wang, C.R.; Qui, J.H.; Zhao, J.P.; Xu, L.M.; Yu, W.C. and Zhu, X.Q. (2006): Prevalence of helminthes in adult dogs in HeilongjiangProvince, the PeopleRepublic of China. Parasitol. Res., 99 (5): 627–630.