Comparative Study on the Efficacy of Some Antimycoplasma Drugs on the Performance of Commercial Broiler Flocks from Infected Breeders

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Global Veterinaria 3 (2): 69-74, 2009 ISSN 1992-6197 IDOSI Publications, 2009 Comparative Study on the Efficacy of Some Antimycoplasma Drugs on the Performance of Commercial Broiler Flocks from Infected Breeders 1 2 3 4 M.M. Amer, A. El-H.A. Hanafei, K.M. El-Bayomi and G.A. Zohair 1 Department of Poultry Diseases, Faculty of Veterinary Medicine, Cairo University, Giza, Egypt 2 El-Wadi Poultry Company, Giza, Egypt 3 Department of Poultry Diseases, National Research Center, Dokki, Giza, Egypt 4 Department of Animal Production, Faculty of Agriculture, Sanaa University, Yemen Abstract: In this field 3 trials, 60 000 Ross broiler chicks were used. Air sac lesion, cumulative mortality, average body weight gain, feed consumption, feed conversion rate and European efficacy factor were used to evaluate the efficacy of some antimycoplasma drugs on the performance of commercial broiler flocks derived from Mycoplasma infected breeders. Lincospectin, Pulmotil and Tylan were administered in drinking water at 1 day old and repeated at 19 days. Mycoplasma infection in the used chicks was confirmed by clinical signs, air sac lesions, positive results to serum agglutination test for Mycoplasma gallisepticum (MG) and Mycoplasma synoviae (MS). MG antigen was detected in tracheal sections by immuno-histochemistry. The obtained results proved that the used antimycoplasma drugs still effective in controlling of Mycoplasmosis in broilers and their efficiency varied by repeated successive use in flocks reared in the same house. Pulmotil showed stable results, followed by Lincospectin and tylan. It was concluded that antimycoplasma drug administration in broiler from infected breeders have a marked role in improvement of their performance. Key words: Mycoplasmosis Antimycoplasma drugs Broiler chickens Lincospectin Pulmotil Tylan Performance INTRODUCTION Both MG and MS were reported as a wide spread chicken pathogens among Egyptian chicken flocks by Both Mycoplasma gallisepticum (MG) and either serologically and /or isolation and identification Mycoplasma synoviae (MS) are frequently incriminated methods [6-11]. to cause infectious chronic respiratory disease (CRD) Antimycoplasma drugs are used intensively to in chickens characterized by respiratory signs, decreased improve productivity and reproductivity of layers growth and hatchability rates, decreased egg production, [12, 13] as well as broiler [4] flocks. The massive use of and downgrading of carcasses at slaughter due to such drugs resulted in development of antimycoplasma airsacculitis and arthritis [1]. In the same time, the resistant Ms and MG strains [14-17]. increased medication costs are additional factors The current field studies in 3 trials; 4 flocks each; which considered as source of economic losses that had been carried out to compare effect of 3 wide used make this disease as one of the costliest problems antimycoplasma drugs including Lincospectin, Pulmotil confronting commercial poultry production [2]. and Tylan on performance of commercial broiler Ross Prevention and control programs of Mycoplasmosis breed flocks derived from infected breeders and show include surveillance (serology, culture, isolation and clinical signs, serological and immuno-histochemistry identification) and vaccination, account for additional positive results. costs [3, 4]. A complete review of the approximate 25 year history of MG immunization in USA indicated that MATERIALS AND METHODS the economic loss due to downgrading, reduced feed efficiency, and medication costs make MG infection Chicken Flocks: This field study was carried out on one of the costliest diseases confronting the poultry 60 000 commercial broiler Ross breed chicks in 3 industry [5]. replicates. Each replicate 20 000 chicks in 4 closed houses Corresponding Author: Dr. M.M. Amer, Department of Poultry Diseases, Faculty of Veterinary Medicine, Cairo University, Giza, Egypt 69

