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Query: UMLS:C0009443 (cold)
 92,137 document(s) hit in 31,850,051 MEDLINE articles (0.00 seconds)

Yersinia enterocolitica biotype 1, serotype O:21 was isolated from feces or rectal washings of three members of one family in northwestern Saskatchewan. The three isolates gave positive pathogenicity tests in guinea pigs with cultures grown at 22 degrees C as inoculum. All three cases showed clinical symptoms consistent with yersiniosis. All three cases had symptoms of diarrhea and abdominal pain, and two cases had recorded fever. In two cases, appendicitis was initially suspect. One case with ileitis and peritonitis was fatal. The environmental source of the infection was not found, but river water, milk, and person-to-person spread are discussed as possible sources of the infections. The need for microbiology laboratories to culture stool specimens specifically for Y. enterocolitica, using cold-enrichment techniques is emphasized. This family outbreak of yersiniosis provides further evidence that certain biotype 1 strains of Y. enterocolitica are pathogenic.
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PMID:Family outbreak of yersiniosis. 715 10

An epizootic of an acutely fatal enteric disease in a colony of squirrel monkeys (Saimiri sciureus) was attributed to infection by Yersinia pseudotuberculosis serotype III. Of a total adult population of 96 animals at risk, there were six fatal cases of yersiniosis. Serological evaluation of the colony just after the outbreak ended revealed that 22 of 60 monkeys tested (37%) had significant antibody to Y. pseudotuberculosis (microagglutination titer of greater than or equal to 1:80) but did not have clinical disease. The outstanding pathological lesions noted in dying monkeys were acute, purulent, necrotic and focal enteritis primarily affecting the jejunum and ileum and focal hepatic necrosis and abscessation. Y. pseudotuberculosis was isolated from the organs of two of the dying monkeys. Using cold enrichment techniques, Yersinia was also isolated from the feces of two apparently healthy monkeys (both seropositive), from the spleen of a monkey dying of other causes, and from the colon contents of a stillborn squirrel monkey baby. All isolates had the same biotype and serotype. An episode of abortions was associated both temporally and spatially with the fatal cases of yersiniosis, and Y. pseudotuberculosis was cultured from the uterus of two of the dying monkeys, suggesting that yersinia infection may be associated with abortion, as well as with enteric infection, in these animals.
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PMID:Yersinia pseudotuberculosis infection: study of an epizootic in squirrel monkeys. 724 Mar 87

Thirty-one tongues from apparently normal, freshly slaughtered pigs were assayed for the presence of Yersinia enterocolitica by different enrichment and postenrichment techniques. Sixteen different isolates were recovered, including six of serotype O:8, four of serotype O:6,30, two of serotype O:3 phage type IXb, and one each of serotypes O:13,7, O:18, and O:46. One isolate was not typable. Cold enrichment in phosphate-buffered saline followed by treatment with dilute KOH or subsequent enrichment in modified Rappaport broth recovered 12 and 7 isolates, respectively. Four of the same isolates were recovered from the same tongues by both procedures. Cold enrichment without a selective postenrichment treatment recovered two isolates. Direct enrichment in modified Rappaport broth or modified selenite broth was ineffective in recovering yersiniae, as no isolates were obtained by either method. All of the serotype O:8 isolates were virulent to mice, causing the death of adults after oral challenge. This is the first report that associates Y. enterocolitica serotype O:8 with a natural reservoir.
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PMID:Isolation of virulent Yersinia enterocolitica from porcine tongues. 733 66

Infections linked in time and space with Yersinia enterocolitica (serovar 0 : 9, biotype 2, lysotype X3) were observed in 6 cases within one university hospital. After a hospital epidemic in Finland in 1973 (involving 7 persons) this is the 2nd such observation. The spread was demonstrated in two areas. The probable source of infection of one patient group (n = 3) was a 48-year-old dialysis patient admitted with a febrile condition without enteritic symptoms. Pathogens could be demonstrated in his faeces by direct culture, in two contact persons cultivation was possible only with cold enrichment. Blood cultures of the first patient were negative. At about the same time 3 further infections with Yersinia enterocolitica of the same characteristics were observed in hospital personnel from different units. Frequent exchange of staff and patients among affected wards increases likelihood of cross-infection. A dialysis nurse with Yersinia arthritis was the possible link between patients and personnel. Transference of infection from one person to another can be assumed in the above cases.
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PMID:[Spread of Yersinia enterocolitica infection within a hospital (author's transl)]. 735 85

