Skip to main content
Brazilian Journal of Microbiology logoLink to Brazilian Journal of Microbiology
. 2009 Sep 1;40(3):569–573. doi: 10.1590/S1517-838220090003000020

Occurrence of Salmonella spp. in broiler chicken carcasses and their susceptibility to antimicrobial agents

Dalila Angélica Moliterno Duarte 1,*, Aldemir Reginato Ribeiro 1, Ana Mércia Mendes Vasconcelos 1, Sylnei Barros Santos 1, Juliana Vital Domingos Silva 1, Patrícia Lúcia Arruda de Andrade 1, Lúcia Sadae Pereira da Costa de Arruda Falcão 1
PMCID: PMC3768528  PMID: 24031401

Abstract

The present study was carried out to evaluate the occurrence of Salmonellae in broiler chicken carcasses and to determine the antimicrobial resistance profile of the isolated strains. Twenty-five out of the 260 broiler chicken carcasses samples (9.6%) were positive for Salmonella. S. Enteritidis was the most frequent serovar. Nineteen Salmonella isolates were tested for antimicrobial resistance, and the results indicated that 94.7% were resistant to at least one antimicrobial agent. Resistance to streptomycin (73.7%), nitrofurantoin (52.3%), tetracycline (31.6%), and nalidixic acid (21%) were the prevalent amongst Salmonella strains tested.

Keywords: Salmonella, broiler chicken carcasses, antimicrobial resistance


The consumption of poultry meat has been increasing annually, bringing with it the concern about the cases of foodborne illness events caused by Salmonella (30), since poultry have been identified as a significant reservoir of Salmonella in the environment (29).

Regarding poultry health, there are three differents salmonellosis syndromes, two of them caused by no motile serovars and host-adapted to poultry, which are Pullorum Disease, caused by Salmonella Pullorum, and Fowl Typhoid, caused by Salmonella Gallinarum; the other syndrome is Paratyphoid Infections, caused by motile Salmonella serovars (29), which are also responsible for outbreaks of foodborne illness in humans.

The presence of Salmonella in the intestinal tract, on the skin and among the feathers of chickens, may cause carcasses contamination during slaughtering and processing (16) and is responsible by the introduction of Salmonella in the slaughterhouses, where will progress along the processing line, affecting the final microbiological quality and jeopardizing the consumers health(6).

The occurrence of Salmonella in chicken carcasses, in studies undertaken in different countries, can vary for instance from 13% in Poland (21) to 66% in Thailand (17). In Brazilian studies, they vary from 5.9% (20) to 42% (14).

In veterinary medicine, antimicrobial agents are used therapeutically, metaphylatically, prophylactically, and as growth promoters (28). However, their indiscriminate use is causing increasing resistance amongst Salmonella strains and other bacteria (7).

The present study was carried out to evaluate the occurrence of Salmonella spp. in broiler chicken carcasses and to estimate the resistance profiles of the isolates.

Two hundred and sixty broiler chicken carcasses were purchased in five processing plant located in Northeastern Brazil from April to December 2004. They were collected in sterilized plastic bags and transported, under refrigeration, to the Laboratory of Food Microbiology of the “Laboratório Nacional Agropecuário – Ministério da Agricultura, Pecuária e Abastecimento”, Recife, Pernambuco, Brazil.

Salmonella were isolated using the microbiological method recommended by the Brazilian Agriculture Ministry (“Ministério da Agricultura, Pecuária e Abastecimento”) (5). Complete antigenic characterization and serovar identification were performed by the Enteric Pathogens Laboratory from Oswaldo Cruz Institute Foundation, Rio de Janeiro (FIOCRUZ-RJ).

Nineteen Salmonella strains were tested for antimicrobial resistance by the disk diffusion method on Mueller-Hinton agar, according to the Clinical and Laboratory Standards Institute (CLSI, formely NCCLS)(11). The antimicrobials agents were: ampicillin 10 µg, amoxicillin/clavulonic acid, cefotaxime, ciprofloxacin 5 µg, chloranphenicol 30 µg, enrofloxacin 5 µg, gentamicin 10 µg, kanamycin 30 µg, nalidixic acid 30 µg, nitrofurantoin 300 µg, norfloxacin 10 µg, streptomycin 10 µg, polymyxin B 300 I.U., tetracycline 30 µg and trimethoprim/sulfamethoxazole. Escherichia coli ATCC 25922 was used as a reference strain. An isolate was classified as multiple resistant when demonstrated resistance to two or more agents (10).

