Soil survival of Salmonella and transfer to freshwater and fresh produce

An increase in human outbreaks caused by Salmonella sp. has been recognised in many parts of the world. Outbreaks are increasingly related to consumption of fresh produce and an understanding of soil survival of Salmonella and transfer to water and to fresh produce are needed to control salmonellosis. The increase in outbreaks is most likely associated with better surveillance, greater consumer demand and a change in production and distribution. This review summarises the recent literature of the ecology of Salmonella sp. in soil environment including sources, survival, transport and crop contamination. Areas with a high density of animal production are recognised as a high risk for contaminating fresh produce, however the specific path of contamination remains unconfirmed. Suspected sources include improperly composted manure/wastewater, the use of irrigation water in the vicinity of animal production and wild animals.Once introduced to the soil the survival of Salmonella sp. has been shown to be influenced by method of introduction, temperature and predation by soil protozoa amongst others. Detection of Salmonella in environmental samples is traditionally measured by classical growth dependent methods — these methods are discussed and although the new molecular based techniques still lack sensitivity compared to the classic techniques new possibilities are constantly emerging such as mRNA of the Salmonella invA gene directly in soil.Salmonella sp. can be transferred to fresh water either through the preferential flow paths of the soil or in the surface run-off water. In addition to soil properties this transport is influenced cell properties such as size, electric charge and hydrophobicity.The contamination of fresh produce is finally shown to follow several different routes including sprinkling and water splashes during rain events, the fresh produce can be contaminated by cells attached to the surface or by internal colonisation of the plant cells.     

Prevalence and serovars of Salmonella enterica on pig carcasses,slaughtered pigs and the environment of four Spanish slaughterhouses

The purpose of this study was to investigate the prevalence of Salmonella contamination and main serovars in pig slaughterhouses in Spain including carcasses, live animals and the environment. A total of 896 pig carcasses were randomly selected and swabbed before chilling in 3–5 visits to four pig slaughterhouses (A, B, C and D). Salmonella contamination was detected in 39.7% of the carcasses. The prevalence of positive carcasses was similar amongst slaughterhouses but significant differences were observed when taking sampling day into consideration within each of the slaughterhouses. Furthermore, a significant reduction in the prevalence of Salmonella contaminated carcasses (10.8%) was demonstrated in slaughterhouses C and D after chilling and cooling procedures.Sixteen batches of 10 animals were tracked from farm-to-slaughterhouse in slaughterhouses A and B to investigate the relationship between carcass contamination and contamination in live animals entering the slaughterhouse. No difference was found between infected and uninfected animals with respect to Salmonella contamination of the carcass although an increase in Salmonella contamination during the processing of live pigs into pork carcasses was evident. Regarding contamination in the slaughterhouse environment, Salmonella was isolated from most of the evaluated points in the slaughter line of the four studied slaughterhouses. Holding pens were identified as highly contaminated and what is more the ineffectiveness of the routinely cleaning protocols at this level was demonstrated in slaughterhouses C and D.The predominant Salmonella serovars found in carcasses, live pigs entering the slaughterhouse and the environment of the slaughterhouse were S. Typhimurium, S. Rissen, S. Derby and S. 4,[5],12:i:-. The same serovars were found in all the stages supporting the hypothesis that infected pigs are the main source of Salmonella contamination within slaughterhouses.     

Spices and herbs as source of Salmonella-related foodborne diseases

Salmonella is a leading cause of foodborne diseases and the role of ready-to-eat products including plant-derived food is increasingly recognized. The present survey reviewed recent literature on Salmonella-related outbreaks caused by spices and herbs and on the occurrence of Salmonella in these food matrices. Spices and herbs contaminated with Salmonella were responsible for a variety of foodborne outbreaks in Europe and North America. Identified serovars did often not belong to those predominating in human illness. Moreover, in different survey studies, Salmonella belonging to a broad diversity of serovars were found in a variety of spices and herbs. The proportion of Salmonella-positive samples ranged from 0% to 8.4%, albeit detection rates were rather low in most studies. Higher prevalence rates were often obtained with regard to a specific spice or herb type. Due to high desiccation tolerance, Salmonella can survive for an extended period of time in spices and dried herbs. Thus, by the use of untreated spices and herbs for production of foods not subjected to a heat treatment or for seasoning of ready-to-eat products, Salmonella might be introduced and in this way might pose a threat to consumers.     

