329 research outputs found

    Cryopreservation of Salmonella enterica in porcine fecal samples

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    Fecal samples are normally tested for Salmonella soon after collection because storage at any temperature, including refrigeration or freezing, can reduce detection. To evaluate several cryopreservation techniques, autoclaved porcine feces with and without additives were inoculated with 103 CFU S. Derby (UW -9)/g with autoclaved feces pnor to freezing. The mixtures and % of the CFU inoculum that was recovered was as follows: Feces only, 11 %; 50% feces plus 50% glycerol, 45%, 25% feces, 50% glycerol, 25% tetrathionate broth, 63%, 25% feces, 50% glycerol, 25% buffered peptone water (BPW), 66%; 50% feces, 50% glycyceroi/Tris buffer, 58%; 50 % feces, 50% BPW, 30%. When fresh (not autoclaved) feces were used, inoculated with a nalidixic acid resistant S Typhimurium (WI-73), 4% of the inoculum was recovered from undiluted frozen feces wh1le the add1tlon of 50% BPW before freezmg mcreased recovery to 27%

    Risk factors for the detection of Salmonella in ileocolic lymph nodes in US slaughtered pigs.

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    Salmonella harborage at slaughter can be viewed as a nsk for human health through contammation of the pork food cham. Better understanding of herd level factors associated with this harborage would be useful to prioritize further study of epidemiology and control of Salmonella in pork production. Ileocolic lymph node samples collected at slaughter from 115 Midwest US sw1ne herds were assayed for Salmonella entenca. A subset of these herds was collected sequentially one or two additional times. Herd characteristics and management factors were assessed by a written survey. Risk factors were screened at the univariate level (p \u3c 0.3), then offered for Inclusion by stepw1se analysis including herd I sample as a random statistical effect. Pigs at increased risk of Salmonella harborage at slaughter included those placed in finisher barns at heaver weights (OR 1.2 per 10 kg Increased we1ght), those from larger herds (OR 2 0 comparing upper quintile to lower quintile of herd size), those from herds that allowed VISitors w1th recent (\u3c8 h) contact with other herds (OR 2.2), or those fed pelleted feeds (OR 2.1 ). Further invest1gat1on of these risk factors and potential biological mechanisms will requ1re further study

    Repeated observations on the Salmonella culture status of midwest U.S. herds

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    Mesenteric lymph nodes were collected from pigs from 115 Midwest U.S. swine herds at slaughter on two occasions separated by 6-9 months. These herds were sampled up to three additional times during a three-year period, with 30 herds sampled five times. Thirty pigs were sampled at each collection. Herds were categorized positive if one or more samples revealed Salmonella spp. While culture status at collection one was associated with the second sampling collection (p \u3c 0.01), the association was only moderate in strength (OR = 2.6). Herds with three consecutive positive tests (9 of 38) were all positive on sample four. Prevalence estimates were weakly or not correlated between samplings. In conclusion, Salmonella culture status of these swine herds was weakly predictive of future culture results. Accurate description of Salmonella status based on bacterial culture appears to require repeated or ongoing testing

    An estimate of Salmonella prevalence on Illinois swine farms using mesenteric lymph node cultures

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    Accurate description of Salmonella prevalence is an important step toward understanding the epidemiology of the organism. A U.S. national prevalence estimate of fecal prevalence of Salmonella species showed that the organisms were commonly detected on farms. with 58 of 160 farms (38.2%) with one or more positive sample. The same survey, however, suggested that the prevalence rate differed by geographic region, with the southeastern area of the country having more than double the prevalence of the Midwest

    IgG4 inhibits peanut-induced basophil and mast cell activation in peanut-tolerant children sensitized to peanut major allergens

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    BackgroundMost children with detectable peanut-specific IgE (P-sIgE) are not allergic to peanut. We addressed 2 non–mutually exclusive hypotheses for the discrepancy between allergy and sensitization: (1) differences in P-sIgE levels between children with peanut allergy (PA) and peanut-sensitized but tolerant (PS) children and (2) the presence of an IgE inhibitor, such as peanut-specific IgG4 (P-sIgG4), in PS patients.MethodsTwo hundred twenty-eight children (108 patients with PA, 77 PS patients, and 43 nonsensitized nonallergic subjects) were studied. Levels of specific IgE and IgG4 to peanut and its components were determined. IgE-stripped basophils or a mast cell line were used in passive sensitization activation and inhibition assays. Plasma of PS subjects and patients submitted to peanut oral immunotherapy (POIT) were depleted of IgG4 and retested in inhibition assays.ResultsBasophils and mast cells sensitized with plasma from patients with PA but not PS patients showed dose-dependent activation in response to peanut. Levels of sIgE to peanut and its components could only partially explain differences in clinical reactivity between patients with PA and PS patients. P-sIgG4 levels (P = .023) and P-sIgG4/P-sIgE (P < .001), Ara h 1–sIgG4/Ara h 1–sIgE (P = .050), Ara h 2–sIgG4/Ara h 2–sIgE (P = .004), and Ara h 3–sIgG4/Ara h 3–sIgE (P = .016) ratios were greater in PS children compared with those in children with PA. Peanut-induced activation was inhibited in the presence of plasma from PS children with detectable P-sIgG4 levels and POIT but not from nonsensitized nonallergic children. Depletion of IgG4 from plasma of children with PS (and POIT) sensitized to Ara h 1 to Ara h 3 partially restored peanut-induced mast cell activation (P = .007).ConclusionsDifferences in sIgE levels and allergen specificity could not justify the clinical phenotype in all children with PA and PS children. Blocking IgG4 antibodies provide an additional explanation for the absence of clinical reactivity in PS patients sensitized to major peanut allergens

    Salmonella prevalence in market weight pigs before and after shipment to slaughter