The survey of 200 children with diarrhea revealed the presence of enteric yersiniosis in 31 children (15.5%). Y. enterocolitica culture was isolated from the feces of 17 children (8.5%), diagnostic serological shifts were detected in 27 children (13.5%). Among 100 children hospitalized with diarrhea of previously established etiology (dysentery, salmonellosis, etc) 6 children were found to have yersiniosis. The survey of 100 practically healthy children did not reveal any cases of enteric yersiniosis or healthy carriership. To isolate Yersinia, the feces were incubated in phosphate buffer in the cold (4--6 degrees C) and then inoculated into common diagnostic media for enterobacteria. Antibodies were detected in the indirect hemagglutination test with the use of dried erythrocytic yersiniosis diagnostic reagent. A tentative diagnostic titer of 1 : 200 was determined. Antibodies to the causative agent appeared on the 1st week, reached the maximum level on the 2nd and then gradually decreased. The clinical symptoms of the enteric form of yersiniosis resemble those of other kinds of infectious diarrhea, non-dysenteric in etiology. The authors believe that it is necessary for all children with diarrhea, especially at the age of 1--7 years, to be examined for enteric yersiniosis.
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PMID:[Diagnostic value of bacteriologic and serologic studies in detecting intestinal yersiniosis in children]. 744 57

The antibacterial effects of a 3% solution of lactic acid at 55 degrees C were assessed, by examining aerobic bacterial growth on artificially-inoculated pork fat and lean tissue. Discs of fat or lean tissues, each of 10 cm2 surface area, were aseptically excised from pork Longissimus dorsi muscle and inoculated with the cold tolerant pathogens Listeria monocytogenes 4b Scott A no. 3, Yersinia enterocolitica 0:4,32 or Aeromonas hydrophila ATCC 7966, or with the wild type spoilage bacteria Pseudomonas fragi or Brochothrix thermosphacta. After inoculation, each meat disc was immersed in water or lactic acid for 15 s and aerobic bacterial growth followed during 15 days of storage at 4 degrees C. P. fragi and B. thermosphacta grew on both fat and lean, but the pathogens grew on fat tissue only and A. hydrophila did not survive on lean. Lactic acid reduced all test bacteria on fat to below detectable levels within 4 days of treatment and no bacteria could be recovered from acid-treated fat surfaces for the remainder of the 15-day storage interval. Bacteria attached to lean were generally more resistant to lactic acid. In some instances the acid was bacteriostatic (P. fragi, L. monocytogenes) while in others the population declined at a greatly reduced rate as compared with a similar population on fat (B. thermosphacta, Y. enterocolitica). A. hydrophila was equally sensitive to lactic acid on lean and fat. Depending upon the tested strain, tissue type and storage time, maximum reductions in the number of bacteria recovered from acid treated pork ranged from 1 to 8 log cycles. The high bactericidal efficacy of lactic acid applied to pork fat was attributable to a low tissue pH, which varied from 3.49 to 4.41 during the 15 days of aerobic storage.
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PMID:Lactic acid inhibition of the growth of spoilage bacteria and cold tolerant pathogens on pork. 754 45

The effect of a 82 MDa plasmid or its 25 MDa DNA fragment and growth temperature on the qualitative and the quantitative fatty acid and phospholipid composition of Yersinia pseudotuberculosis cells has been examined. In the cold, plasmid-containing and plasmid-free strains failed to differ appreciably in the contents of phospholipid and fatty acid. The exceptions were an elevated proportion of diphosphatidylglycerine and a decreased fatty acid unsaturation index in the plasmidless cells and those harbouring an incomplete 57 MDa plasmid in comparison with the strain containing the 82 MDa plasmid. At 37 degrees C, the lack of the 82 MDa plasmid or its 25 MDa fragment gave rise to a phospholipid of unknown structure, led to a sharp decrease in phospholipid content, in PE amount in particular, with a concurrent increase in the quantities of CL and LPE, and with a reduction in index of fatty acid unsaturation. The 82 MDa plasmid seems to be associated with a cancelling a temperature-dependent regulation of lipid synthesis and as a result, both the 'cold' and the 'warm' variants of the plasmid-containing strain possessed basically the close related lipid contents. Changes in composition of the polar head groups of the membrane phospholipids and in the extent of fatty acid unsaturation were suggested to be connected with an antibiotic hypersensitivity revealed earlier in plasmid-free Y. pseudotuberculosis.
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PMID:Mutual influence of plasmid profile and growth temperature on the lipid composition of Yersinia pseudotuberculosis bacteria. 761 51