Introduction of new multidrug-resistant Salmonella enterica strains into commercial dairy herds

A longitudinal observational study of 59 dairy herds was conducted in Washington State to estimate the rate of introduction of new multidrug-resistant (MDR) Salmonella enterica strains onto commercial dairy herds. Samples were collected on these herds over 7 visits separated by intervals of 2 to 4 mo over a period of 15 to 21 mo. Samples were cultured for Salmonella spp. and serogroup, serovar, and antimicrobial susceptibility patterns were identified for MDR Salmonella isolates. Fingerprinting generated by pulsed-field gel electrophoresis (PFGE) using XbaI restriction enzyme digestion generated genotyping profiles for all MDR isolates identified in the study. The rate of new MDR Salmonella strain introduction was 0.9 per herd-year (95% confidence interval: 0.6-1.4). The rates for the most commonly introduced MDR Salmonella serovars were 0.4/herd-year for Typhimurium, 1.2/herd-year for Newport, and 0.1/herd-year for Dublin. Thirty-three of 59 herds (56%) had at least one new MDR Salmonella introduction during the study period. The number of new MDR Salmonella strains acquired by dairy herds ranged from zero to 8. Thirteen of the 59 herds had a history of clinical salmonellosis. Among these 13 herds, 6 herds acquired new MDR Salmonella strains, although these strains were different than historical clinical strains. These data indicate that acquisition of new MDR Salmonella strains by dairy herds was a common event in participating herds, although the number of strains introduced varied greatly among herds.     

Salmonella status of pigs at slaughter--bacteriological and serological analysis

Apart from Salmonella monitoring of pig herds during the period of growth to evaluate the efficacy of control programmes, monitoring at harvest level is of relevance to assess the Salmonella status of fattening pigs and the associated risk of introducing Salmonella organisms in the slaughter process. Samples from 1830 fattening pigs were gathered at slaughter. Ileocaecal lymph nodes, rectal and caecal content as well as tonsils were collected for bacteriological examinations, and a part of the diaphragm pillar muscle was taken to gain meat-juice for serological analysis. Salmonella spp. was recovered from 13.8% of all pigs examined. Salmonella Typhimurium and Derby were the dominating serovars. The highest detection rates were found in caecal content followed by ileocaecal lymph nodes. By analysing both organs nearly 90% of all Salmonella positive pigs could be identified. Serological examination revealed 9.6% of the pigs as positive using a cut-off value of OD % ≥ 40. Only one quarter of all Salmonella positive pigs showed also a positive serological result. A reduction of the cut-off value does not necessarily result in a higher compliance between bacteriologically and serologically positive slaughter pigs. Detection of antibodies is useful to verify whether pig herds were previously exposed to Salmonella organisms. However, the Salmonella status of pigs at time of slaughter and the associated risk of dissemination of Salmonella organisms can only be assessed by bacteriological examinations which should include both lymph nodes and caecal content.     

Building PulseNet Latin America and Caribbean Salmonella regional database: First conclusions of genetic subtypes of S. Typhi,S. Typhimurium and S. Enteritidis circulating in six countries of the region

