Hemolytic Bacteria Research Articles

The role of open-air inhalatoria in the air quality improvement in spa towns

The present study was aimed at evaluating microbiological contamination of air in Ciechocinek and Inowrocław - Polish lowland spa towns. Additionally, the impact of open-air inhalatoria on the quality of air was evaluated. Air samples were collected seasonally in the urban areas, in the recreation areas and in the vicinity of inhalatoria in both towns using impaction. The numbers of mesophilic bacteria, staphylococci, hemolytic bacteria and actinomycetes were determined on media according to the Polish Standard PN-86/Z-04111/02. The number of moulds was determined on media according to the Polish Standard PN-86/Z-04111/03. While the highest numbers of microorganisms were noted at the sites located in the urban areas, the lowest numbers were noted in the vicinity of the open-air inhalatoria. In all the investigated air samples the values of bioaerosol concentrations were below the recommended TLVs (≤ 5000 CFU×m(-3) for both bacteria and fungi in outdoor environments). Location of the sampling site was invariably a decisive factor in determining the number of microorganisms in the air. The aerosol which is formed in the open-air inhalatoria has a positive influence on microbiological air quality. Owing to a unique microclimate and low air contamination, Ciechocinek and Inowrocław comply with all necessary requirements set for health resorts specializing in treating upper respiratory tract infections.

Municipal landfill sites as sources of microorganisms potentially pathogenic to humans

The present research was aimed at assessing the quality of air and soil on the premises and in the vicinity of the municipal landfill sites in Toruń with regard to the presence of pathogenic bacteria, potentially dangerous to humans. Air samples (the impaction method using a MAS-100 impactor) and soil samples were collected from seven sampling sites including the operating and closed landfill cells, sampling sites located near leachate ponds, and sampling sites located outside the above premises. The research also involved assessing microbial air contamination in three indoor spaces on the premises of the landfill sites. Microbial tests involved the determination of the number of culturable mesophilic, mannitol-positive, and α- and β-hemolytic bacteria in the air, determination of the number of coliform bacteria, spore-forming Clostridium perfringens in soil, and the presence of Salmonella in soil. The results indicate that bioaerosol emitted by this municipal facility is the source of hemolytic bacteria (≤ 300 CFU m(-3) of air), as well as of pathogenic bacteria (Pseudomonas aeruginosa and Bacillus subtilis). The highest risk of exposure to biological agents was determined in the sorting facility. Over sixty percent of air samples in this sampling site presented high pollution degree with mesophilic bacteria (500-2000 CFU m(-3) of air) and over one fourth of air samples presented very high pollution degree (>2000 CFU m(-3) of air). Indoor air in other rooms was considered highly/moderately contaminated (100-2000 CFU m(-3) of air). The highest risk related to the presence of Salmonella, Clostridium perfringens, and coliform bacteria in soil was determined at the operating landfill cell and near the leachate pond of the closed landfill cell. At the operating landfill cell the total coli ranged from 4-1226 MPN g(-1) of dry mass of soil and Clostridium perfringens ranged from <LOD-1604 CFU g(-1) of dry mass of soil. The results question the strategy of municipal landfill sites in densely populated areas, and emphasize the need for regular monitoring of microbiological tests in their vicinity as well as for control strategies in order to protect workers at landfill sites. The results of the study should be used for future decisions on the location of municipal landfill sites and suggest the need for better environmental control technologies in the sites that are already functioning.

An aerolysin‐like enterotoxin from Vibrio splendidus may be involved in intestinal tract damage and mortalities in turbot, Scophthalmus maximus (L.), and cod, Gadus morhua L., larvae

