ResearchersLinks

Case Report · Volume 4, Issue 3, 6 September 2016 · Open Access

Strategic Management of a Clinical Case of Recurrent Caseaous Lymphadenitis in a Goat Farm

· · · · · · · · · · ·

Article Info ⌄
Journal:
Research Journal for Veterinary Practitioners
Published:
6 September 2016

From the article

  • The clinical management of CLA revolves around early detection of the disease in a herd and culling of infected animals showing clinical manifestation of the disease.
  • CLA disease causes significant economic loss to small ruminant industry, therefore, it is important to design measures that will aim at reducing the rate of spread of the disease.
  • Because CLA is a disease of great economic and zoonotic importance, there is the need to design an effective strategic plan for its control and eradication in areas where the disease is endemic.
  • This clinical case showed the importance of effective implementation of vaccination strategies and other control measures in the control and prevention of CLA in small ruminants and its zoonotic implications in humans.

Selected from the article's own text.

Abstract

Faez Firdaus Abdullah Jesse1*, Asinamai Athliamai Bitrus2, Yusuf Abba2, Eric Lim Teik Chung1, Muhammad Abubakar Sadiq1, Idris Umar Hambali1, Heshini Perera1, Abd Wahid Haron1, Mohd Azmi Mohd Lila2, Abdul Aziz Saharee1, Mohd Jefri Norsidin1, Azrol Harith1

1Department of Veterinary Clinical Studies, Faculty of Veterinary Medicine, Universiti Putra Malaysia, 43400 Serdang, Selangor, Malaysia; 2Department of Veterinary Pathology and Microbiology, Faculty of Veterinary Medicine, Universiti Putra Malaysia, 43400 Serdang, Selangor, Malaysia.

Abstract | This clinical case describes the strategic management of a recurrent caseous lymphadenitis (CLA) in a goat farm. A 3 year old Saanen cross doe was presented with a history of a firm round swelling on the ventral side of the mandible. The goat farm had previous history of CLA three years ago. Blood and serum analysis showed that the doe had leukocytosis, neutrophilia with a left shift and monocytosis. Bacterial culture of the caseaous exudate revealed positive growth for Corynebacterium paratuberculosis. Further clinical examination in the farm revealed that two other goats were infected. To prevent further reinfection, the infected animals were culled. The findings of this clinical case necessitate the need for the adoption of effective biosecurity measures and thorough screening of animals before introducing them into flocks. 
 
Keywords | Caseaous lymphadenitis, Corynebacterium paratuberculosis, Doe, Management

Case History

Case Presentation

A 3 year old female Saanen cross doe was presented to the University Veterinary Hospital, Universiti Putra Malaysia with the complaint of swelling on the lower right mandible, which was first noticed three weeks prior to presentation. Clinical history revealed that the farm previously had CLA and was depopulated in 2008 in order to reduce the risk of spread of the disease. However, it was observed that the disease reoccurred after three years.

Physical Examination

Physical examination revealed a round firm, non-movable and non-painful mass on the ventral side of the mandible and an enlarged sub mandibular lymph node which was 1.5 x 1.5 centimeter in size (Figure 1). Vital parameters revealed that the doe had rectal temperature of 39.2 ºC, respiratory rate of 36 cycles per minute and pulse rate 72 beats per minute, respectively.

Diagnostic Work Plan

The swollen area was aseptically prepared and fine needle aspiration biopsy was attempted; however, there a caseaous exudate oozed out immediately the needle was removed (Figure 2). The exudate was collected in a plain tube for bacterial culture and identification while blood sample was collected for complete blood count and serum biochemistry. The result of the bacterial culture revealed a heavy growth of Corynebacteria pseudotuberculosis, while complete blood count showed leukocytosis and neutrophilia with a regenerative left shift and monocytosis thus, suggestive of an ongoing inflammatory process.

