Poultry Feces Research Articles

Whole genome sequencing of multidrug-resistant Salmonella enterica serovar Typhimurium isolated from humans and poultry in Burkina Faso

BackgroundMultidrug-resistant Salmonella is an important cause of morbidity and mortality in developing countries. The aim of this study was to characterize and compare multidrug-resistant Salmonella enterica serovar Typhimurium isolates from patients and poultry feces.MethodsSalmonella strains were isolated from poultry and patients using standard bacteriological methods described in previous studies. The strains were serotype according to Kaufmann-White scheme and tested for antibiotic susceptibility to 12 different antimicrobial agents using the disk diffusion method. The whole genome of the S. Typhimurium isolates was analyzed using Illumina technology and compared with 20 isolates of S. Typhimurium for which the ST has been deposited in a global MLST database.The ResFinder Web server was used to find the antibiotic resistance genes from whole genome sequencing (WGS) data. For comparative genomics, publicly available complete and draft genomes of different S. Typhimurium laboratory-adapted strains were downloaded from GenBank.ResultsAll the tested Salmonella serotype Typhimurium were multiresistant to five commonly used antibiotics (ampicillin, chloramphenicol, streptomycin, sulfonamide, and trimethoprim). The multilocus sequence type ST313 was detected from all the strains. Our sequences were very similar to S. Typhimurium ST313 strain D23580 isolated from a patient with invasive non-typhoid Salmonella (NTS) infection in Malawi, also located in sub-Saharan Africa. The use of ResFinder web server on the whole genome of the strains showed a resistance to aminoglycoside associated with carriage of the following resistances genes: strA, strB, and aadA1; resistance to β-lactams associated with carriage of a blaTEM-1B genes; resistance to phenicol associated with carriage of catA1 gene; resistance to sulfonamide associated with carriage of sul1 and sul2 genes; resistance to tetracycline associated with carriage of tet B gene; and resistance to trimethoprim associated to dfrA1 gene for all the isolates.ConclusionThe poultry and human isolates were genetically similar showing a potential food safety risk for consumers. Our finding of multidrug-resistant S. Typhimurium ST313 in poultry feces calls for further studies to clarify the potential reservoirs of this emerging pathogen.

Biogas Production from Poultry Faeces

Poultry faeces management is multidimensional, which involves in public health, waste management, utilization of fertilizing value and energy production issues. The paper attempts to depict the poultry faeces management by bioconversion technology. Biogas may be the tool of energy generation in rural/remote areas while appropriate technique of waste management in urban centers of developing countries. Biogas production from poultry faeces can prevent soil, ground water contamination, crop diseases, and public health resulting ameliorate environment. Three cycles of varying dose are conceded for searching optimum generation of biogas with modified Gobar Gas Company (GGC) 2047 model. The result has displayed as cumulative volume of produced gas.

Viral metagenomics analysis of poultry faeces in live poultry market, Haikou, China

Objective: To conduct in-depth study of the distribution and diversity of viruses in poultry is of great importance in monitoring the emergence of interspecies transmission of novel viruses that may cause epidemics with public health significance. Poultry is an economically important source of meat, eggs and feathers which plays an important role as natural reservoirs of many pathogenic viruses. Compared with wild animals, poultry have more frequent interactions and therefore opportunities to transmit their viruses to human. Methods: To study the viromes of different types of poultry in Hainan, China, we used metagenomics for deep viral nucleic acid sequencing of the faecal samples collected from chickens, ducks and pigeons from a live poultry market in Haikou. Result: The poultry viromes were identified by sequence similarity comparisons of viral reads (BLASTxE score, <5) against viral reference database. A total of 15 309 viral reads were obtained, approximately 13 063, 1 370 and 876 viral reads were generated from the chicken, duck, pigeon faecal samples, respectively. The majority of the sequences were homologous to the animal virus of Adenoviridae, Herpeaviridae, Picobirnaviridae, Reoviridae, Retroviridae, Circoviridae, Paramyxoviridae, Astroviridae, Caliciviridae, Coronaviridae, Picornaviridae, and Orthomyxoviridae. The VP4 and VP7 segments of a pigeon rotavirus, similar to fox rotavirus in group A, were sequenced and phylogenetically analyzed. The near full genome of a pigeon circovirus was also analyzed. Conclusion: The major types of poultry in a Haikou harbor many different families of viruses in their feces which may have the potential for interspecies transmissions. Further studies should be conducted to identify the most prevalent and important viruses among a larger number of poultry in Haikou and other areas in Hainan.