Twenty-five out of the 260 broiler chicken carcasses samples (9.6%) were positive for Salmonellae. Others researches investigating the occurrence of Salmonella in different Brazilian States reported different levels in broiler chicken carcasses, 13% in Santa Catarina (19), 5.9% (20%), 32% (27), and 42% (14) in São Paulo, and 11.8% (23) in Ceará.

Surveys performed in different countries, using broiler chicken carcasses showed 13% in Poland ( 21), 29.3% in Belgian (31), 29.7% in UK (24), 35.8% in Spain (12), 62.5% in Senegal (3) and 66% in Thailand (17).

Twenty strains of Salmonella isolated in this study were identified at serovar level, from where it was identified 11 different Salmonella serovars. S. Enteritidis was the most frequent serovar (25%). The results obtained agree with the fact that S. Enteritidis was the predominant serovar associated with outbreaks in humans, as showed by the WHO Salmonella surveillance date for 1990-1995 (15), and with the fact that S. Enteritidis is the predominant in poultry carcasses and their products as showed in Belgium (31), in the United Kingdom (24), Spain (12) and Portugal (1).

In Brazil, S. Enteritidis has been the most prevalent serovar detected in human infections (13), in broiler chicken carcasses (27), in broiler chicken parts (26), and in poultry flocks (18).

The other isolates were S. Typhimurium (3 isolates), S. Saintpaul (3), S. Mbandaka (2), S. Corvallis (1), S. Heidelberg (1), S. Infantis (1), S. Munchen (1), S. Newport (1), S. Panama (1) and Salmonella. enterica subsp. enterica (O9,12) (1).

Antimicrobial resistance is a widely studied issue in all bacteria genera, mainly amongst zoonotic bacteria, like Salmonellae is.

Nineteen Salmonella isolates were tested for antimicrobial resistance, and the results (Table 1) indicated that 94.7% (n: 18) were resistant to at least one antimicrobial agent. This data is higher than the 58.1% observed in Greece (2), 67.3% in the United States (8), 75% in Portugal (1), but lower than the 100% obtained in Salmonellae isolated from broiler chicken carcasses by Cardoso et al. (9) in the State of Rio Grande do Sul, Brazil.

Table 1.

Antimicrobial resistence in Salmonella strain isolated from broiler chicken carcasses

Samples tested Number of strains tested Number of the resistance to antimicrobial agent
Amp. C Kan Enr Nor Tet Nal CTX Nit Est Gen Cip SXT Pol B AmC
S. Enteritidis 5 - - 1 - - 1 - - 5 3 - - - - -
S. Typhimurium 3 - - - - - - - - - 3 - - - - -
S. Saintpaul 2 - - - - - - 1 - 1 1 - - - - -
S. Mbandaka 2 1 1 1 - - 1 - - - 2 - - 1 - 1
S. Infantis 1 - - - - 1 1 1 - 1 1 - - - - -
S. Muenchen 1 - - - - - 1 - - - - - - - - -
S. Newport 1 - - 1 1 1 - 1 - - 1 - 1 - - -
S. Heidelberg 1 1 - 1 - - 1 - - 1 1 - - - - 1
S. Panama 1 - - - - - - 1 - - 1 - - - - -
S. Corvallis Salmonella 1 - - - - - - - - 1 1 - - - - -
enterica subsp. enterica (O9,12) 1 - - - - - 1 - - 1 1 - - - - -
Total 19 2 1 4 1 2 6 4 0 10 14 0 1 1 0 2

Resistance to streptomycin (73.7%), were higher than the 39% obtained by Antunes et al., (1) in Portugal, however lower than the 100% obtained by Ribeiro et al., (25) in S. Hadar isolated from broiler chicken carcasses in in the State of Rio Grande do Sul, Brazil.

The results regarding the resistance to nitrofurantoin (52.6%) and to tetracycline (31.6%) are supported by Oliveira et al. (22), who showed that 52.8% of S. Enteritidis strains isolated from bird carcasses, food, humans and poultry-related samples were resistant to nitrofurantoin. As well, it is supported by Antunes et al., (1), who found 36% resistance to tetracycline in Salmonella isolated from parts and broiler chicken carcasses in Portugal.

Resistance to the nalidixic acid (21%), norfloxacin (5.2%), enrofloxacin (5.2%) and ciprofloxacin (5.2%) were showed by some the Salmonella strains.