Figure 2: Excised Caseaous exudate and fine needle aspiration biops

Treatment Plan

The doe and other two showing clinical manifestation of CLA were culled in order to limit the spread of the disease to other healthy animals in the farm.

Discussions

Caseaous lymphadenitis (CLA) continues to pose a serious problem to the small animal industries, thus limiting their economic profitability. It has been observed that the sustained marketing and movement of small ruminants from one country to the other without the use of adequate biosecurity measures greatly limit the control and prevention of CLA . Thus, maintaining the prevalence of CLA at its peaks, indicating the need for adopting a sustainable control measures. It is worthy of note, that difficulty abounds in development and application of an effective diagnostic plan. It is therefore important to have effective immunogens which can be use in vaccination .

Cases of CLA in humans are rare and if reported in most cases it is related to exposure as a result of contact with infected animals. However, cases of CLA in humans due to the ingestion of raw cow and goat meat have been reported . In addition, about 25 cases of human infection have also been reported thus, indicating the zoonotic potential of CLA. Mills et al. (1997) reported a case of suppurative granulomatous lymphadenitis in a boy who has contact with farm animals. This finding validates the zoonotic implication of CLA and the need to develop an effective biosecurity measures to guard against infections to humans. Furthermore, Peel et al. (1997) in their review also reported that about 22 cases of human CLA is characterized by lymphadenitis, abscesses and other similar symptoms. In all cases, patients were treated with antibiotics and the affected lymph nodes surgically removed.

The clinical management of CLA revolves around early detection of the disease in a herd and culling of infected animals showing clinical manifestation of the disease. Due to the chronic nature of the disease, the tendency of the disease to spreading rapidly in the herd without the farmer knowing until the development of clinical manifestation is high . One of the major challenges in the management of CLA is attributed to the fact that many farmers and animal owners have little or no knowledge of the disease thus, facilitating the rapid spread of the disease among the herd. For instance, in Malaysia only about 14.8% of the farmers have knowledge of CLA . CLA disease causes significant economic loss to small ruminant industry, therefore, it is important to design measures that will aim at reducing the rate of spread of the disease.

For instance, bacteria induced caseation necrosis of the lymph nodes is one of the major manifestation of CLA in small ruminants and the organism have been known to persist within the infected lymph node. The most frequently observed clinical manifestation is abscess formation in the peripheral lymph nodes, subcutaneous tissue and involvement of the visceral organs . This is in agreement with the finding of this case report, because clinical history revealed a round firm swelling on the ventral side of the mandible and caseaous exudate upon excision (Figure 2). Furthermore, it has been observed that the abscess can persist for about two to three years containing the viable organism, thus, serving as a potential source of reinfection of the flocks .

Because CLA is a disease of great economic and zoonotic importance, there is the need to design an effective strategic plan for its control and eradication in areas where the disease is endemic. Such strategies can involve measures such as reducing the number of infected animals to such a level that it doesn’t pose a significant threat to animal welfare and public health. Other measures such as test and slaughter method should also be employed. The key to successful eradication of CLA in an endemic area involves the implementation of an active surveillance system supported by a fully equipped laboratory . Given the nature of the spread of CLA, the treatment of the disease is in effective and expensive. The best strategy adopted so far for the prevention and control of the disease in countries where the prevalence of the disease is high is through vaccination against the causative organism and this have however proven to give a very good result ; . An effective strategy however should be based on frequent clinical inspection, and serologic testing of all animals in the flock from time to time, including the recently purchased animals, and those that have been returned to the herd while culling those that are serologically positive or those showing clinical disease . This is because it has been observed that once the animal has been infected, it is difficult to completely eradicate the causative organism. For instance, in an eradication programme, there is need to accurately measure the predictive value of the test used in detecting the presence of CLA before a decision of culling an infected animal is made. This is because, increase or decrease in the prevalence of the disease affects the outcome of the test and thus can led to poor judgement which invariably results in under or over reporting the occurrence of the disease in a herd . In addition, given the important role played by subclinically infected animals in the introduction and spread of CLA into a herd, serological diagnosis has proven to be very useful in the control and eradication of CLA. Serological test such as compliment fixation test (CFT), ELISA, hemolysis inhibition test and immunodiffusion test are usually employed in the diagnosis of CLA. In spite of the limitations of these tests, ELISA has proven to be an exceptionally versatile tool in the control and eradication of CLA .