Disease control by vaccination is widely used in European salmonid aquaculture against vibriosis (Vibrio anguillarum), cold-water vibriosis (Vibrio salmonicida), yersiniosis or enteric redmouth disease (Yersinia ruckeri) and furunculosis (Aeromonas salmonicida subsp. salmonicida). The vaccines against the Vibrio spp. and Y. ruckeri have proven effective especially when administered by injection. Furunculosis vaccines have been less successful and have relied on combination with potent adjuvants to achieve acceptable protection. Application of modern molecular techniques to furunculosis research has delivered a crop of experimental vaccines that incorporate purified virulence factors and have shown increased protection during challenge. Gene technology has also been used to create a defined, nonreverting mutation in a strain of A. salmonicida, which has enhanced the feasibility of attenuated live vaccines. The development of experimental subunit vaccines against the viral infections and the continued advances in the field of immunostimulants, adjuvants and antigen carriers provide considerable promise for the future development of commercial vaccines for use in salmonid aquaculture.
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PMID:Vaccination in European salmonid aquaculture: a review of practices and prospects. 773 70

Yersinia strains recovered from routine stool cultures (n = 13,534) as well as clinical symptoms in the patients were analysed in order to establish whether enteric Yersinia enterocolitica strains recovered only after cold enrichment cultures shared the same pathogenicity markers and caused the same symptoms as strains from primary cultures. 93% of the 201 Yersinia isolates were Y. enterocolitica strains and 71% of these were of serotype O3. Nearly 40% of all Y. enterocolitica strains and 21% of serotype O3 strains were isolated only after 1 week's cold enrichment of stool specimens. Practically all Y. enterocolitica O3 strains, whether from primary or cold enrichment cultures, were pathogenic not only on the basis of the serotype but also on the basis of Congo-red uptake and calcium-dependent growth at 35 degrees C (CR-MOX test). The symptoms in patients with Y. enterocolitica O3 from primary and cold enrichment cultures were similar except that abdominal pains were more frequent (p < 0.05) in the former. Arthropathia, mesenteric lymphadenitis and erythema nodosum were detected in 15% of the patients with Yersinia isolates and were more frequent in patients with isolates from cold enrichment or without diarrhea.
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PMID:Increased yields of pathogenic Yersinia enterocolitica strains by cold enrichment. 774 91

Dilutions of faecal samples spiked with Yersinia enterocolitica O:3 were analysed using immunomagnetic separation (IMS) followed by PCR. In 10% faecal dilutions with added Y. enterocolitica cells, the limit of detection was 200 cells g-1 faeces. Faecal samples from 38 pigs were analysed by IMS-PCR in parallel with detection and quantification of Y. enterocolitica O:3 using cold pre-enrichment culturing. Of the 15 culture-positive samples, only two were detected with IMS-PCR. These two samples contained 40-400 Y. enterocolitica O:3 cells g-1 faeces; the highest level found in the investigation. This indicated that the low sensitivity of IMS-PCR was due to low amounts of cells in the faecal samples. Swab samples from 195 pig tonsils, taken on a slaughterline were examined using IMS-PCR and culture detection. Of 164 culture-positive samples, 60 were positive with IMS-PCR. In addition, IMS-PCR was positive for three culture-negative samples. Forty-five of the samples were further examined by IMS-PCR after 7-10 d of cold pre-enrichment. All 31 culture-positive samples as well as five culture-negative samples were detected by IMS-PCR. From these data it can be concluded that IMS-PCR can be used to detect Y. enterocolitica O:3 cells after pre-enrichment, but direct detection needs further optimization of the sample preparation procedures.
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PMID:Detection of Yersinia enterocolitica O:3 in faecal samples and tonsil swabs from pigs using IMS and PCR. 775 85


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