It was also observed resistence to Kanamycin (15.8%), ampicillin (10.5%), amoxicillin/clavulonic acid (10.5%), chloramphenicol (5.2%), trimethoprim/sulfamethoxazole (5.2%). None of Salmonella isolated showed resistance to cefotaxime, gentamicin and polimyxin B.

Fourteen different patterns of resistance were observed (table 3), two of them should be a concern because they showed resistance to eight different antimicrobial agents: CIP, ENR, KAN, NAL, NIT, NOR STR, TET, found in S. Newport and AMP, AMC, CHL, KAN, NIT, STR,SXT, TET, found in one S. Mbandaka.

Multiple resistance was not observed in 7 out of 19 tested strains, and 6 were resistant only to one antimicrobial agent, nalidixic acid (n: 1), nitrofurantoin (n: 2) and streptomycin (n: 3). One isolate identified as S. Muenchen, was susceptible to all antimicrobial agents.

Different factors may contribute to the Salmonella entry to the processing plants and to reach processed carcasses. Therefore any successful Salmonella control plan will need to implement actions to control contamination and dissemination of the bacteria in poultry raising sites (layers, hatcheries and chicken farms) (4), and in the slaughterhouses with a systematic laborers training, good manufacture practices and HACCP. Regarding the resistance to antimicrobial agents, the data obtained emphasize the need of a judiciously use of these agents in animal production, based on susceptibility tests.

Table 2.

Distribution of antimicrobial resistence patterns in Salmonella strains

Patterns Salmonella
Susceptible 1
Est. 3
Nal 1
Nit 2
Est, Nal 1
Est, Nit 3
Est, Tet 1
Nit, Tet 1
Est, Kan, Nit 1
Est, Nit, Tet 1
Amp, AmC, Est, Kan 1
Est, Nal, Nor, Tet 1
Amp, AmC, C, Est, Kan, Nit, SXT, Tet 1
Cip, Enr, Est, Kan, Nal, Nor, Nit, Tet 1

AMP: ampicilIN; AmC: amoxixilna + ácido clavulônico, CHL: chloramphenicol; CIP: ciprofloxacin;

ENR: enrofloxacin, STR: streptomycin; KAN: Kanamycin; NAL: nalidixic acid, NIT: nitrofurantoin;

NOR: norfloxacin, SXT: sulfametoxazol + trimetoprim, TET: tetracycline

Note: The opinions in this article are those of the authors and do not necessarily reflect views and policies of the organization to which they are affiliated.

RESUMO

Ocorrência de Salmonella spP. em carcaças de frango e sua suscetibilidade a agentes antimicrobianos

O presente estudo teve como objetivo verificar a ocorrência de Salmonellae em amostras de carcaças de frango e a suscetibilidade dos isolados a agentes antimicrobianos. Das 260 carcaças analisadas, 25 (9,6%) foram positivas para Salmonella. Salmonella Enteritidis foi o sorovar predominante. Com relação à suscetibilidade a agentes antimicrobianos, 94,7% das cepas de Salmonella testadas, apresentaram resistência a um ou mais agentes antimicrobianos. Os perfís de resistência mais comumente observados entre os isolados foram a resistência à estreptomicina (73,7%), nitrofurantoína (52,3%), tetraciclina (31,6%) e ácido nalidíxico (21%).