The implementation of biosecurity procedures in all flocks must especially during the introduction of new animals have showed reduction in the rate of infection . This is because; the focal point of entry of the disease into the herd is the introduction of new animals into the herd. In this case report it was observed that the farm have had a history of CLA even though the farm had been depopulate, the use of infective biosecurity measures might have been the cause of reinfection of the farm.

Other measures aimed at reducing the impact of the disease in order to reduce the associated losses due to the occurrence of the disease is involves effective control of insects and disinfecting the umbilical cord of the neonates and skin abrasions with 10% iodine . Measures aimed at reducing environmental risk such as the use of smooth wires to fence pens, proper and frequent disinfection of the ear tagging and shearing instruments should be encouraged . Furthermore, since majority of the farmers are not aware of the implication of the disease, it is important to help educate the animal owners and farm personnel on the economic importance of the disease and be encouraged to report any case of CLA to the veterinarians. In addition, information about the zoonotic potentials of the organism should be made available to farmers and people who live around the farm environment or are involved directly in taking care of the animals. Strict adherence to this control measures will greatly help in reducing the outbreak of CLA.

Conclusion

This clinical case showed the importance of effective implementation of vaccination strategies and other control measures in the control and prevention of CLA in small ruminants and its zoonotic implications in humans.

Acknowledgement

The authors wishes to appreciate the management and staff of University Veterinary Hospital, Universiti Putra Malaysia (UPM) for their cooperation.

Conflict of interest

None to declare.

Authors’ contribution

All authors contributed equally and approved the final manuscript.