Vibrio splendidus is a pathogen that can cause major losses during the early stages of larval turbot rearing when live feed (rotifers or Artemia) is used. As haemolytic bacteria have often been associated with larval rearing losses, we studied the role of the V. splendidus haemolysin in infection of larvae. From a bank of over 10,000 transposon mutants of V. splendidus, two different types of haemolysin-negative mutants were obtained. Both had lost virulence for larval fish, and immunohistochemistry showed that the transposon mutant studied colonized the turbot larval intestinal tract at a similar level to the wild-type organism but did not cause damage or signs of enteritis found with the wild-type organism. One transposon insertion site was located within a gene with high homology to aerolysin, the cytolytic toxin produced by several Aeromonas spp. The haemolysin, which we have termed vibrioaerolysin, had properties similar to aerolysin and osmotic protection studies showed that it formed pores in the membranes of erythrocytes of similar diameter to those of aerolysin. The Tn10 insertion site of the second transposon mutant was in an adjacent ToxR-like gene, suggesting that this might control expression of the vibrioaerolysin. The gastroenteritis caused by Aeromonas spp. in humans is considered to be due to production of aerolysin causing cyclic AMP-dependent chloride secretion in cells of the gastrointestinal tract. Damage to the intestinal tract of marine fish larvae could occur in a similar way, and it is possible that several Vibrio spp. found in the developing bacterial flora of the larval fish gut can secrete aerolysin-like toxins leading to death of larvae in the early rearing stages. Routine bacteriological screening on blood agar plates of live feed is recommended with measures to reduce the concentrations of haemolytic bacteria in rearing systems.

Pathogenic Bacteria Associated with Different Public Environmental Sites in Mecca City

Background: The hygiene of environmental surfaces from shopping, ATM machines, telephones and computers and miscellaneous sites play role in spreading fecal and total coliform bacteria as well as pathogenic bacteria. Objectives: This study addresses the contaminated common sites by pathogenic or potentially pathogenic bacteria in Mecca, SA. Materials and Methods: A total 648 swab samples were collected and analyzed for presence or absence of pathogenic bacteria. Results: Of the total samples 422 were negative bacterial count (71%) and 226 (29%) were positive. All collected samples (100%) of glass windows in the fish markets were bacterial counted; most dominated was Bacillus spp. (n = 97) and the highest population of species was Enterococcus faecalis (n = 40) and E. coli (n = 16). Conclusion: Some public sites were very contaminated with different types of fecal coliform group of bacteria such as shopping cart handles, inner surfaces and child seats in supermarkets, and the glass windows in the fish market. Acinetobacter haemolyticus and other hemolytic bacteria were isolated from more than site.

Potentially lethal bacteria in leatherback turtle eggs in the wild threaten both turtles and conservationists

The leatherback turtle is an endangered sea turtle whose numbers are in decline. There is a great effort world wide on the part of many conservationists to protect these turtles and their eggs. We previously demonstrated that blood from a leatherback hatchling was infected with a hemolytic acinetobacter bacterium, Acinetobacter sp. HM 746599, implying that the developing embryo may have been infected in the egg. Only about 50% of the eggs laid on a Costa Rican beach hatch due to predation, inundation and within nest factors. This study was conducted to determine whether high bacterial infection rate of eggs incubating in the dark, moist sands of the beach contributes to the low hatching rate. Samples were taken aseptically from adult cloacal fluids and failed and opened eggs in search of potentially lethal bacteria. We identified three bacterial species in selected cloned samples that exhibited hemolytic activity. These bacteria were species of the Bacillus, Pseudomonas and Aeromonas genera. Many of these bacterial species are known pathogens to humans and may account for developmental arrest of the turtle embryo. These bacterial species may also pose a danger to human workers who come in contact with them. Knowledge of the bacteria that can infect and possibly kill leatherback embryos may lead to treatment modalities of leatherback clutches with anti-microbial agents which would allow us to improve the hatching rates of these animals under controlled conditions.

Ornithinibacillus scapharcae sp. nov., isolated from a dead ark clam

A novel Gram-positive, aerobic, motile, hemolytic, endospore-forming and rod-shaped bacterium TW25(T) was isolated from a dead ark clam during a mass mortality event on the South coast of Korea. The strain grew optimally at 30°C, at pH 8-9, and with 1% (w/v) NaCl. The 16S rRNA gene sequence analysis indicated that strain TW25(T) was associated with the genus Ornithinibacillus and that it was most closely related to the type strain of Ornithinibacillus californiensis (98.5% similarity). The dominant cellular fatty acids were iso-C15:0, anteiso-C15:0 and C16:0. The peptidoglycan amino acid type was A4β, containing L: -ornithine and D: -aspartic acid. The polar lipids were diphosphatidylglycerol, phosphatidylglycerol, four unidentified phospholipids, two unidentified aminolipids and two unidentified lipids. The major respiratory quinone was menaquinone-7 (MK-7). The G+C content of genomic DNA was 36.7mol%. DNA-DNA hybridization experiments with related strains revealed lower than 11±3% relatedness. Based on this polyphasic taxonomic study, strain TW25(T) represents a novel species in the genus Ornithinibacillus, for which the name Ornithinibacillus scapharcae sp. nov. is proposed. The type strain is TW25(T) (=KACC 15116(T)=JCM 17314(T)).