Table 1: Drugs used doses, age of administration and concentration in Table 2: Results of SPA test on sera of 1 day old chicks against MG and drinking water MS colored antigens (n= 25 samples/trial) Dose at 1 day old Dose at 19 days Conc. in D.W Drug (mg/bird) (mg/k.gm) (/200 L) Lincospectin 0.1 0.2 150.0 gm Pulmotil 2.0 15.0 60.0 ml Tylan 35.0 70.0 100.0 gm D.W: Drinking water (5000 chicks/house). The chicks were obtained from breeder flock infected with Mycoplasma. All trials were done in successively same houses. Chicks were reared under similar management and environmental conditions. Ration: The chicks were feed on prepared ration according to Ross broiler management manual and National Research Council [18] requirement for broiler. All housed chickens were given ration adlibitum. Diagnosis of Mycoplasmosis: The used 1- day- old chicks were sampled (blood for serum 25 samples/ trial in addition to specimens from lungs and tracheae) and tested using the following methods: 1. Serum Plate agglutination (SPA) test. SPA-test was carried out using 0.02 ml of serum, mixed with 0.02 ml of stained antigen of MG or MS, clumping within 2-3 minute indicates positive result [1, 19]. Stained M.G and MS antigens for SPA test were obtained from "Intervet International BV Boximeer-Holland" (Table 2). 2. Immuno-histochemistry: It was carried out using peroxidase detection kit purchased from Novocastra Co. lot No. 711010 on sections of tracheae and lungs from chicks with suspected signs and lesions [20]. Results are shown in Fig. 2. 3. Air Sac Lesions: The air sacs of dead chickens and in slaughter house were examined [21]. MG MS Trial -------------------------------- ---------------------------------- number No. of positive % No. of positive % 1 2 8 0 0 2 4 16 2 8 3 7 28 3 12 SPA: Serum Plate agglutination, MG: Mycoplasma gallisepticum, MS: Mycoplasma synoviae. Drugs and Medication: The following commercial antimycoplasma products including combination of Lincomycin and Spectinomycin (Lincospectin ), Tilmilcosin (Pulmotil AC ) and Tylosin tarterate (Tylan ) were used. Each product was repeatedly used for chicks reared in the same house. Doses, age of administration and concentration in drinking water are shown in Table 1. Broiler performance parameters: Broiler performance parameters including average cumulative mortality rate (CMR), body weight/g, cumulative feed intake/g (CFI/g), cumulative feed conversion rate (CFCR) and European efficacy factor (EEF) were used and calculated as shown in Table 3 Fig. 3-6 [22]. Good efficiency is considered to have an EEF > 280, while low efficiency has an EEF < 220. RESULTS Some chicks showed signs of ruffling; gasping of air, st closed eye and difficult breathing from the 1 day of life (Fig. 1A) and post-mortem examination of scarified chicks reveals yellow casious material in air sacs (Fig. 1B). The tested tracheal sections with Immuno-histochemistry showed MG antigen in stained tracheae of such chicks (Fig. 2B). Fig. 1: One-day -old chick from mycoplasma positive Ross broiler breeders showing: A) Gasping of air, closed eye and difficult breathing; B) Yellow casious material in abdominal air sacs. 70

Fig. 2: Immuno-peroxidase stained tracheal sections with haematoxylin as counter stain showing: A) Specific brown staining of M G antigen at the apical border of the lining epithelial cells (40 X) B) Negative tracheal tissue (40 X) Table 3: Effect of antimycoplasma drugs on productivity of seropositive broiler chicks Trial No. House No. Treatment Age/Days CMR* Body weight/gm CFI/gm** CFCR *** EEF**** 1 1 Lincospectin 35 1.44 2008 3218 1.60 351 2 Pulmotil 1.12 1998 3191 1.60 350 3 Tylan 1.12 1985 3184 1.60 347 4 Control 1.51 1907 3131 1.64 325 2 1 Lincospectin 33 2.80 1735 2883 1.66 304 2 Pulmotil 3.60 1809 2989 1.65 314 3 Tylan 3.00 1806 2937 1.63 321 4 Control 3.30 1639 2716 1.66 284 3 1 Lincospectin 34 4.40 1770 2891 1.63 299 2 Pulmotil 3.00 1819 2794 1.53 339 3 Tylan 4.70 1719 2893 1.68 282 4 Control 3.30 1708 2815 1.65 290 * CMR: Cumulative Mortality Rate, ** CFI/gm.: Cumulative Feed intake/grams, *** CFCR: Cumulative Feed Conversion Rate, **** EEF: European Efficacy Factor. The tested diluted sera of 1 day old chicks showed Pulmotil groups are the highest in trial 2 and 3 as positive results to SPA -test against stained antigen of compared with tylan. Lincospectin showed variable MG in 2/25 (8%), 4/25 (16%) and 7/25 (28%) and for MS in results. 