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Campylobacter Spp. in Whole Chickens and Viscera

Published: February 4, 2021
By: Bracho Espinoza, H. 1, Córdova, P.A. 2. / 1 National Experimental University Francisco de Miranda, Coro, Falcón, Venezuela; 2 Laboratory of Public Health, Faculty of Veterinary Sciences, Central University of Venezuela, Maracay, Aragua, Venezuela.
Summary

With the aim of detecting Campylobacter spp in benefited chickens and their viscera expended in the Girardot municipality, of the Aragua state, Venezuela, through a descriptive and retrospective investigation, a total of 48 chickens and their viscera were taken through a non-probability sample divided into three (03) lots, which were evaluated by means of a rapid plaque test, finding: Campylobacter spp. in lot (01) in 100% for chickens and viscera, in lot (02), 68.75% in chickens and 50% in viscera, and in lot (03) 75% in chickens and 56.5% in viscera; showing an overall positivity of 81.25% for whole chickens and 68.50% for viscera. The number of colony forming units (CFU), higher than the infecting dose for individual’s  ≥ 500 CFU, was obtained in 43.75% of the chickens and 25% of the viscera of the first lot; in 12.5% of chickens and entrails from the second lot, and in 6.25% in chickens and entrails from the third lot. In determining the degree of correlation between CFUs in chickens and viscera, an association (P <0.005) was observed between these variables.

Key Words: Campylobacter spp, packaged chickens, organ meats, Simplate® rapid plate test.

1. Introduction
The process of industrialization of the poultry sector has achieved a high degree of automation, however, such progress does not translate into an improvement in the quality of the meat, rather, they contribute to increase the microbial load of the poultry carcasses gaining importance today Campylobacter spp, among other microorganisms involved in food-(ETAs) transmitted diseases [1]. Infections among species of the family or Campylobacteraceae have campylobacteriosis Campylobacter enteritis, considered the most important in public health, its main agents are C. jejuni and C. coli (can also cause systemic infections and complications after infection; Agents Guillain Barre GBS) the impact of public health campylobacteriosis is increasing [2]. The genus Campylobacter, is dated and comprising gram negative bacilli curved (gullwing), with polar Flagellation,
Microaerophilic, do not use sugar, but energy of amino acids, are thermotolerant species 42 °C, zoonotic, birds are an important reservoir, are the causative agents of diarrhea in humans (first cause in industrialized countries and second or third cause in Latin America). They have been isolated 25 species and 9 subspecies [2]. Campylobacter spp, requires optimal growth conditions (5% O2, CO2 3-15% and 85% N), mentioned three species of thermophilic Campylobacter causing significant health problems in humans (C. jejuni, C. coli, and C. laridis) and outnumber cases of enteritis caused by Salmonella sp. and Shiguellas sp. [3]. According Seminar INFAL 2015 [4], following up on time pathogens Campylobacter spp, it was reported steadily increasing in England and Wales between 1997 and 2002 beating Rotavirus and Salmonella; even as [5]. At the Ninth International Congress of Tropical Medicine and Health held in Sweden indicated that cases of campylobacteriosis were more than doubled between 1988 and 2013, i.e. 3127 cases in 7499, an issue that has worsened since 1995. The center for Disease Control and Prevention (CDC) [6], in its surveillance program of Campylobacter spp, said that for this year experienced an increase of 14% over the years 2006-2008, noting that for every case of campylobacteriosis reported, there are 30 undiagnosed cases domestic and wild animals serve as host to the bacteria, causing pollution 90% of chicken carcasses during processing [7]. Studies conducted in Venezuela, specifically in the Aragua state by [8] reported Campylobacter spp in samples of whole, breasts, thighs and wings 75%, 95.83%, 83.33% and 70.83% respectively chickens, found in the first three samples indicated conditions≥500 units colony forming (CFU) per ml. Other researchers [9], [10] found Campylobacter spp in a 70.83% in liver and 48.95% in chicken gizzards; likewise [11] in Chile reported that poultry liver 95.1% recorded in Brazil isolation and a percentage that goes from 13.5 to 78.7. Campylobacteriosis is a zoonotic disease caused by eating food contaminated with bacteria of the genus Campylobacter: as raw milk, seafood, poultry and other animals (cross contamination), as well as in the untreated water; It occurs most often in children and young people, where it was reported 24.08 and 10.54% respectively in 2012 and in adults between 20 and 64 years and over reported 14.54 and 15.26. It is characterized by diarrhea, cramping, abdominal pain, fever, nausea and vomiting, some sequels neurological in which the syndrome Gillian Barre Syndrome (GBS) and Miller Fisher syndrome (MFS) [12]. The aim of the study was to analyze the prevalence of Campylobacter spp in whole chickens packed and viscera three lots traded in the municipality Girardot Aragua, Venezuela State through a quick test plate, and infer risk to which it is subjected consumer; also alert the population and institutions to exercise an active epidemiological surveillance in terms of ensuring public health. Campylobacteriosis were more than doubled between 1988 and 2013, i.e. 3127 cases in 7499, an issue that has worsened since 1995.
 