Haemorrhagic septicaemia in the hybrid surubim (Pseudoplatystoma corruscans×Pseudoplatystoma fasciatum) caused by Aeromonas hydrophila

Intensive culture of the hybrid surubim (Pseudoplatystoma corruscans × Pseudoplatystoma fasciatum) in Brazil is responsible for the occurrence of diseases and consequent economic losses. However, the causative agents are not well known. The objective of this study was to isolate and to characterize the pathogenic agent responsible for mortalities in cultured surubim and to demonstrate its virulence. Ten fish from a fish farm located in the Mato Grosso do Sul State (Brazil) were collected and 14 haemolytic bacteria characterized as Aeromonas hydrophila were isolated from the kidneys (eight) and brain (six). As an experimental challenge, fish weighing 98.1±23.6 g were injected with 1 mL of saline solution and 2 × 102, 2 × 104, 2 × 106 and 2 × 108 CFU A. hydrophila mL−1. Fish infected with 2 × 108 CFU showed increased external and internal symptoms and mortality of 50±12.5% after 96 h. Increased A. hydrophila concentration was responsible for a decrease in haematocrit percentage and erythrocyte number, lymphocytes and eosinophils, as well as an increase in monocytes, neutrophils, serum agglutination titre and serum antimicrobial activity. It was concluded that A. hydrophila was responsible for characteristic symptoms of bacterial haemorrhagic septicaemia as well as important haematological and immunological alterations, which led to surubim mortality.

Preparation of the Blood-Enriched Agar with the Use of Red Cell Suspension

A culture medium is said to support the growth and development of different microorganisms. Certain bacteria like Staphylococcus aureus and Staphylococcus epidermidis entail hemoglobin found in the red blood cells. Because of its cost effectiveness and availability, expired human blood is being utilized in some developing countries. Despite the widely accepted disadvantages of using human blood as enrichment agent, many laboratories still opt to use it due to the unavailability of sheep blood or due to budgetary reasons. This study determined if the washed expired human blood can be used as an alternative enrichment agent in the preparation of Blood Agar Plate (BAP) culture medium in the isolation of Staphylococcus aureus ATCC 25923 and Staphylococcus epidermidis ATCC 12228. The cultural characteristics and hemolytic reactions of the selected microorganisms were recorded, assessed and compared with their growth in BAP. The stability of the washed expired human blood was evaluated in terms of temperature and storage period. Results reveal that expired human blood with washing improved the morphologic and hemolytic pattern of Staphylococcus aureus. The washing of blood had no effect on Staphylococcus epidermidis because it is a gamma hemolytic bacterium. Both unwashed expired and fresh human blood produced gamma hemolysis due to the interferences still present in them. Both washed expired human blood and washed fresh human blood produced beta hemolysis. Washed expired human blood could be stored for seven days and still could be used for microbial culture. Keywords - Blood, Blood Enriched Agar, Red Cell Suspension

Investigation of presence of α haemolytic streptococci, enterococci and streptococci-like bacteria in different materials originating from pigs