PulseNet Latin America and Caribbean Network (PulseNet LA and C) works together with PulseNet International sharing molecular epidemiologic information for the recognition and investigation of foodborne disease outbreaks.The participants of PulseNet LA and C perform standardized pulsed field gel electrophoresis (PFGE) protocols and analysis generating data that is incorporated into Regional Databases. In this study we present the relationship and distribution of genetic subtypes of Salmonella enterica ser. Typhimurium (STM), Salmonella enterica ser. Enteritidis (SE), and Salmonella enterica ser. Typhi (ST) human isolates circulating in six countries of the Region between 2005 and 2009, from the analysis of the Salmonella Database.The 70 ST isolates analyzed were diverse and none of the countries shared the same PFGE profiles with XbaI enzyme. These results show a high genetic diversity among the strains studied and provide background to trace future outbreaks and travel related cases. In the analysis of 550 STM isolates, we found 10 patterns shared at least between two countries, suggesting the need of further studies of attribution to the source of origin. Only one of these PFGE patterns was associated with a known outbreak. Among 225 SE isolates, a predominant subtype was identified, that grouped 83.5% of the isolates and was associated with foodborne outbreaks in five of the six countries; showing the need to use other subtyping techniques for this serovar.The continuous update of PulseNet LA and C Salmonella Regional Database provides an important tool for the laboratory based surveillance of the serovars analyzed, for the prevention and control of foodborne outbreaks, and for the detection of emerging strains in the Region.     

Salmonella serovars isolated from table eggs: An overview

Salmonellosis can be acquired through consumption of infected raw or undercooked eggs. The European Commission has set criteria to control Salmonella Enteritidis (SE) and Salmonella Typhimurium (ST) infections in laying flocks, to reduce the risk of contaminated eggs entering the food chain. SE is considered the serovar mostly implicated in Salmonella egg related food poisoning, for its peculiar ability to contaminate the egg contents through vertical transmission. Other Salmonella serovars (SO) and ST generally contaminate eggs externally, and are found in the egg contents following penetration through the eggshell. A review of the information available on egg contamination by SE, ST and SO is presented, followed by a collation of the surveys investigating table egg contamination at retail. Where available, information on the serovars identified in these surveys and Salmonella contamination of the egg (shell, contents or both) is detailed. SE appears to play a major role in egg contamination. Isolation of ST from eggs is not frequent, and appears to be mostly on the eggshells. In the majority of the studies, more samples were positive for SO than for ST. In some studies, one individual serovar exceeded ST. The data presented in this article shows how ST is not often isolated from table eggs and that contamination of table eggs with SE and SO is more frequent.     

Multiplex TaqMan® detection of pathogenic and multi-drug resistant Salmonella

Overuse of antibiotics in the medical and animal industries is one of the major causes for the development of multi-drug-resistant (MDR) food pathogens that are often difficult to treat. In the past few years, higher incidences of outbreaks caused by MDR Salmonella have been increasingly documented. The objective of this study was to develop a rapid multiplex real-time polymerase chain reaction (PCR) assay for simultaneous detection of pathogenic and MDR Salmonella spp. A multiplex TaqMan®real-time PCR was designed by targeting the invasin virulence gene (invA), and four commonly found antibiotic resistance genes, viz. ampicillin, chloramphenicol, streptomycin and tetracycline. To avoid false negative results and to increase the reliability of the assay, an internal amplification control (IAC) was added which was detected using a locked nucleic acid (LNA) probe. In serially diluted (5 ng–50 fg) DNA samples, the assay was able to detect 100 genomic equivalents of Salmonella, while in a multiplex format, the sensitivity was 1000 genomic equivalents. The assay performed equally well on artificially contaminated samples of beef trim, ground beef of different fat contents (73:27, 80:20, 85:15 and 93:7), chicken rinse, ground chicken, ground turkey, egg, spinach and tomato. While the detection limit for un-enriched inoculated food samples was 10⁴ CFU/g, this was improved to 10 CFU/g after a 12-h enrichment in buffered peptone water, with 100% reproducibility. The multiplex real-time assay developed in this study can be used as a valuable tool to detect MDR virulent Salmonella, thus enhancing the safety of food.     

Salmonella Typhimurium general virulence factors: A battle of David against Goliath?