0/25 (0%), 2/25 (8%) and 3/25 (12%) in trial 1, 2 and 3; CFI/gm in control houses was lower than those of respectively (Table 2). medicated ones in all trials. Pulmotil in trial 1and 3 showed Air sac lesions in dead and during processing lower feed intake as compared with other treatments. were varied from apparent normal to slight turbidity CFCR of non medicated house was generally lower without marked difference between medicated groups. than medicated (Table 3) in all trials, except that of tylan Non medicated controls showed thickened air sac wall in trial 3 that is lowest, as compared with medicated and sometimes with fibrinous exudates. non medicated in all trials. The highest CFCR was that of CMR in medicated houses are lower than that tylan in trial 2 and Pulmotil in trial 3. of their non medicated control (Table 3, Fig. 3). EEF of treated and non medicated houses > 280 can Pulmotil medicated house showed the lowest CMR, be evaluated as good. Medicated houses in trials 1 and 2 while Lincospectin and tylan groups are higher. were higher than non medicated (Fig. 6). Average body weights/g (Fig. 4) in medicated Pulmotil was the most effective and gives relatively houses is higher than their non medicated controls. stable results followed by Lincospectin and tylan. 71

The used chicken flocks in this study were proved to be infected with mycoplasma according to the recorded signs (Fig. 1A), air sac lesions (Fig. 1B) and results of SPA as well as Immuno- histochemistry (Fig. 2) that agree with [4]. The recorded gross lesions in dead and during processing as the prevalence of air sac lesions were varied from apparent normal to slight turbidity without Fig. 3: Effect of antimycoplasma drugs on cumulative marked difference between medicated groups, while non mortality rate (CMR) of seropositive broiler chicks medicated control showed thickened air sac wall with fibrinous exudates. The result indicated that the used drugs played a role in controlling infection [4, 23] and limitation of gross lesions [15, 23-25]. Also the 3 used drugs still effective [26, 27]. Cumulative mortality rate (CMR) in medicated houses trials 1 (1.44, 1.12, and 1.12) and trials 2 (2.80, 3.60 and 3.00) are lower than those of their non medicated controls (1.51, 3.30 and 3.30); respectively. The results indicated that administration of lincospectin, Pulmotil and tylan have value in reducing mortalities in mycoplasma infected Fig. 4: Effect of antimycoplasma drugs on body chickens [28]. weight/gm of seropositive broiler chicks CMR recorded in trial 3 showing that value of Pulmotil medicated house (3.0) is the lowest, while Lincospectin (4.40) and tylan (4.70) groups are higher than Pulmotil (3.00) and non medicated control (3.30). This result indicated that repeated use of Pulmotil still effective, while efficacy of lincospectin and tylan in the ed 3 repeated use in the same house started to be lower. This observation is agreed with literature [15, 28]. Average body weights/g (Table 3, Fig. 4) in medicated houses of trial 1 (2008, 1998, and 1985) and trial 2 (1735, 1809 and 1806) and trial 3 (1770, 1819 and 1719) are higher than non medicated control houses; Fig. 5: Effect of antimycoplasma drugs on cumulative 1907, 1639 and 1708; respectively. Values in Pulmotil feed intake (CFI)/gm of seropositive broiler chicks treated groups are the highest [29, 30] in trial 2 and 3 as compared with the lowest value in tylan houses [31], while results of lincospectin are variable. Comparing cumulative feed intake/g (CFI/g.) in control houses was lower than those of medicated ones in all trials. Pulmotil in trials 1and 3 showed lower feed intake as compared with the other two drugs. Cumulative feed conversion rate (CFCR) of Lincospectin and Pulmotil medicated houses were lower than non medicated in all trials. Tylan medicated house in trial 3 that showed the lowest CFCR (1.68) as compared with medicated and non medicated houses in all trials. The Fig. 6: Effect of antimycoplasma drugs on European highest CFCR was that of Pulmotil (1.53) in trial 3. Efficacy Factor (EEF) of seropositive broiler Generally; the calculated European Efficacy Factor chicks (EEF) of treated and non medicated houses > 280 (Table 72 DISCUSSION