The aim of this investigation was to establish the presence and prevalence of streptococci, enterococci and streptococci-like bacteria in various materials originating from healthy, slaughtered and dead pigs belonging to different categories from several farms and slaughterhouses in the Republic of Serbia. The total number of investigated samples comprised 226 swabs of tonsils and noses from clinically healthy breeders, swabs of tonsils from piglets 5-20 days old, parts of nasopharyngeal tonsils from breeders slaughtered in a slaughterhouse, parts of nasopharyngeal tonsils from piglets slaughtered in a slaughterhouse, swabs of slaughtered pig carcasses from a slaughterhouse, swabs from knives for evisceration in a slaughterhouse, as well as swabs of lungs, abdominal cavity and organs from piglets which died suddenly. The standard microbiological methods were used for investigations of the presence of the listed microorganisms. Commercial biochemical tests were used for the identification of the isolated bacteria and specific sera for capsular antigenes were used for serological determination of the isolated S. suis strains. It was established that the great majority of the isolated strains belonged to the genus Streptococcus (36) (75%), and the minority of the strains belonged to the following genera: Enterococcus (6) (10.4%), Aerococcus (3) (6.2%), Lactococcus (2) (4.2%) and Globicatella (2) (4.2%). The great majority of Streptococcus species belonged to S. suis. The presence of other ? haemolytic streptococci was established in the swabs of nasopharyngeal tonsils: Streptococcus sanguinis (13.8%), Streptococcus salivarius (5.6%), Streptococcus mitis (5.6%), Streptococcus parasanguinis (2.7%) and Streptococcus oralis (2.7%). Also, S. bovis was isolated in a smaller percentage (5.6%). The greatest number of isolated bacteria from the genus Enterococcus belonged to Enterococcus faecalis (80%), while the minority of isolated strains belonged to Enterococcus faecium (20%). The following from the streptococci-like bacteria were isolated: Aerococcus viridans, Globicatella sanguinis and Lactococcus lactis ssp.cremoris.

Tetracycline-resistant bacteria as indicators of antimicrobial resistance in protected waters—The example of the Drwęca River Nature Reserve (Poland)

The objective of this study was to determine the suitability of Tet R tetracycline-resistant bacteria as potential indicators of drug resistance, a parameter of the microbiological quality of river waters in natural reserves which are threatened by man-made pollution. The microbiological assays covered a 15-km long section of the upper reach of the Drwęca River (Poland), a part of the European Ecological “Natura 2000” Network of nature protected areas. The quality of the investigated ecosystem was affected by surface runoffs from the river's agricultural catchment as well as outflows from three fish farms. The counts of Tet R bacteria, incubated at 14 °C and 28 °C on TSA medium with sheep blood and tetracycline, were determined in river water samples. The highest counts of both bacterial groups were determined in samples collected from sites behind fish farms. A statistical analysis of the abundance of Tet R14 °C and Tet R28 °C bacteria revealed significant differences in the size of Tet R28 °C populations at the studied sampling sites ( p = 0.0011), which is why hemolytic bacteria of this group (HemTet R28 °C) were selected for further investigations. The predominant strains in the group of 86 HemTet R28 °C isolates obtained by 16S rRNA gene sequencing were Pseudomonas fluorescens (42 isolates) and Aeromonas hydrophila (28 isolates). Analyses of the identified HemTet R28 °C strains demonstrated MIC ≥256 μg/ml in more than 50% isolates. The MAR index of HemTet R28 °C was in the range of 0.67 at the control site to 1 at sites behind fish farms. The results suggest that tetracycline-resistant bacteria, in particular HemTet R28 °C, are a reliable indicator of antimicrobial resistance and the microbial quality of surface waters polluted due to human activity. The above can be attributed to several factors: (I) the highest percentage share of HemTet R28 °C among HPC28 °C was noted at sites behind fish farms, (II) tetracycline-resistant bacteria quickly respond to environmental changes, as demonstrated by the high level of resistance to tetracycline and a very high MAR index, and (III) genera/species that are easy to culture under laboratory conditions dominate in the qualitative and quantitative composition of the studied bacteria.