Characterization of Campylobacter jejuni samples coming form poultry meat and feces

Background Campylobacter jejuni is one of the main causal agents of food borne diseases. Infections with this pathogen are mainly caused by chicken meat consumption. Aim To characterize antibiotic resistance and virulence factors in C. jejuni strains obtained from chicken meat and poultry feces in Central Chile. Material and Methods The presence of C. jejuni in 30 meat and 40 feces samples from poultry was studied. From these samples, we obtained 40 strains which were characterized at the molecular level for the presence of 16 genes involved in virulence using PCR. In parallel, antibiotic resistance for ciprofloxacin, nalidixic acid, tetracycline, erythromycin, azithromycin, chloramphenicol y ampicillin was analyzed. Results Twenty and 63% of feces and chicken meat samples were positive for C. jejuni, respectively. Moreover, a high percentage of strains showed antibiotic resistance, where 27% of strains were resistant to all tested antibiotics, except for azithromycin. Finally, 10% of the strains coming from feces contained 14 out of 16 virulence genes evaluated. Only 23% of the strains did not contain any of these genes. Conclusions A high percentage of feces and chicken meat samples are contaminated with C. jejuni. Moreover, these strains show a high genetic and phenotypic diversity represented by their antibiotic resistance profiles and the presence of virulence factors.

English

Epidemiologic and traceback evidence of Salmonella infection is not much in many developing countries including Burkina Faso. This study investigates the antimicrobial resistance and distribution of Salmonella serotypes isolated from diverse sources in Burkina Faso. 615 Salmonella serotypes isolated from beef meat, poultry carcasses, poultry, swine, cattle, hedgehog, fish, salad, channel and humans from 2009 to 2011 were analyzed to identify their diversity and distribution among the samples. The Salmonella strains were subjected to antimicrobial sensitivity tests using disk diffusion methods, were analyzed and classified into 110 serotypes, with the most prevalent serotype being Derby (91/615) found in beef meat, poultry carcasses, poultry and fish; Muenster (48/615) found in cattle, swine, hedgehog, poultry, human and fish; Chester (38/615) found in poultry carcasses, swine and poultry feces; Hato (32/615) found in beef meat, poultry carcasses, cattle and poultry; Drac (30/615) found in cattle, hedgehog and fish; and Typhimurium (21/615) found in cattle, poultry, human and fish. Among the 615 Salmonella strains, 94% (581/615) were resistant to one or more antibiotics; resistance to streptomycin was the most common. The resistance pattern, Str-Sul-Tet, Str-Tet and Str-Sul was dominant and found in 80% of the strains. About 3% of the strains were resistant to 5 or 6 antibiotics; their resistance pattern is amp-str-sul-tet-tmp or amp-chl-str-sul-tet-tmp. One Salmonella strain, S. Kentucky isolated from human stool was resistant to eight antibiotics; the resistance pattern is amp-str-sul-tet-cip-gen-nal-mec. Findings from this study can help define the guidelines for basic surveillance system of Salmonella and other enteropathogenic bacteria circulating among humans, animals, food and environment. Key words: Salmonella, environment, human, risk.