The genus Salmonella is the most common agent causative of foodborne diseases. Although genus Salmonella members are genetically close microorganisms, they show wide variations in host-specificity, virulence and disease manifestations. Salmonellosis caused by contaminated water or food is usually present as two clinical forms: typhoid fever and nontyphoidal diseases. The latter producing gastroenteritis is frequently caused by Salmonella Typhimurium and Salmonella Enteritidis. The nontyphoidal S. Typhimurium infection involves the following steps: bacterial adhesion, invasion, SCV maturation and replication. During these steps there is a strong interaction between host and pathogen, in which the pathogen must resist different host defense mechanisms. In each of these stages the bacteria modulate the expression of diverse groups of genes, most of which are encoded in Salmonella pathogenicity islands (SPI). This modulation is in general under control of the so-called two-component systems (TCS). The TCSs are capable of sensing different environmental conditions and trigger a physiological response. Currently, the risk of contracting salmonellosis disease has been considerably increased due to the emergence of new serovars showing multiple-drug resistance that presents a high risk to human health. In this work, we summarize the new advances in the study of host–pathogen interactions during the Salmonella infection that leads to the establishment of the disease. This finding highlights the role of the S. Typhimurium secretion systems and effectors during infection. In addition, we mentioned some strategies that could be explored in order to take control of Salmonella infections.     

Prevalence and antibiotic resistance of Salmonella serovars in ducks,duck rearing and processing environments in Penang,Malaysia

An investigation was carried out to determine the prevalence and antibiotic resistance of Salmonella serovars in ducks, their rearing and processing environments in Penang, Malaysia. A total of 531 samples collected from wet markets and duck farms, were examined from August 2009 to October 2010. The overall prevalence of Salmonella serovars was 23.5% (125/531). The 125 Salmonella isolates belong to 10 different serovars namely Typhimirium (29.6%), Enteritidis (12.0%), Gallinarum (2.4%), Braenderup (12.0%), Albany (11.2%), Hadar (20.8%), Derby (6.4%), Weltevreden (1.6%), Newbrunswick (3.4%) and London (0.8%). Salmonella serovars also showed various resistance patterns against 13 different antibiotics. All the serovars were resistant to erythromycin but susceptible to cephalothin, gentamicin and ceftriaxone. Plasmids were detected in 91 (72.8%) of the isolates with sizes ranging from 1.4 to 23.1 Kbp. Our findings provide baseline information on the distribution of Salmonella serovars in ducks, their rearing and processing environments, and indicate that ducks should be considered as an important source of food-borne pathogens.     

Incidence and role of Salmonella in seafood safety

Seafood products are appreciated worldwide for their high nutritional value and are increasingly popular among consumers. Consumer preferences range from fresh products, eaten raw or minimally processed, to variously prepared (salted, smoked, cured, canned) and ready-to-eat (RTE) products. Moreover, seafood products are a major food category in international trade and are frequently shipped very long distances. All these factors expose seafood to various contaminants, including those of microbiological origins, such as Salmonella. The presence of Salmonella in seafood may derive from contamination occurring in the natural aquatic environment, in aquaculture or during processing. In addition, the isolation of Salmonella serovars that are resistant and multiresistant to antibiotics continues to raise concerns. In this review various aspects associated with the microbiological risk posed by the presence of Salmonella in seafood are examined. The most recent data of incidence are presented, and some prevention and control strategies are considered.     

Incidence and antibiotic resistance of Salmonella spp. on raw chicken carcasses

The current study was carried out to detect Salmonella spp. contamination on chicken carcasses and to determine the antibiotic susceptibility profiles and serotype distribution of the isolates. A total of 200 packaged fresh raw chicken samples sold at retail in different markets in central Anatolia were analysed between April 2005 and March 2006. Salmonella spp. was detected in 34% (68/200) of samples using cultural technique and were confirmed by PCR. Ten Salmonella serovars were identified; predominant ones included Typhimurium, Infantis and Heidelberg. All of the Salmonella spp. isolates tested, exhibited resistance to one or more antimicrobial agents used. Resistance to penicillin, oxacillin, clindamycin, vancomycin, erythromycin and ampicillin were evident 100%, 97%, 97%, 92.6%, 89.7% and 85.2%, respectively. Also resistance to tetracycline (67.6%), streptomycin (61.7%), neomycin (55.8%) and cephalothin (52.9%) was observed but a small percentage of the isolates demonstrated resistance to gentamicin (14.7%), chloramphenicol (10.2%), cefotaxime (2.9%) and amikacin (2.9%). As a result, high prevalence of Salmonella spp. and the relatively high resistance among the bacteria tested could pose public health and therapeutic problems in consumers as potential vehicle of resistant Salmonella foodborne infections. To avoid Salmonella contamination, hygienic rules of slaughter and poultry meat processing must be rigorously observed and antibiotic use must be controlled by governmental agencies to prevent increased resistance of antibiotics.     