3, Fig. 6) can be evaluated as good. The medicated houses 9. Shaker, M.M., 1995. Microbiological studies on in trial 1 and 2 are higher than non medicated, Lincospectin (351), tylan (321) and Pulmotil (339) in trial 1, 2 and 3; respectively. It was clear that the average mortality and feed intake were higher with lower body weights and conversions in non medicated than medicated [32]. These results supported the use of such drugs in improvement of infected broilers and in agreement with available data [4, 28, 31]. In conclusion, the used antimycoplasma drugs still effective in controlling of Mycoplasmosis in broilers derived from infected breeders, and the efficiency varied by repeated use in successive flocks. Pulmotil was the most effective and stabled one followed by Lincospectin and tylan. REFERENCES 1. Kleven, S.H., 1998. Mycoplasmas in the etiology of multifactorial respiratory disease. Poultry Science, 77: 1146-1149. 2. Ley, D.H. and A.P. Avakian, 1992. An outbreak of Mycoplasma synoviae infection in North Carolina turkeys: Comparison of isolates by sodium dodecyl sulfate-polyacrylamide gel electrophoresis and restriction endonuclease analysis. Avian Disease, 36: 672-678. 3. Mohammed, H.O., T.E. Carpenter and R. Yamamoto, 1987. Economic impact of Mycoplasma gallisepticum and Mycoplasma synoviae in commercial layer flocks. Avian Disease, 31: 477-482. 4. Saif, Y.M., H.J. Barnes, A.M. Fadly, J.R. Glisson and D. E. Swayne, 2003. Poultry Diseases, 11 th Edition., Iowa State Press, Iowa, pp: 719-774. 5. Yoder, H.W., 1978. Mycoplasma gallisepticum th infections. In: Diseases of Poultry. 7 Edition., M.S. Hosted, B.W. Calnek, C.F. Helmboldt, W.M. Reid, and H.W. Yoder, Jr., Iowa State Univ. Press, Ames, Iowa, pp: 236-250. 6. El-Shater, S.A.A., A.M.W. Khair El Din and F. Oraby, 1990. Incidence of mycoplasma in gallinaceous th birds. 4 Science. Congress, Faculty of Veterinary Medicine, Assiut University, pp: 1003-1010. 7. Soliman, A.M., 1990. Status of Mycoplasma synoviae in chicken in Upper Egypt. Assiut Veterinary Medicine Journal, 23: 00-00. 8. Dardeer, M.A.A., 1992. Some studies on mycoplasma in poultry. Master in Veterinary Science (Thesis). Department of animal Medicine, Faculty of Veterinary Medicine, Cairo University. 73 mycoplasma infection in poultry. Ph.D. (Thesis), Microbiology Department, Faculty of Veterinary Medicine, Cairo University. 10. Saif-Edin, M., 1997. Situation of mycoplasma infections among chickens in upper Egypt with evaluation of different diagnostic techniques. Assiut. Veterinary Medicine Journal, 37: 54-67. 11. Abou El Makarem, M. M., 2003. Evaluation of serological tests for the diagnosis of M. gallisepticum in comparison with the frequency of isolation. Assiut Veterinary Medicine Journal, 49: 220-227. 12. Carpenter, T.E., E.T. Mallinson, K.F. Miller, R.F. Gentry and L.D. Schwartz, 1981. Vaccination with F-Strain Mycoplasma gallisepticum to reduce production losses in layer chickens. Avian Disease, 25: 404-409. 13. Levisohn, S. and S.H. Kleven, 2000. Avian mycoplasmosis (Mycoplasma gallisepticum). Rev Scientific Technology, 19: 425-442. 14. Tanner, A.C. and Wu, Ching-Ching, 1992. Adaptation of the sensititre broth Microdilution technique to antimicrobial susceptibility testing of Mycoplasma gallisepticum. Avian Disease, 36: 714-717. 15. Jordan, F.T.W. and B.K. Horrocks, 1996. The minimum inhibitory concentration of tilmicosin and tylosin for Mycoplasma gallisepticum and Mycoplasma synoviae and a comparison of their efficacy in the control of Mycoplasma gallisepticum infection in broiler chicks. Avian Disease, 40: 326-334. 16. Gautier-Bouchardon, A.V., A.K. Reinhardt, M. Kobisc, and I. Kempf, 2000. In vitro development of resistance to enrofloxacin, erythromycin, tylosin, tiamulin and oxytetracycline in Mycoplasma gallisepticum, Mycoplasma iowa and Mycoplasma synoviae. Veterinary Microbiology, 88: 47-58. 17. Stipkovits, L.T., 2000. Current questions of the control of Mycoplasma synoviae infection. Magyar Allatorvosok Lapja, 122: 165-167. 18. Ewing, M.L., L.H. Lauerman, S.H. Kleven and B. Brown, 1996. Evaluation of diagnostic procedures to detect Mycoplasma synoviae in commercial multiplier-breeder farms and commercial hatcheries in Florida. Avian Disease, 40: 798-806. 19. National Research Council (NRC), 1984. National requirement for poultry. 9 Ed., Washington DC, th National Academy Press.

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