Quantitative detection of fecal contamination with domestic poultry feces in environments in China

Poultry are an important source of fecal contamination in environments. However, tools for detecting and tracking this fecal contamination are in the early stages of development. In practice, we have found that source tracking methods targeting the 16S rRNA genes of poultry-specific microbiota are not sufficiently sensitive. We therefore developed two quantitative PCR assays for detection of poultry fecal contamination, by targeting chicken and duck mitochondrial genes: NADH dehydrogenase subunit 5 (ND5) and cytochrome b (cytb). The sensitivity of both assays was 100% when tested on 50 chicken and duck fecal samples from 10 provinces of China. These assays were also tested in field samples, including soil and water collected adjacent to duck farms, and soils fertilized with chicken manure. Poultry mitochondrial DNA was detected in most of these samples, indicating that the assays are a robust method for monitoring environmental contamination with poultry feces. Complemented with existing indicators of fecal contamination, these markers should improve the efficiency and accuracy of microbial source tracking.

Nontyphoidal Salmonella Gastroenteritis in Baoshan, Shanghai, China, 2010 to 2014: An Etiological Surveillance and Case-Control Study

Nontyphoidal Salmonella (NTS) gastroenteritis is a widespread global foodborne disease. To identify the epidemiologic characteristics, sources of food contamination, and risk factors of NTS gastroenteritis, epidemiologic data and stool specimens of diarrheal patients were collected from sentinel hospitals in Baoshan, Shanghai, People's Republic of China, between 2010 and 2014. Food products from nearby farmers' markets and animal feces from live poultry markets and livestock farms were sampled to identify the pathogen; a case-control study was conducted to characterize risk factors of NTS gastroenteritis. Of 3,906 diarrheal patients examined, 266 (6.8%) were positive for Salmonella. The positive rates were higher in summer than in the other seasons. Salmonella Typhimurium (36.1%) and Salmonella Enteritidis (30.8%) were the dominant serovars in the patients. Salmonella was detected in 26.2% pork samples, 7.1 to 7.8% poultry meats, and 3.3 to 8.9% poultry feces. Salmonella Typhimurium was the major serovar in contaminated food and animal feces. Multivariate conditional logistic regression analysis indicated that consumption of pork and quickly cooked eggs increased, whereas separating kitchen knives for cooked and raw food decreased the risk of NTS gastroenteritis, independently. We believe that NTS in poultry feces contaminated the meat products in the same markets and then infected humans if these foods were not sufficiently cooked. To prevent NTS gastroenteritis, it is necessary to survey Salmonella in meats and poultry feces, to cook eggs and pork sufficiently, to separate kitchen knives for cooked and raw food, and to prohibit live poultry trade in fresh meat markets.

Development and application of an in-cell cleanup pressurized liquid extraction with ultra-high-performance liquid chromatography-tandem mass spectrometry to detect prohibited antiviral agents sensitively in livestock and poultry feces

An in-cell cleanup pressurized liquid extraction was developed to analyze prohibited antiviral agents in livestock and poultry feces. Extraction and cleanup were integrated into one step. The extraction was performed using methanol-acetonitrile (1:1, v/v) with 0.5% glacial acetic acid at 90°C, and 0.75g of PSA was used as the adsorbent during the extraction procedure. Under optimal conditions, the average recoveries for 11 antiviral drugs were 71.5–112.5% at three spiked levels (20, 40, and 100μgkg−1). The detection limits and detection quantitations of the analysis method for the eleven antiviral drugs were 0.6–1.4 and 1.4–4.7μgkg−1, respectively. Finally, the method was applied to analyze amantadine, oseltamivir and its metabolites oseltamivir acid in duck feces based on an experiment of an oral dose of two antiviral drugs in duck. The amantadine, oseltamivir and oseltamivir acid can be detected in feces within approximately four weeks after amantadine and oseltamivir were orally administered. The results indicate that the residue analysis in feces is a noninvasive method to monitor inhibited antiviral agents efficiently in livestock and poultry breeding.