Short communication: Determination of Salmonella clustered regularly interspaced short palindromic repeats (CRISPR) diversity on dairy farms in Wisconsin and Minnesota

Salmonella enterica ssp. enterica is a foodborne pathogen able to cause disease in both humans and animals. Diverse serovars of this pathogen exist, some of which are host specific, causing a range of clinical symptoms from asymptomatic infection through morbidity and mortality. According to a 2007 survey by the USDA National Animal Health Monitoring System, fecal shedding of Salmonella from healthy cows occurs on 39.7% of dairy farms in the United States. Certain serovars are frequently isolated from dairy farms and the majority of isolates from the National Animal Health Monitoring System study were represented by 5 serovars; however, genotypic diversity was not examined. The objective of this study was to determine the diversity of clustered regularly interspaced short palindromic repeats (CRISPR) loci in Salmonella collected from 8 dairy farms with a previous history of salmonellosis. None of the cows or calves sampled on 2 of the 8 dairy farms were shedding Salmonella, although Salmonella was detected in a cow bedding sample on 1 of these farms. Salmonella populations were discrete on each farm, according to CRISPR typing, with the exception of an Anatum var. 15+ type on farms 5 and 6 and the Montevideo type on farms 1 and 2. One to 4 distinct CRISPR genotypes were identified per farm. The CRISPR typing differed within serovars, as Montevideo, Anatum var. 15+, and Muenster serovars had no overlap of spacer content, even on the same farm, reflecting between- and within-serovar genetic diversity. The dynamic nature of Salmonella populations was shown in a farm that was sampled longitudinally over 13.5 mo. Changes in serovar from 3,19:-:z27 to Montevideo was observed between the first sampling time and 8 mo later, with concomitant change in CRISPR alleles. The results indicate that Salmonella strains present in smaller dairy herds (<500 head) are specific to that farm and new Salmonella strains may emerge over time.     

Salmonella spp. in low water activity food: Occurrence,survival mechanisms,and thermoresistance

The occurrence of disease outbreaks involving low-water-activity (a_w) foods has gained increased prominence due in part to the fact that reducing free water in these foods is normally a measure that controls the growth and multiplication of pathogenic microorganisms. Salmonella, one of the main bacteria involved in these outbreaks, represents a major public health problem worldwide and in Brazil, which highlights the importance of good manufacturing and handling practices for food quality. The virulence of this pathogen, associated with its high ability to persist in the environment, makes Salmonella one of the main challenges for the food industry. The objectives of this article are to present the general characteristics, virulence, thermoresistance, control, and relevance of Salmonella in foodborne diseases, and describe the so-called low-water-activity foods and the salmonellosis outbreaks involving them.     

Application of a bacteriophage cocktail to reduce Salmonella Typhimurium U288 contamination on pig skin

Multidrug-resistant Salmonella Typhimurium U288 is a significant pathogen of pigs, accounting for over half of all outbreaks on UK pig production premises. The potential of this serovar, and other salmonellae, to enter the food chain during the slaughtering process requires that efforts be made to reduce the prevalence of these bacteria at both the pre- and post-harvest stages of production. A bacteriophage cocktail (PC1) capable of lysing various Salmonella enterica serovars was designed using the broad host-range phage Felix 01, and three phages isolated from sewage. PC1 applied to pig skin experimentally-contaminated with U288 achieved significant reductions (P < 0.05) in Salmonella counts when stored at 4 °C over 96 h. Reductions of > 1 log₁₀ unit were observed when the ratio of phage applied was in excess of the bacterial concentration. The treatment was found to be effective at a multiplicity of infection (MOI) of 10 or above, with no significant reductions taking place when the MOI was less than 10. Under these conditions U288 counts of log₁₀ 4.1-4.3 CFU were reduced to undetectable levels following the application of PC1 to pig skin (> 99% reduction). These data suggest phage cocktails could be employed post-slaughter as a means to reduce Salmonella contamination of pig carcasses.     