References

  1. • Abdullah FFJ, Lau SS, Saharee AA, Shamsudin S (2011). Pathological changes in the organs of mice model inoculated with Corynebacterium pseudotuberculosis organism. Pertanika J. Trop. Agric. Sci. 34(1): 145-149.
  2. • Abdullah FFJ, Osman AY, Adamu L, Azri NA, Wahid A (2013). Caseous Lymphadenitis in a Goat. Vet. J. 52: 513-514.
  3. • Campbell SG, Ashfaq MK, Tashjian JJ, (1982) Caseous lymphadenitis in goats in the USA. In: Proceedings of the Third International Conference on Goat Production and Disease. Tucson, pp. 449-454.
  4. • Cetinkaya B, Karahan M, Atil E, Kalin R, De Baere T, Vaneechoutte M (2002). Identification of Corynebacterium pseudotuberculosis isolates from sheep and goats by PCR. Vet. Microbiol. 88(1): 75-83. http://dx.doi.org/10.1016/S0378-1135(02)00089-5[CrossRef]
  5. • de Sá Guimarães A, Do Carmo FB, Pauletti RB, Seyffert N, Ribeiro D, Lage AP, Gouveia AMG (2011). Caseous lymphadenitis: epidemiology, diagnosis, and control. IIOAB J. 2: 33-43.
  6. • Dercksen DP, Brinkhof JMA, Dekker-Nooren T, van Maanen K, Bode CF, Baird G, Kamp EM (2000). A comparison of four serological tests for the diagnosis of caseous lymphadenitis in sheep and goats. Vet. Microbiol. 75(2): 167-175. http://dx.doi.org/10.1016/S0378-1135(00)00217-0[CrossRef]
  7. • Dorella FA, Pacheco LGC, Oliveira SC, Miyoshi A, Azevedo V (2006). Corynebacterium pseudotuberculosis: microbiology, biochemical properties, pathogenesis and molecular studies of virulence. Vet. Res., 37(2): 201-218. http://dx.doi.org/10.1051/vetres:2005056[CrossRef]
  8. • Komala TS, Ramlan M, Yeoh NN, Surayani AR, Sharifah HSM (2008). A survey of caseous lymphadenitis in small ruminant farms from two districts in Perak, Malaysia-Kinta and Hilir Perak. Trop. Biomed. 25(3): 196-201.
  9. • Liu DT, Chan WM, Fan DS, Lam DS (2005). An infected hydrogel buckle with Corynebacterium pseudotuberculosis. Br. J. Ophthalmol. 89: 245–246. http://dx.doi.org/10.1136/bjo.2004.051698[CrossRef]
  10. • Mills AE, Mitchell RD, Lim EK (1997) Corynebacterium pseudotuberculosis is a cause of human necrotizing granulomatous lymphadenitis. Pathol. 29 (2): 231-233.
  11. • Møller K, Agerholm JS, Ahrens P, Jensen NE, Nielsen TK (2000). Abscess disease, caseous lymphadenitis, and pulmonary adenomatosis in imported sheep. J Vet. Med. Series B. 47(1): 55-62. http://dx.doi.org/10.1046/j.1439-0450.2000.00310.x[CrossRef]
  12. • Osman AY, Abdullah FFJB, Saharee AA (2012). Sero-Prevalence of Caseous Lymphadenitis Evaluated by Agar Gel Precipitation Test among Small Ruminant Flocks in East Coast Economic Regions in Peninsular Malaysia. J. Anim. Vet. Adv. 11: 3474-3480. http://dx.doi.org/10.3923/javaa.2012.3474.3480[CrossRef]
  13. • Osman AY, Abdullah FFJ, Chung ELT, Abba Y, Sadiq MA, Mohammed K, Lila MAM, Haron AW, Saharee AA (2015). Caseous Lymphadenitis in a Goat: A case report. Int. J. Livest. Res. 5: 128-132. http://dx.doi.org/10.5455/ijlr.20150221071744[CrossRef]
  14. • Paton MW, Rose IR, Hart RA, Sutherland SS, Mercy AR, Ellis TM, Dhaliwal JA (1994). New infection with Corynebacterium pseudotuberculosis reduces wool production. Aust. Vet. J. 71: 47-49. http://dx.doi.org/10.1111/j.1751-0813.1994.tb06152.x[CrossRef]
  15. • Peel MM, Palmer GG, Stacpoole AM, Kerr TG (1997). Human lymphadenitis due to Corynebacterium pseudotuberculosis: Report of ten cases from Australia and review. Clin. Infect. Dis. 24: 185–191. http://dx.doi.org/10.1093/clinids/24.2.185[CrossRef]
  16. • Roslindawani MN, Syafiqah AS, Jesse FFA, Effendy AW, Zamri-Saad M (2016). Recombinant caseous lymphadenitis vaccine with palm oil as adjuvant enhances the humoral and cell-mediated immune responses in rat model. J. Anim. Health Prod. 4: 22-25. http://dx.doi.org/10.14737/journal.jahp/2016/4.1.22.25[Full text][CrossRef]
  17. • Williamson LH (2001). Caseous lymphadenitis in small ruminants. Vet. Clinic. North Am. Food Anim. Pract. 17(2): 359-371. http://dx.doi.org/10.1016/S0749-0720(15)30033-5[CrossRef]
  18. • Windsor PA (2011). Control of caseous lymphadenitis. Vet. Clinic. North Am. Food Anim. Pract. 27(1): 193-202. http://dx.doi.org/10.1016/j.cvfa.2010.10.019[CrossRef]

Services

Article usage statistics

Loading…

Strategic Management of a Clinical Case of Recurrent Caseaous Lymphadenitis in a Goat Farm · ResearchersLinks