Probiotic Potential of Lactic Acid Bacteria Isolated from Cheese, Yogurt and Poultry Faeces

Lactic acid bacteria are the most important bacteria that have been used as probiotic in food and feed industries. Due to their beneficial probiotic properties, research for new lactic acid bacterial strains is still continued for the new strains which are more tolerable to the stress conditions of the GIT, and have better probiotic properties than the existing strains. In the present study, a total of 33 isolates were obtained from yogurt, cheese and poultry faeces as a potential source for isolation of lactic acid bacteria. Based on the initial identification, 33 isolates which were most probably lactic acid bacteria were selected for in vitro acid and bile tolerance tests. Out of the 33 isolates, 13 isolates were subjected to acid and bile tolerance test and all of them showed good tolerance against acid and bile with more than 80% survival. Identification of 13 selected isolates which exhibited better acid and bile tolerance using 16S rRNA gene sequence analysis showed that all 13 isolates belonged to the genus Lactobacillus including seven L. paracasei, three L. Salivarious, one L. reuteri and one L. casei. Most of the isolates produced significant amount of organic acids, mainly lactic acid. Isolates were then subjected to the antibiotics resistance test and all of them were sensitive to most of the antibiotics except Vancomycin. All the isolated Lactobacillus strains showed good tolerance to acid and bile salts which indicates their survival ability in the GIT, and they might be considered as potential probiotic candidates for both humans and animals. Moreover, considering the production of considerable amounts of organic acids, these strains may have antagonistic activity against pathogenic strains. However, further studies are needed to investigate their probiotic properties including antimicrobial activity.

Isolation of rhamnolipids-producing cultures from faeces: Influence of interspecies communication on the yield of rhamnolipid congeners

The aim of this study was to evaluate the ability of bacterial cultures isolated from cattle, poultry or pig faeces and manure to produce rhamnolipids, as well as to investigate the influence of interspecies communication on possible quantitative differences in the production of rhamnolipid congeners. Initial screening methods (oil spreading, drop collapse, haemolytic activity and emulsification activity) showed that approximately 36% of the 51 isolated cultures exhibited the ability to produce biosurfactants. Subsequent studies using a selected culturable mixed culture (which included Enterococcus faecalis, Pseudomonas aeruginosa and Escherichia coli) revealed that only P. aeruginosa was able to produce this biosurfactant. HPLC–MS analysis showed that the surface active compounds were rhamnolipids. Further comparative studies confirmed that the total yield of rhamnolipids was notably higher in the bioreactor inoculated with the selected mixed culture (940.58±1.10mg/L) compared to the bioreactor inoculated with the axenic strain of P. aeruginosa (108.47±0.41mg/L). Twelve rhamnolipid congeners were identified during cultivation of the selected mixed culture, whereas six congeners were detected during cultivation of the sole axenic strain of P. aeruginosa. Furthermore, increased production of rhamnolipids was observed when the concentration of autoinducer molecules (AI-2) responsible for interspecies signaling increased, suggesting the influence of quorum-sensing communication on biosynthesis efficiency. This observation may be of importance for large-scale production of this biosurfactant, as it opens new possible solutions based on the use of mixed cultures or external addition of stimulating autoinducers.

English

Hydrolyzed proteins are used as attractive agents in McPhail traps for monitoring of fruit flies (Tephritidae). There has been no defined role for monitoring of insects belonging to the Lonchaeidae family. Currently, there is a great concern in using most efficient and low-cost attractive materials. Thus, this study aimed at assessing the attractiveness of solid and liquid baits in capturing of frugivorous flies (Tephritidae and Lonchaeidae). Therefore, we carried out four trials in coffee plantations (Coffea arabica L.) during two different periods (May/ 2013 and July/ 2014). A randomized block design with four treatments and five replications was used in the first period, and ten treatments with four replications the following year. Two distinct experiments were carried out, one using baits in solid and another in liquid form, which consisted of applying 10 g for trap (solid) or 200 mL solution of the same compounds diluted in water (5%: p/ v). In 2013, we tested yeast extract with and without sugar, brewer's yeast, citrus pulp and hydrolyzed protein as control. In 2014, five additional baits were tested: acai, plum and grape flours, passion fruit fiber and poultry feces. In all experiments, a 5% hydrolyzed protein solution was used as control. Eight days after being set, traps were assessed. Even the yeast extract, with and without sugar, and the brewer's yeast, in solid form, were as attractive as control treatment in capturing flies. The poultry feces and yeast extract, with and without sugar in solution form, can be used to replace hydrolyzed protein in capturing tephritids. Lonchaeids are barely attracted by the hydrolyzed protein. Additionally, yeast extract and poultry feces can be used for monitoring and biodiversity studies of the Lonchaeidae fauna. Key words: Fruit growing, monitoring, trap, protein.