Palavras-Chave: Salmonella, carcaças de frango, resistência antimicrobiana

REFERENCES

  • 1.Antunes P., Réu C., Souza J.C., Peixe L., Pestana N. Incidence of Salmonella from poultry products and their susceptibility to antimicrobial agents. Int. J. Food Microbiol. 2003;82:97–103. doi: 10.1016/s0168-1605(02)00251-9. [DOI] [PubMed] [Google Scholar]
  • 2.Arvanitidou M., Tsakris A., Sofianou D., Katsouyannopoulos V. Antimicrobial resistance and R-factor transfer of salmonellae isolated from chicken carcasses in Greek hospitals. Int. J. Food Microbiol. 1998;40:197–201. doi: 10.1016/s0168-1605(98)00020-8. [DOI] [PubMed] [Google Scholar]
  • 3.Bada-Alambedji R., Fofana A., Seydi M., Akakpo A.J. Antimicrobial Resistance of Salmonella isolated from poultry carcasses in Dakar (Senegal). Braz. J. Microbiol. 2006;37:510–515. [Google Scholar]
  • 4.Bailey J.S., Stern N.J., Fedorka-Cray P., Craven S.E., Cox N.A., Cosby D.E., Ladely S., Musgrove M.T. Sources and movement of Salmonella through integrated poultry operations: a multistate epidemiolgical investigation. J. Food Prot. 2001;64:1690–1697. doi: 10.4315/0362-028x-64.11.1690. [DOI] [PubMed] [Google Scholar]
  • 5.Brasil. Brasília: Instrução Normativa 62, de 26 de agosto de 2003.; 2003. Ministério da Agricultura, Pecuária e Abastecimento. Métodos analíticos oficiais para análises microbiológicas para o controle de produtos de origem animal e água. Diário Oficial [da] Republica Federativa do Brasil. pp. 14–50. 18 setembro de 2003. Seção I. [Google Scholar]
  • 6.Berchieri Júnior A., Paulilo A.C., Fernandes S.A., Pessoa G.V.A., Rossi Junior O.D., Irino K., Ávila F.A., Calzada C.T. Salmonella em um abatedouro avícola. Ars Vet. 1987;3:81–87. [Google Scholar]
  • 7.Berchieri Júnior A., Adachi S.Y., Calzada C.T., Paulillo A.C., Schoken-Iturrino R.P., Tavechio A.T. Farinha de carne como fonte de Salmonella em granja avícola. Pes. Vet. Bras. 1989;9:9–12. [Google Scholar]
  • 8.Bokanyi Júnior R.P., Stephens J.F., Foster D.N. Isolation and characterization of Salmonella from croiler carcasses or parts. Poul. Sci. 1990;69:592–598. doi: 10.3382/ps.0690592. [DOI] [PubMed] [Google Scholar]
  • 9.Cardoso M.O., Ribeiro A.R., Santos L.R., Pilotto F., Moraes H.L.S., Salle C.T.P., Roscha S.L.S., Nascimento V.P. Antibiotic resistance in Salmonella Enteritidis isolated from broiler carcasses. Braz. J. Microbiol. 2006;37:299–302. [Google Scholar]
  • 10.Carramiñana J.J., Rota C., Agústin I., Herrera A. High prevalence of multiple resistance to antibiotics in Salmonella serovars isolated from a poultry slaugterhouse in Spain. Vet. Microbiol. 2004;104:133–139. doi: 10.1016/j.vetmic.2004.08.010. [DOI] [PubMed] [Google Scholar]
  • 11.Clinical and Laboratory Standards Institute (CLSI, formerly NCCLS – National Committee for Clinical Laboratory Standards). USA: Document M2-A8. Wayne, Pennsylvani; 2003. Performance Standards for Antimicrobial Disk Susceptibility tests; Approved Standard – Eightth NCCLS. [Google Scholar]
  • 12.Dominguez C., Gómez I., Zumalacárregui J. Prevalence of Salmonella and Campylobacter in retail chicken meat in Spain. Int. J. Food Microbiol. 2002;72:165–168. doi: 10.1016/s0168-1605(01)00638-9. [DOI] [PubMed] [Google Scholar]
  • 13.Fernandes S.A., Tavechio A.T., Ghilardi A.C.R., Dias A.M.G., Almeida I.A.Z.C., Melo L.C.V. Salmonella serovars isolated from humanin São Paulo State, Brazil, 1996-2003. Rev. Inst. Med. Trop. S. Paulo. 2006;48:179–184. doi: 10.1590/s0036-46652006000400001. [DOI] [PubMed] [Google Scholar]
  • 14.Fuzihara T.O., Fernandes S.A., Franco B.D.G.M. Prevalence and dissemination of Salmonella serotypes along the slaughtering process in Brazilian small poultry slaughterhouses. J. Food Prot. 2000;63:1749–1753. doi: 10.4315/0362-028x-63.12.1749. [DOI] [PubMed] [Google Scholar]