Conclusions
Detection of Campylobacter spp was 81.25% for chickens and 68.50% for the viscera, and found to lot 1 had the highest levels of contamination 100% for both samples, followed by lot 3, 75% and 68.75% respectively for broilers and viscera, and the lowest values were found detection in lot 2, with 68.75% chickens and 50% viscera, which is indicative of low hygienic conditions operability of chicken processing plants in the plots studied. Statistical results indicate a correlation between samples of chickens and viscera of the lots analyzed, indicative of the association between colony forming units, found in chickens, with those found in the viscera.  Based on the infective dose of bacteria to some individuals (≥500 CFU) in order to cause disease risk was represented by 43.75% chickens and 25% of the viscera of lot 1, and 12.5% for the samples studied in the lot 2 and finally 6.25% of the samples lot 3. It is observed that the hygienic conditions of the plants beneficiary chickens brands evaluated, lack of hygiene and control of critical points in the processing of products intended for human consumption.
 
This article was originally published in International Journal of Microbiology and Biotechnology. Vol. 2, No. 1, 2017, pp. 7-11. doi: 10.11648/j.ijmb.20170201.12. This is an Open Access article distributed under the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/).

[1] Molero, G.; Briceno, I. C.; Montiel, M.; Parra Y. C. 2012.Presence of Escherichia coli and mesophilic aerobic benefitchickens in Zulia state, Venezuela. XVI Venezuelan CongressProduction and Animal Industry. Rev. Scientific University of

Zulia. Vol. XXII (Supplement 1) 59.

[2] Fernandez, H. 2015. Methodological bases for bacteriological diagnosis of Campylobacter infections. In: Seminar Gender of Campylobacter, a group of bacteria Zoonotic of public health importance, Foodborne. Webinar INFAL / PAHO / WHO.

04/12/2015. Institute of Clinical Microbiology. Austral University of Chile. Valdivia.

[3] Odio, M. S. 1986. Evaluation of the microbiological quality of chicken meat in the metropolitan area of San Jose., Costa Rica. Work Degree in Microbiology. Costa Rica University. 45p.

[4] INFAL, 2015. Inter-American Network of Food Analysis Laboratories. Seminar: Gender Campylobacter, a group of bacteria Zoonotic of public health importance, Foodborne. Webinar INFAL / PAHO / WHO. 04/12/2015.

[5] Schmutz, C. 2015. Campylobacter surpassed Salmonella: analysis of Swiss surveillance data, 1988-2013. Trop. Med. Int. Health. Vol. 20 Suppl. 1.

[6] CDC. 2011. Department of Health and Human Services. In: Incidence and Trends of Foodborne Illness, USA. http://www.cdc.gov/food.net. Consultation in oct. 2015.

[7] Stern, N. J., Cray, F, Bailey, J. S., Cox, a., Craven, S. E., Hiett, k., Musgrove, M. T., Ladely, s., And Cosby D. Mead, G. C. 2001. Distribution of Campylobacter spp. in selected U: S, poultry production and processing operations. 64:11, 1705-1710.

[8] Veliz, N. 2006. Determination of Campylobacter spp. and aerobic mesophilic chicken samples benefited in the Municipality Girardot, Aragua, July-August 2004. Up Work Veterinary Science. Central University of Venezuela. 78p.

[9] Baublis, A. 1994. Prevalence of Campylobacter jejuni in two-slaughter chicken in Aragua state. Job promotion. University of Carabobo. 79p.

[10] Gomez, O. and Inojosa, Y. 2001. Prevalence of Campylobacter jejuni in chicken giblet meat obtained from outlets in Maracay Aragua state. Job promotion. University of Carabobo. 47p.

[11] CDC. 2010. Center of disease control. Campylobacter enteritis. In: http://wwwnc.cdc.gov/travel/yellowbook/2010/chapter-5/campylobacteenteritis.aspx  Consultation: July 2015.

[12] Bellido, A. Gonzalez, B., Galino, C., Smith, A., Tirado, M., Amedo, A., Safont, A. and Rameu, A. 2007. Risk factors for the occurrence of sporadic Campylobacter, Salmonella and rotavirus diarrhea in preschool children. An. Pediatric. 66, 367-374.

[13] Biocontrol Systems. 2000. Campylobacter indicator color. Bellevue, Washington, USACDC. 2010. Center of disease control. Campylobacter enteritis. In: http://wwwnc.cdc.gov/travel/yellowbook/2010/chapter-5/campylobacter enteritis.aspx.  Consultation: July 2015.

[14] Meldrum, R., Tuker, D. and Edwards, C. Baselines. 2004. Rates of Campylobacter and Salmonella in raw chicken in Wales, United Kingdom, in 2002. Journal Food Protection. 67, 1226-1228.

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Authors:
Héctor Bracho Espinoza
Universidad Nacional Experimental “Francisco de Miranda” (UNEFM)
Universidad Nacional Experimental “Francisco de Miranda” (UNEFM)
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