Is Exposure to Poultry Harmful to Child Nutrition? An Observational Analysis for Rural Ethiopia.

Although strategic thinking on water, sanitation and hygiene (WASH) has prioritized reducing exposure to human feces in order to limit diarrheal infections, recent research suggests that elevated exposure to livestock–particularly poultry and poultry feces–may be an important risk factor for diarrhea, environmental enteric disorder (EED) and respiratory infections, all of which may seriously retard linear growth in young children. Yet a very different literature on nutrition-sensitive agriculture suggests that livestock ownership is highly beneficial for child growth outcomes through its importance for increasing consumption of nutrient-rich animal sourced foods, such as eggs. Together, these two literatures suggest that the net nutritional benefit of poultry ownership is particularly ambiguous and potentially mediated by whether or not children are highly exposed to poultry. We test this novel hypothesis using a large agricultural survey of rural Ethiopian households that includes measures of child height-for-age Z-scores (HAZ), ownership of poultry and other types of livestock, and an indicator of whether livestock are kept within the main household dwelling overnight. We used least squares regression analysis to estimate unadjusted and adjusted models that control for a wide range of potentially confounding factors. We find that while poultry ownership is positively associated with child HAZ [β = 0.291, s.e. = 0.094], the practice of corralling poultry in the household dwelling overnight is negatively associated with HAZ [β = -0.250, s.e. = 0.118]. Moreover, we find no negative associations between HAZ and corralling other livestock species indoors. These results suggest that while poultry ownership can be beneficial to child growth, overly close exposure to poultry poses a concurrent risk factor for undernutrition, most likely because of increased risk of infection.

Poultry Faeces Management by Bioconversion Technology with Modified GGC 2047 Model

&lt;p&gt;In this report, entitled “Poultry Faeces Management by Bioconversion Technology with Modified GGC 2047 model” focuses on various parameters relating to physico-chemical characteristics of the substrate, fertilizing value of digested poultry waste and potential to create profitability from biogas energy, thus generated and balancing the environmental aspects using poultry waste digestion. Also, biogas may be the tool of energy generation in rural areas while sanitation (waste management) in urban areas of developing countries asNepal. Biogas production from chicken faeces could be obtained more effectively by feeding around 8.5 kg per day. It is concluded that digester could be run by around 2.5 quintal chicken faeces per month. Hence those people, who can manage this quantity of waste, can utilize bio-digester without poultry farm.&lt;/p&gt;&lt;p&gt;&lt;em&gt;Journal of Advanced College of Engineering and Management, Vol. 1, 2015&lt;/em&gt;, pp. 107-117&lt;/p&gt;

Evaluation of potential probiotic characteristics and antibacterial effects of strains of Pediococcus species isolated from broiler chickens

Pediococcus spp. were isolated from poultry rectum, faeces and food as good probiotic candidates in order to select strains to be used as probiotic in poultry feed.A total of 168 lactic acid bacteria were isolated and 51 isolates including 31 Lactobacillus spp. and 20 Pediococcus spp. were able to survive in low pH and bile salt concentration. The Pediococcus spp. were identified and their ability to form biofilm, adhesion to Caco-2 cells and antimicrobial activities against enteric pathogenic bacteria were determined.The results showed the presence of two strains, Pediococcus acidilactici P17 and P19 in rectal swab samples from 21-d old chickens with significant antibacterial activities against Salmonella enteritidis and Escherichia coli.The results suggest that only a few isolates of Pediococcus with potential probiotic activities are present in the poultry industry.