Selective toxicity of antimicrobial peptide S-thanatin on bacteria

S-thanatin, an analog of thanatin, was synthesized by substituting the 15th amino acid of threonine with serine, which showed a broad antimicrobial activity against bacteria. We reported earlier that membrane phospholipid was found to be the target for S-thanatin with different mechanism from other antimicrobial peptides. In this study, we have performed its structural characterization by circular dichroism (CD) spectroscopy. The CD analysis showed that S-thanatin retained its overall conformation β-sheet in aqueous buffer, β-turn in 50% trifluoroethanol (TFE) and β-hairpin in 0.4 mM POPC-LUVs. In hemolysis assay, S-thanatin exhibited low hemolytic activity and bacteria selectivity. We investigated the effect of the presence of 33 mol percent cholesterol on the interactions of the antimicrobial peptide S-thanatin with phosphatidylcholine (PC) model membrane systems. The results showed that S-thanatin was more potent at disrupting cholesterol-free bacterial than cholesterol-containing eukaryotic membranes. Thus, in all respects, fluorescence dye leakage experiments indicated that cholesterol inhibited the S-thanatin-induced permeabilization of PC vesicles. Finally, flow cytometry was used to monitor changes in bacterial cell membrane potential and cell membrane integrity, with specific fluorescent dyes DiBAC 4(3) and PI. Adding the respiratory poison CCCP seemed to prevent peptide-induced membrane damage, which suggested that S-thanatin acted at the metabolic level on respiratory chain. These findings might explain why S-thanatin was selective toxicity towards bacteria, but low toxicity towards erythrocytes. It might be due to three factors at least: electrostatic interaction (namely anionic phospholipids); cholesterol; respiratory chain.

Germination and Characterization of Bacillus anthracis and Bacillus cereus in Nematodes

Bacillus anthracis is a Gram‐positive, spore‐forming, rod‐shaped bacterium known to cause anthrax. B. cereus is a related soil dwelling, beta hemolytic bacterium that can cause two food poisoning syndromes characterized by nausea and vomiting. Both species are typically present in soil as spores, yet they do not germinate in soil. We hypothesize that B. cereus and B. anthracis spores germinate in the gut of nematodes. Synchronized cultures of C. elegans were used to determine the effect of B. anthracis and B. cereus on the lifespan of nematodes: these results were inconclusive. Next, co‐plating of C. elegans with: 1) B. anthracis and B. cereus; 2) B. cereus and E. coli; and 3) B. anthracis and E. coli showed no preference as food sorces for C. elegans. B. anthracis spore germination was monitored in real time by co‐plating C. elegans with a B. anthracis strain containing the Pps12 plasmid. Insertion of this plasmid was expected to facilitate the fluorescence of B. anthracis in the gut of C. elegans upon germination. B. anthracis spores fluoresced in germination buffer supplemented with inosine and alanine; however, florescence was not detectable when ingested by C. elegans. Understanding the mechanism of B. anthracis and B. cereus germination is fundamental to preventing infection by each organism. Supported by NIH R25GM063775

Effects of Environmental Parameters on Bacterial Levels in Seawater from Juvenile Green Turtle (Chelonia mydas) kept in Captivity

Bacterial infection is a major cause of high mortality in juvenile sea turtles at the Sea Turtle Conservation Centre, Chonburi Province, Thailand. The attempt is to identify sources of bacterial accumulation and contamination in order to reduce the number of infections. The aim of this study was to determine the effects of live rocks and captivity parameters on microbiological water quality. Microbiological results indicated that the presence of live rocks in juvenile green turtle containers resulted in a reduction of haemolytic bacteria in seawater. Additionally, the high stock density of animals in the captivity has influence on the increased bacterial levels in the water, while temperature of the water was found to have an influence on bacterial growth. The results of this study implied that the environments of captivity have great impact on the bacterial levels in the water, which should be considered for the management of sea turtles as well as other aquatic animals

Detection of hemolytic bacteria from Palythoa caribaeorum (Cnidaria, Zoantharia) using a novel palytoxin-screening assay

Palytoxin (PTX), one of the most potent and chemically complex marine toxins, is predominantly found in zoanthid corals and sporadically in dinoflagellates. Its biosynthesis and metabolic pathways are largely unknown. However, the widespread occurrence of the toxin in phylogenetically distinct marine organisms is consistent with its production by microorganisms and subsequent accumulation in the food chain. To investigate a possible microbial origin, bacteria from two zoanthid corals (Palythoa caribaeorum, Zoanthus pulchellus) and one sponge (Neofibularia nolitangere) were isolated. More than 250 bacteria were screened for hemolysis using a newly developed PTX-screening assay of which 7% showed PTX-like hemolytic activity. 16S rRNA gene sequencing revealed that these bacterial isolates belonged to strains of Bacillus cereus group (n = 11) as well as the genera Brevibacterium (n = 4) and Acinetobacter (n = 2). The results indicate the presence of Na+/K+-ATPase toxins and possibly PTX in hemolytic bacteria from P. caribaeorum.