  • 15.Herikstad H., Motarjemi Y., Tauxe R.V. Salmonella surveillance: a global of public healh serotyping. Epidem. Infec. 2002;129:1–8. doi: 10.1017/s0950268802006842. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 16.Humphrey T.J., Mead G.C., Rowe B. Poultry meat as a source of human salmonellosis in England and Wales. Epidem. Infec. 1988;100:175–184. doi: 10.1017/s0950268800067303. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 17.Jergklinchan J., Koowatananukul C., Daengprom K., Saitanu K. Occurrence of Salmonellae in raw broiler and their products in Thailand. J. Food Prot. 1994;57:808–810. doi: 10.4315/0362-028X-57.9.808. [DOI] [PubMed] [Google Scholar]
  • 18.Kanashiro A.M., Stoppa G.F.Z., Cardoso A.L.S.P., Tessari E.N.C., Castro A.G.M. Serovars of Salmonella spp. isolated from broiler chickens and commercial breeders in diverse regions in Brazil July 1997 to December 2004. Braz. J. Poultry. Sci. 2005;7:195–198. [Google Scholar]
  • 19.Machado R.A., Tosin I., Leitão M.F.F. Occurrence of Salmonella sp. and Campylobacter sp. in chickens during industrial processing. Rev. Microbiol. 1994;25:239–244. [Google Scholar]
  • 20.Matheus D.P., Rudge A.C., Gomes S.M.M. Ocorrência de Salmonella spp. em carne de frango comercializada no município de Bauru, SP, Brasil. Rev. Inst. Adolfo Lutz. 2003;62:111–115. [Google Scholar]
  • 21.Mikolajczyk A., Radkowski M. Salmonella spp. on chicken carcasses in processing plants in Poland. J. Food Prot. 2002;65:1475–1479. doi: 10.4315/0362-028x-65.9.1475. [DOI] [PubMed] [Google Scholar]
  • 22.Oliveira S.D., Flores S.F., Santos L.R., Brandelli A. Antimicrobial resistance in Salmonella enteritidis strains isolated from broiler carcasses, food, human and poultry-related samples. Int. J. Food Microbiol. 2005;97:297–305. doi: 10.1016/j.ijfoodmicro.2004.04.022. [DOI] [PubMed] [Google Scholar]
  • 23.Oliveira W.F., Cardoso W.M., Salles R.P.R., Romão J.M., Teixeira R.S.C., Câmara S.R., Siqueira A.A., Marques L.C.L. Initial identification and sensitivity to anitmicrobial agents of Salmonella sp. isolated from poultry products in the State of Ceará, Brazil. Braz. J. Poultry. Sci. 2006;8:193–199. [Google Scholar]
  • 24.Plummer R.A.S., Blissett S.J., Dodd C.R. Salmonella contamination of retails chicken products sold in the UK. J. Food Prot. 1995;58:843–846. doi: 10.4315/0362-028X-58.8.843. [DOI] [PubMed] [Google Scholar]
  • 25.Ribeiro A.R., Kellermann A., Santos L.R., Fittél A.P., Nascimento V.P. Resistência antimicrobiana em Salmonella enterica subsp. enterica Sorovar Hadar isoladas de carcaças de frango. Arq. Inst. Biol. 2006;73:357–360. [Google Scholar]
  • 26.Ribeiro A.R., Kellermann A., Santos L.R., Bessa M.J., Nascimento V.P. Salmonella spp. In raw broiler parts: occurrance, antimicrobial resistance profile and phage typing of the Salmonella Enteritidis isolates. Braz. J. Microbiol. 2007;38:296–299. [Google Scholar]
  • 27.Santos S.M.S., Berchieri Jr. A., Fernandes S.A., Tavechio A.T., Amaral L.A. Salmonella em carcaças de frango congeladas. Pes. Vet. Bras. 2000;20:39–42. [Google Scholar]
  • 28.Schwarz S., Kehrenberg C., Walsh T.R. Use of antimicrobial agents in veterinary medicine and food animal production. Int. J. Antimicrob. Agents. 2001;17:431–437. doi: 10.1016/s0924-8579(01)00297-7. [DOI] [PubMed] [Google Scholar]
  • 29.Snoeyenbos G.H., Williams J.E. Salmonellosis. In: Calnek B.W., editor. Diseases of Poultry. 9th. Ed. Iowa: Iowa State University Press. Ames; 1991. pp. 72–73. [Google Scholar]
  • 30.Todd E.C.D. Poultry-associated foodborne disease - its occurrence, cost, sources and prevention. J. Food Prot. 1980;43:129–139. doi: 10.4315/0362-028X-43.2.129. [DOI] [PubMed] [Google Scholar]
  • 31.Uyttendaele M.R., Debevere J.M., Lips R.M., Neyts K.D. Prevalence of Salmonella in poultry carcasses and their products in Belgium. Int. J. Food Microbiol. 1998;40:1–8. doi: 10.1016/s0168-1605(98)00012-9. [DOI] [PubMed] [Google Scholar]

Articles from Brazilian Journal of Microbiology are provided here courtesy of Brazilian Society of Microbiology

RESOURCES