Identification and prevalence of tetracycline resistance in enterococci isolated from poultry in Ilishan, Ogun State, Nigeria.

Background:Tetracycline is one of the most frequently used antibiotics in Nigeria both for human and animal infections because of its cheapness and ready availability. The use of tetracycline in animal husbandry could lead to horizontal transfer of tet genes from poultry to human through the gut microbiota, especially enterococci. Therefore, this study is designed to identify different enterococcal species from poultry feces in selected farms in Ilishan, Ogun State, Nigeria, determine the prevalence of tetracycline resistance/genes and presence of IS256 in enterococcal strains.Materials and Methods:Enterococci strains were isolated from 100 fresh chicken fecal samples collected from seven local poultry farms in Ilishan, Ogun State, Nigeria. The strains were identified by partial sequencing of 16S rRNA genes. Antibiotic susceptibility of the isolates to vancomycin, erythromycin, tetracycline, gentamicin, amoxycillin/claulanate, and of loxacin were performed by disc diffusion method. Detection of tet, erm, and van genes and IS256 insertion element were done by polymerase chain reaction amplification.Results:Sixty enterococci spp. were identified comprising of Enterococcus faecalis 33 (55%), Enterococcus casseliflavus 21 (35%), and Enterococcus gallinarium 6 (10%). All the isolates were resistant to erythromycin (100%), followed by tetracycline (81.67%), amoxicillin/clavulanic acid (73.33%), ofloxacin (68.33%), vancomycin (65%), and gentamicin (20%). None of the enterococcal spp. harbored the van and erm genes while tet(M) was detected among 23% isolates and is distributed mostly among E. casseliflavus. IS256 elements were detected only in 33% of E. casseliflavus that were also positive for tet(M) gene.Conclusion:This study provides evidence that tetracycline resistance gene is present in the studied poultry farms in Ilishan, Ogun State, Nigeria and underscores the need for strict regulation on tetracycline usage in poultry farming in the studied location and consequently Nigeria.

Prevalence and antimicrobial resistance pattern ofCampylobacterspecies among poultry and poultry handlers of Jammu

Campylobacter is one of the emerging zoonotic pathogens with poultry and their products serving as an important source of human infections. The present study was aimed to assess the prevalence of Campylobacter species among poultry and poultry handlers of R.S. Pura, Jammu and their antibiogram pattern. A total of 177 samples from poultry (n = 167) and poultry handlers (n = 10) were examined and 39 samples were found positive for Campylobacter species (32 C. jejuni, 6 C. coli and 1 C. lari). The prevalence of Campylobacter was 40.3, 13.2, 7.7 and 30.0% in poultry faeces, poultry meat, poultry carcass swabs and poultry handlers, respectively. Antimicrobial resistance pattern of C. jejuni and C. coli isolates was studied against nine antibiotics. Multidrug resistance among the isolates was found against ampicillin, metronidazole and cepholathin while high sensitivity was observed towards gentamicin, ciprofloxacin, furazolidone and tetracycline. The results of the present study indicate high prevalence of Campylobacter both in poultry and poultry handlers with varying in vitro sensitivity to different antibiotics. The outcome enunciates that appropriate control measures ensuring safety of poultry products and human health need to be devised.

Biology and description of immature stages of Gymnetis rufilateris (Illiger, 1800) (Coleoptera: Cetoniidae: Cetoniinae)

Abstract Larvae, pupae and adults of Gymnetis rufilateris (Illiger, 1800) (Coleoptera: Cetoniidae: Cetoniinae) were collected in the municipality of Rochedo, Mato Grosso do Sul State. Studies on biology and morphology were conducted at the Laboratory of Entomology of the Universidade Estadual de Mato Grosso do Sul in Aquidauana, Mato Grosso do Sul, Brazil. Females of couples formed in the laboratory oviposited and allowed the biology studies. The eggs lasted for 15.5 days. Larvae of the 1st, 2nd and 3rd instars lasted 13.5, 30.6 and 113.1 days, respectively. The pupal period lasted 12.8 days. The egg-to-adult period lasts 186.8 days. The larvae fed on decomposing feces of poultry. In the laboratory, adults fed on ripe banana (Musa sp.) (Musaceae). Descriptions of the 3rd larval instar and pupa of G. rufilateris are presented. A key to known larvae of Gymnetis is also included.