Prevalence, distribution, and molecular characterization of Salmonella recovered from swine finishing herds and a slaughter facility in Santa Catarina, Brazil

Swine can carry Salmonella strains that may be transmitted to humans by pork products. This investigation determined the distribution and types of Salmonella in 12 swine finishing herds and a slaughter facility in Santa Catarina, Brazil. A total of 1258 samples, consisting of environmental, feed, carcass, lymph node, and fecal material were collected and submitted to bacteriological isolation of Salmonella. From 487 positive samples, 1255 isolates were recovered and confirmed to be Salmonella. The distribution of positive samples was as follows: finishing pen floors 26% (16/61); feed 29% (42/143); feces 44% (52/119); pooled feces 59% (35/59); slaughter holding pens 90% (36/40); lymph nodes 46% (220/478); pre-chilled carcass surfaces 24% (24/98); and post-chilled carcass surfaces 24% (62/260). The most prevalent serovars were Typhimurium, Panama, Senftenberg, Derby, and Mbandaka. By pulsed-field gel electrophoresis, 1071 isolates were subtyped using XbaI, and duplicate isolates were removed. From the remaining 747 isolates, 163 macrorestriction profiles (pulsotypes) were identified. Six pulsotypes were considered very frequent, occurring in 33 isolates or more. The multiple correspondence analyses showed correlations between pulsotypes from shedding pigs (feces), herd environment (pen floors), and subiliac and prescapular lymph nodes and between lairage and carcass surface samples before and after chilling. All sources of Salmonella investigated contributed to the carrier state; however, pre-slaughter contamination at lairage was the variable most strongly associated with carcass contamination. A total of 59 different antimicrobial resistance profiles were observed in 572 Salmonella isolates. From these isolates, 17% (97/572) were susceptible to all 15 antibiotics tested, 83% (475/572) were resistant to at least one, and 43% (246/572) were resistant to four or more antibiotics (multi-resistant). The AmpGenKanTet profile was the most prevalent in carcass isolates and was associated with farm origin.     

Examination of the internalization of Salmonella serovar Typhimurium in peanut,Arachis hypogaea,using immunocytochemical techniques

A variety of products of plant origin, such as tomatoes, melons, peppers, and peanuts, have been implicated in Salmonella spp. associated outbreaks in recent years. Although these bacteria have been found to internalize within some plants associated with foodborne-related outbreaks, the internalization in peanut plants has not been examined to date. To investigate internalization and where the bacteria localize within the plant, intact peanut seeds were contaminated with Salmonella serovar Typhimurium expressing green fluorescent protein (GFP) for 30 min and immunocytochemical techniques were used to localize the bacterium within the stem tissue of 16 day-old peanut plants. An average of 13.6 bacteria/mm³ were localized within the sampled tissue. The bacteria were found to be associated with every major tissue (cortical, vascular, epidermal, and pith) and corresponding cell type. The cortical cells located to the outside of the vascular bundles contained the majority of the Salmonella cells (72.4%). Additional growth experiments demonstrated peanut seedlings could support the reproduction of Salmonella to high levels (10⁹ CFU/plant) after 2 days following seed contamination. Together these results show that Salmonella Typhimurium can internalize within many different plant tissue types after a brief seed contamination event and that the bacteria are able to grow and persist within the plant.     