Determination of emitted airborne microorganisms from a BIO-PAK wastewater treatment plant

Results of a study conducted to assess the degree of airborne microbial contamination generated by a wastewater treatment plant (WWTP) with bioreactor “BIO-PAK” closed treatment system and evaluation of the dispersion of potential pathogens are described. Over the year aerosol samples were collected simultaneously with sedimentation and impact methods from several plant sites and the surroundings. External upwind sites were used as control. Total colony-forming counts of heterotrophic psychrophilic, psychrotrophic, mesophilic, haemolytic bacteria, as well as members of the Enterobacteriaceae family, Staphylococcus, Enterococcus and Pseudomonas genera, actinomycetes and fungi (moulds, yeasts and yeast-like fungi) were determined. Their highest concentrations ranged up to 10 1–10 3 CFU/m 3 (with the exception of moulds exceeding 2 × 10 4) were determined in air sampled inside the bioreactor, its vicinity, and near the grate chamber. Higher species diversity of the family Enterobacteriaceae (including Shigella spp., Yersinia enterocolitica, Escherichia coli, Klebsiella pneumoniae ozaenae) in the air sampled inside or near the bioreactor may imply a health risk for staff exposed for longer periods of time. Notwithstanding, no increased emission of the analysed groups of microorganisms, including faecal bacteria, were found outside the WWTP.

α-Hemolysin from Escherichia coli uses endogenous amplification through P2X receptor activation to induce hemolysis

Escherichia coli is the dominant facultative bacterium in the normal intestinal flora. E. coli is, however, also responsible for the majority of serious extraintestinal infections. There are distinct serotypical differences between facultative and invasive E. coli strains. Invasive strains frequently produce virulence factors such as alpha-hemolysin (HlyA), which causes hemolysis by forming pores in the erythrocyte membrane. The present study reveals that this pore formation triggers purinergic receptor activation to mediate the full hemolytic action. Non-selective ATP-receptor (P2) antagonists (PPADS, suramin) and ATP scavengers (apyrase, hexokinase) concentration dependently inhibited HlyA-induced lysis of equine, murine, and human erythrocytes. The pattern of responsiveness to more selective P2-antagonists implies that both P2X(1) and P2X(7) receptors are involved in HlyA-induced hemolysis in all three species. In addition, our results also propose a role for the pore protein pannexin1 in HlyA-induced hemolysis, as non-selective inhibitors of this channel significantly reduced hemolysis in the three species. In conclusion, activation of P2X receptors and possibly also pannexins augment hemolysis induced by the bacterial toxin, HlyA. These findings potentially have clinical perspectives as P2 antagonists may ameliorate symptoms during sepsis with hemolytic bacteria.

Performance and diarrhoea in piglets following weaning at seven weeks of age: Challenge with E. coli O 149 and effect of dietary factors