Surface modeling of soil antibiotics

Large numbers of livestock and poultry feces are continuously applied into soils in intensive vegetable cultivation areas, and then some veterinary antibiotics are persistent existed in soils and cause health risk. For the spatial heterogeneity of antibiotic residues, developing a suitable technique to interpolate soil antibiotic residues is still a challenge. In this study, we developed an effective interpolator, high accuracy surface modeling (HASM) combined vegetable types, to predict the spatial patterns of soil antibiotics, using 100 surface soil samples collected from an intensive vegetable cultivation area located in east of China, and the fluoroquinolones (FQs), including ciprofloxacin (CFX), enrofloxacin (EFX) and norfloxacin (NFX), were analyzed as the target antibiotics. The results show that vegetable type is an effective factor to be combined to improve the interpolator performance. HASM achieves less mean absolute errors (MAEs) and root mean square errors (RMSEs) for total FQs (NFX+CFX+EFX), NFX, CFX and EFX than kriging with external drift (KED), stratified kriging (StK), ordinary kriging (OK) and inverse distance weighting (IDW). The MAE of HASM for FQs is 55.1μg/kg, and the MAEs of KED, StK, OK and IDW are 99.0μg/kg, 102.8μg/kg, 106.3μg/kg and 108.7μg/kg, respectively. Further, RMSE simulated by HASM for FQs (CFX, EFX and NFX) are 106.2μg/kg (88.6μg/kg, 20.4μg/kg and 39.2μg/kg), and less 30% (27%, 22% and 36%), 33% (27%, 27% and 43%), 38% (34%, 23% and 41%) and 42% (32%, 35% and 51%) than the ones by KED, StK, OK and IDW, respectively. HASM also provides better maps with more details and more consistent maximum and minimum values of soil antibiotics compared with the measured data. The better performance can be concluded that HASM takes the vegetable type information as global approximate information, and takes local sampling data as its optimum control constraints.

Campylobacter species isolated from poultry and humans, and their analysis using PFGE in southern Brazil

Campylobacteriosis is a bacterial disease transmitted to humans through ingestion of contaminated food. Six hundred samples were collected, 200 from human stool samples, 200 from poultry products and 200 from poultry feces in Southern Brazil, and then inoculated on blood agar plates. A total of 58% of the poultry feces, 17% of the poultry meat, and 2% the of human stools tested positive for Campylobacter. Positive Campylobacter colonies were identified as Campylobacter jejuni or Campylobactercoli by multiplex PCR. Campylobacter isolates were analyzed using PFGE to compare different profiles according to the source. This study demonstrated that there are different Campylobacter clones distributed in different aviaries in Southern Brazil. In addition, PFGE molecular profiles suggested that broilers can be a source of contamination of poultry products. However, the human isolate studied did not show any relationship with other strains examined.

Characterization of Candida famata Isolated from Poultry Feces for Possible Probiotic Applications

We studied here the yeast content of poultry feces, collected randomly from a French farm located in the north of the country. Thus, 81 yeast colonies were isolated and clustered into 22 distinct groups using the rep-PCR method. A single colony was taken from each group and identified using biochemical (ID 32C system) and molecular (sequencing of the D1/D2 domain of 26S rDNA and ITS1-5.8-ITS2 rDNA region) methods. Both methods led to the identification of Candida famata species. One isolate of C. famata strains, named strain Y5, was further studied for its cytotoxicity, adhesion, and surface properties, hemolytic activity, and its survival in simulated gastric and intestine environments. The data obtained advocate the probiotic potential of this isolate.