Impact of the Australian litter re-use practice on Salmonella in the broiler farming environment

This study has examined the dynamics (in terms of levels and serovar diversity) of Salmonella in the “dual litter environment” that occurs within a single shed as a result of a management practice common in Australia. The study also looked at the physical parameters of the litter (pH, moisture content, water activity and litter temperature) as a means of understanding the Salmonella dynamics in these litter environments. The Australian practice results in the brooder end of the shed having new litter each cycle while the grow-out end has re-used litter (a “dual litter environment”). Two farms that adopted this partial litter re-use practice were studied over one full broiler cycle each. Litter was sampled weekly for the levels (and serovars) of Salmonella during a farming cycle. There was a trend for lower levels of Salmonella (and a lower Salmonella serovar) diversity in the re-used litter environment as compared with the new litter environment. Of the physical parameters examined, it would appear that the lower water activity associated with the re-used litter may contribute to the Salmonella dynamics in the dual environment.     

Serodiversity and serological as well as cultural distribution of Salmonella on farms and in abattoirs in Lower Saxony, Germany

In this study fattening pigs were monitored on farms and in the abattoir for Salmonella prevalence. The samples with the highest prevalence at slaughter should be identified with special attention to the distribution of Salmonella serovars on farms in comparison to those in slaughtered pigs. Another aim was to monitor whether high serological antibody responses in pigs are in accordance with the specific Salmonella serovars in tissues. From 3418 farm faecal samples, 191 were Salmonella positive (5.58%), whereas from slaughtered pigs 330 out of 2494 analysed samples were Salmonella positive (13.2%) with the highest prevalence in the caecal content (124/499 = 24.9%). The chi-square test for homogeneity between the serovars found on farms and in the different types of samples at slaughter was in most cases negative (p < 0.05). Exceptions were the similar serovars found in samples taken from farm 1 and in the corresponding ileocaecal lymph nodes extracted at slaughter (p = 0.1188); in samples taken from farm 2 and the corresponding tonsils (p = 0.1479) and in samples taken from farm 3 and the corresponding caecal content (p = 0.3230) and ileocaecal lymph nodes (p = 0.1921), respectively. The frequency distribution in different samples was significantly different in most cases. Three exceptions, the distribution between tonsils and caecal content among antibody titre in meat juice (cut off 40) and cultural detection of Salmonella spp. in ileocaecal lymph nodes, as well as between meat juice samples (cut off 20) and caecal content did not differ significantly. The Kappa indices only showed signs of weak concordance according to positive test results (Kappa ≤ 0.4) between different sample types on an animal basis. Pigs harbouring S. Typhimurium 1,4,12:i:1,2; DT104L in tonsils or S. Typhimurium 1,4,12:i:1,2 DT 104B low in caecal content or ileocaecal lymph nodes had the highest optical densities in meat juice. Apart from the different Salmonella prevalences between farms and slaughterhouses and in most cases nonexisting concordance in Salmonella serovar distribution on farms and at slaughter, also in future farm intervention strategies to control Salmonella in the food chain are not dispensable. This is because once introduced into a slaughterhouse via swine the serovars seem to maintain the resident slaughterhouse flora and add to it.     

Short communication: Characterization of Salmonella phages from dairy calves on farms with history of diarrhea

Salmonella enterica can cause disease and mortality in calves. This pathogen is also a zoonosis that can be transmitted by animal contact or by food. The prevalence of Salmonella in dairy farms has been reported to range from 0 to 64%, and, due to the diversity of Salmonella serovars that can be circulating, Salmonella is an important concern for dairy production. Bacteriophages that infect Salmonella have been documented to be abundant and widely distributed in the dairy environment. The current study investigated the diversity of Salmonella serovars and Salmonella phages in 8 dairy farms with a history of diarrhea in southern Chile. A total of 160 samples from sick calves, healthy calves, and the environment were analyzed for Salmonella and phage. Isolated phages were characterized and classified by their host range using a panel of 26 Salmonella isolates representing 23 serovars. Host ranges were classified according to lysis profiles (LP) and their spatial distribution was mapped. Salmonella-infecting phages were identified, but none of the 160 samples were positive for Salmonella. A total of 45 phage isolates were obtained from sick calves (11), healthy calves (16), or the environment (18). According to their host range, 19 LP were identified, with LP1 being the most common on all 8 farms; LP1 represents phages that only lyse serogroup D Salmonella. The identification of Salmonella phages but not Salmonella in the same samples could suggest that these phages are controlling Salmonella in these farms.