Four dietary factors ( ad libitum versus feed restriction, control versus protein restriction at ad libitum feeding, control versus inclusion of lupin as a protein source at ad libitum feeding, and control versus extra vitamin E at ad libitum feeding) were tested in four separate experiments for the effect on diarrhoea. To introduce a diarrhoea-like condition, half of the piglets were challenged with an E. coli O 149 dose of 1 × 10 8 colony forming units on days one and two after weaning (day of weaning = day zero). All piglets were susceptible since the dams were tested mono-zygotic susceptible to the attachment site of E. coli O 149 in the intestines. Each of the four experiments included 32 piglets from 4 sows. The design was a 2 × 2 factorial with dietary factor and E. coli O 149 challenge as the two factors, each at two levels. The piglets were housed individually during the experiment which lasted for 10 days from weaning at 7 weeks of age. The daily recordings included feed intake, weight and faecal score (from 1 = solid and cloddy to 6 = watery and yellow). Faeces from days 1 to 4 were tested for E. coli strains. In addition, blood was sampled and serum was analysed for antibodies to E. coli, IgG and IgM. Generally the E. coli challenge had no effect on growth and feed intake whereas faecal score and number of faecal haemolytic bacteria increased and faecal dry matter decreased. Feed restriction decreased the weight gain while faecal characteristics were unaffected. An analysis including all four experiments revealed that a feed intake of less than 200 g during the first day after weaning seems to be associated with a relatively high incidence of a post-weaning diarrhoea-like condition. Protein restriction decreased faecal score and increased faecal dry matter while weight gain tended to decrease. Inclusion of lupin affected neither weight gain nor faecal characteristics. Extra vitamin E did not affect weight gain while faecal dry matter decreased, and faecal score and number of faecal haemolytic bacteria increased. The dietary treatments had no effect on the measured immunoglobulins. In conclusion, the studied dietary factors could not alleviate a diarrhoea-like condition and at the same time maintain the growth rate. Furthermore, the results indicate that performance can be improved if piglets achieve a daily feed intake of at least 200 g during the first day after weaning.

Functional and quality characteristics of the red blood cell fraction from biopreserved porcine blood as influenced by high pressure processing

The effects of high hydrostatic pressure (HHP) processing, at 400MPa for 15min at 20°C, on the microbiological and functional characteristics of the red blood cell (RBC) fraction obtained from porcine blood, previously preserved by means of lactic acid bacteria (LAB) was studied. Biopreservation was achieved by incubation of inulin-enriched blood inoculated with a LAB strain (Enterococcus raffinosus PS99) for 72h at 5°C. Results showed that incubation of blood with added E. raffinosus followed by HHP treatment reduced the levels of contaminant coliforms, proteolytic, hemolytic bacteria, and Pseudomonas spp. on RCB. Color parameters, protein solubility, foaming and emulsifying properties, as well as texture and water holding capacity of heat-induced gels from RBC were not seriously damaged by the combined treatments. This is a new approach to process and preserve animal blood fractions for the development of functional and/or nutritional food ingredients with added value.

Assessing the potential of Streptococcus pyogenes and Staphylococcus aureus transfer to foods and customers via a survey of hands, hand‐contact surfaces and food‐contact surfaces at foodservice facilities

Abstract Streptococcus pyogenes is an important cause of throat infection that may be transmitted by food. Staphylococcus aureus is a major cause of food intoxication. Both organisms can be transferred to foods or food‐contact surfaces via food handlers. Because both S. pyogenes and S. aureus are hemolytic, the potential for their transfer in a foodservice setting could be assessed by sampling hands, hand‐contact surfaces and food‐contact surfaces for hemolytic bacteria. We performed such a survey at four foodservice facilities from December 2005 to March 2006. Of the 189 total samples, hands (50%), cart handle (40%), pan bottom (38%), door handle (25%) and utensil wrapper (25%) were most often contaminated with hemolytic bacteria. Hand‐contact surfaces were more often contaminated than food‐contact surfaces. S. pyogenes was not isolated but the potential pathogen Streptococcus agalacticae was isolated from one door handle. S. aureus was isolated from a cart handle sampled during the same shift.

Effectiveness of high pressure processing on the hygienic and technological quality of porcine plasma from biopreserved blood

The effects of a high hydrostatic pressure (HHP) treatment (450 MPa, 15 min at 20 °C) on both the microbiological quality and the functional properties of plasma from biopreserved porcine blood were evaluated. Blood was inoculated with Enterococcus raffinosus-PS99 (10 7 ufc mL −1) and stored at 5 °C. After 72-h storage, bacterial counts in inoculated samples decreased by 52, 70, 81 and more than 99% for coliforms, Pseudomonas spp, hemolytic and proteolytic bacteria, respectively. Counts of these bacterial groups were undetectable in the final product after pressurization, whereas total lactic acid bacteria were detected at levels up to 10 2 ufc mL −1. Gelling, foaming and emulsifying properties of the plasma proteins were not noticeably affected by HHP. The results show that it is possible to obtain high-quality and microbiologically stable blood derivatives as functional ingredients, by combining biopreservation and HHP.