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    Samples commonly used for microbiological culture of subclinical Salmonella infection in market weight pigs include fecal material, mesenteric lymph nodes, cecal contents, rectal contents, and rectal swabs. In epidemiologic investigations, collection of abanoir samples offers certain advantages over farm collected samples. Sampling at slaughter offers the advantage of a wider range of sample types. For practical reasons, samples collected on the farm for microbiological culture are usually limited to fecal samples, whereas slaughter samples can include lymph node and higher gut contents. The ease of collection at the slaughter plant facilitates sampling a large number of herds. Detection of Salmonella in slaughtered pigs is also a useful indicator of risk to pork safety, because slaughter processing is the primary point where direct risk of entry into the food chain exists. However, it is possible that pigs may become infected during transportation and lairage. Further, it is possible that pigs harbor Salmonella while on the farm, but they do not shed the organism into feces. The stress of events iromediately pre-slaughter may then induce these non-shedding infected pigs to begin shedding

    Aneurysms—from traumatology to screening

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    This paper deals with aneurysmal disease, primarily when localized in the abdominal aorta. It is based on the Olof Rudbeck lecture 2009. Aneurysm is a localized widening of an artery, and its definition has become an important issue today when the disease is in focus for screening programmes. Aetiology and pathogenesis are still poorly understood, but a genetic component determining the strength of the aortic wall is important, and there is a strong male dominance. Historically, several attempts have been made to treat the disease, but reconstructive treatment has been possible only since 1951, in an increasing number of cases performed endovascularly. By early detection through screening, and thereby the possibility to treat before rupture, it has now become possible to decrease the total mortality from the disease in the population

    Direct and indirect transmission of four Salmonella enterica serotypes in pigs

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    <p>Abstract</p> <p>Background</p> <p>Feed-borne spread of <it>Salmonella </it>spp. to pigs has been documented several times in recent years in Sweden. Experiences from the field suggest that feed-associated serotypes might be less transmittable and subsequently easier to eradicate from pig herds than other serotypes more commonly associated to pigs. Four <it>Salmonella </it>serotypes were selected for experimental studies in pigs in order to study transmissibility and compare possible differences between feed-assoociated (<it>S </it>Cubana and <it>S </it>Yoruba) and pig-associated serotypes (<it>S </it>Derby and <it>S </it>Typhimurium).</p> <p>Methods</p> <p>Direct contact transmission was studied in four groups of pigs formed by six 10-week-old salmonella negative pigs commingled with two fatteners excreting one of the four salmonella serotypes. Indirect transmission was studied by putting six 10-week-old salmonella negative pigs in each of four salmonella contaminated rooms. Each room had previously housed a group of pigs, excreting one of the four selected serotypes.</p> <p>All pigs were monitored for two weeks with respect to the faecal excretion of salmonella and the presence of serum antibodies. At the end of the trial, eight samples from inner tissues and organs were collected from each pig at necropsy.</p> <p>Results</p> <p>In the four direct transmission groups, one pig shed <it>Salmonella </it>(Cubana) at one occasion. At necropsy, <it>S </it>Typhimurium was isolated from one pig.</p> <p>In the indirect transmission groups, two pigs in the Yoruba room and one pig in each of the other rooms were excreting detectable levels of <it>Salmonella </it>once during the study period of two weeks. At necropsy, <it>S </it>Derby was isolated from one of six pigs in the Derby room and <it>S </it>Typhimurium was isolated from four of the six pigs in the Typhimurium room.</p> <p>No significant serological response could be detected in any of the 48 pigs.</p> <p>Conclusions</p> <p>These results show that all four selected serotypes were able to be transmitted in at least one of these field-like trials, but the transmission rate was low in all groups and no obvious differences between feed-associated and pig-associated serotypes in the transmission to naïve pigs and their subsequent faecal shedding were revealed. However, the post mortem results indicated a higher detection of <it>S </it>Typhimurium in the ileocecal lymph nodes of pigs introduced into a contaminated environment in comparison with the other three serotypes.</p

    Lung adenocarcinoma originates from retrovirus infection of proliferating type 2 pneumocytes during pulmonary post-natal development or tissue repair

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    Jaagsiekte sheep retrovirus (JSRV) is a unique oncogenic virus with distinctive biological properties. JSRV is the only virus causing a naturally occurring lung cancer (ovine pulmonary adenocarcinoma, OPA) and possessing a major structural protein that functions as a dominant oncoprotein. Lung cancer is the major cause of death among cancer patients. OPA can be an extremely useful animal model in order to identify the cells originating lung adenocarcinoma and to study the early events of pulmonary carcinogenesis. In this study, we demonstrated that lung adenocarcinoma in sheep originates from infection and transformation of proliferating type 2 pneumocytes (termed here lung alveolar proliferating cells, LAPCs). We excluded that OPA originates from a bronchioalveolar stem cell, or from mature post-mitotic type 2 pneumocytes or from either proliferating or non-proliferating Clara cells. We show that young animals possess abundant LAPCs and are highly susceptible to JSRV infection and transformation. On the contrary, healthy adult sheep, which are normally resistant to experimental OPA induction, exhibit a relatively low number of LAPCs and are resistant to JSRV infection of the respiratory epithelium. Importantly, induction of lung injury increased dramatically the number of LAPCs in adult sheep and rendered these animals fully susceptible to JSRV infection and transformation. Furthermore, we show that JSRV preferentially infects actively dividing cell in vitro. Overall, our study provides unique insights into pulmonary biology and carcinogenesis and suggests that JSRV and its host have reached an evolutionary equilibrium in which productive infection (and transformation) can occur only in cells that are scarce for most of the lifespan of the sheep. Our data also indicate that, at least in this model, inflammation can predispose to retroviral infection and cancer
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