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Listeria monocytogenes infections in Canada.

https://arctichealth.org/en/permalink/ahliterature241209
Source
Clin Invest Med. 1984;7(4):315-20
Publication Type
Article
Date
1984
Author
J W Davies
E P Ewan
P. Varughese
S E Acres
Source
Clin Invest Med. 1984;7(4):315-20
Date
1984
Language
English
Publication Type
Article
Keywords
Adolescent
Adult
Animals
Canada
Child
Child, Preschool
Disease Reservoirs
Hospitalization
Humans
Infant
Infant, Newborn
Listeria monocytogenes - classification
Listeriosis - congenital - epidemiology - mortality - veterinary
Middle Aged
Serotyping
Abstract
Since its first isolation by Murray in 1926 Listeria monocytogenes has become recognized as a significant pathogen occurring worldwide and involving a wide range of wild and domestic animals including man. The first confirmed human listeriosis case in Canada was published by Stoot in 1951. A later survey based on records maintained at the Laboratory Centre for Disease Control, Ottawa showed 101 cases detected over a 21 year period in nine provinces. The overall mortality was 30%. The most frequently isolated serotype was 4b followed by 1 and 1b. Prior to the Nova Scotia epidemic (41 cases) of 1981, fewer than 15 cases per annum had been diagnosed based on hospital discharge records. The Nova Scotia epidemic was unique in that the source and mode of transmission of the organism were determined. Sixty-three strains isolated from this outbreak were typed, and with the exception of one 1a strain, were identified as 4b. These were subsequently classified mainly as phage type 00 042 0000 and 00 002 0000. Listeriosis appears to be a common infection in the animal population in Canada primarily in cattle, sheep, chinchillas, chickens and goats. Outbreaks have been described in rabbits, goats, and chinchillas. Chinchilla farms were affected in one outbreak (serotype 1) in Nova Scotia which was attributed to feeding a new batch of meal containing beet pulp. Many aspects of the epidemiology of listeriosis are obscure. A cycle involving contaminated soil and consumption of raw vegetables has been confirmed as the cause of the Nova Scotia epidemic and could explain a proportion of the sporadic cases.(ABSTRACT TRUNCATED AT 250 WORDS)
PubMed ID
6442654 View in PubMed
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Listeria monocytogenes isolates from invasive infections: variation of sero- and genotypes during an 11-year period in Finland.

https://arctichealth.org/en/permalink/ahliterature185899
Source
J Clin Microbiol. 2003 Apr;41(4):1694-700
Publication Type
Article
Date
Apr-2003
Author
Susanna Lukinmaa
Maria Miettinen
Ulla-Maija Nakari
Hannu Korkeala
Anja Siitonen
Author Affiliation
Laboratory of Enteric Pathogens, National Public Health Institute, FIN-00300 Helsinki, Finland.
Source
J Clin Microbiol. 2003 Apr;41(4):1694-700
Date
Apr-2003
Language
English
Publication Type
Article
Keywords
Adolescent
Adult
Aged
Aged, 80 and over
Bacterial Typing Techniques
Child
Child, Preschool
Electrophoresis, Gel, Pulsed-Field
Female
Finland - epidemiology
Genetic Variation
Genotype
Humans
Infant
Infant, Newborn
Listeria monocytogenes - classification - genetics
Listeriosis - epidemiology - microbiology
Male
Middle Aged
Serotyping
Abstract
Listeria monocytogenes strains that were isolated from 314 human listeriosis cases in Finland during an 11-year period were analyzed by O:H serotyping and pulsed-field gel electrophoresis (PFGE). Serotyping divided the isolates into five serotypes, the most common being 1/2a (53%) and 4b (27%). During the study period, the number of cases caused by serotype 1/2a increased from 22% in 1990 to 67% in 2001, and those caused by serotype 4b decreased from 61 to 27%, respectively. PFGE with restriction enzyme AscI divided the strains into 81 PFGE genotypes; among strains of serotypes 1/2a and 4b, 49 and 18 PFGE types were seen, respectively. PFGE type 1 (serotype 1/2a) was the most prevalent single type (37 strains). Together with six other, closely related PFGE types, PFGE type 1 formed a group of 71 strains, representing 23% of all 314 strains. Strains of PFGE type 1 have also been isolated from cold smoked fish, suggesting a source of human infections caused by this type. Moreover, PFGE type 24 (serotype 1/2c) was significantly associated with gender: 5% of 180 male subjects but none of 132 female subjects (P = 0.012). An electronic database library was created from the PFGE profiles to make possible the prompt detection of new emerging profiles and the tracing of potential infection clusters in the future.
Notes
Cites: J Clin Microbiol. 1994 Dec;32(12):2936-437883880
Cites: Lancet. 1989 Mar 11;1(8637):5492564074
Cites: Clin Infect Dis. 1995 Jan;20(1):66-727727673
Cites: Int J Food Microbiol. 1990 May;10(3-4):255-622118796
Cites: Microbiol Rev. 1991 Sep;55(3):476-5111943998
Cites: JAMA. 1992 Apr 15;267(15):2041-51552639
Cites: Vet Rec. 1993 Aug 14;133(7):165-68236705
Cites: Appl Environ Microbiol. 1994 Jul;60(7):2584-928074531
Cites: J Clin Microbiol. 1995 Sep;33(9):2233-97494007
Cites: Int J Food Microbiol. 1996 Oct;32(3):289-998913801
Cites: Int J Food Microbiol. 1996 Oct;32(3):343-558913805
Cites: Epidemiol Infect. 1996 Dec;117(3):429-368972666
Cites: N Engl J Med. 1997 Jan 9;336(2):100-58988887
Cites: Pediatr Infect Dis J. 1997 Aug;16(8):827-89271054
Cites: J Infect Dis. 1998 Jan;177(1):155-609419182
Cites: Int J Food Microbiol. 1998 Aug 18;43(1-2):61-719761339
Cites: J Microbiol Methods. 1999 Apr;35(3):237-4410333075
Cites: Int J Food Microbiol. 1999 Mar 1;47(1-2):111-910357279
Cites: J Clin Microbiol. 1999 Jul;37(7):2176-8210364582
Cites: J Clin Microbiol. 1999 Jul;37(7):2358-6010364616
Cites: J Infect Dis. 2000 May;181(5):1838-4110823797
Cites: Int J Food Microbiol. 2001 Apr 11;65(1-2):55-6211322701
Cites: Appl Environ Microbiol. 2001 Jun;67(6):2586-9511375167
Cites: Emerg Infect Dis. 2001 May-Jun;7(3):382-911384513
Cites: J Clin Microbiol. 2001 Jul;39(7):2704-711427601
Cites: Emerg Infect Dis. 2001 Nov-Dec;7(6):983-911747725
Cites: Prev Vet Med. 2002 Feb 14;53(1-2):55-6511821137
Cites: Int J Food Microbiol. 2002 Jul 25;77(1-2):83-9012076041
Cites: J Food Prot. 2003 Feb;66(2):249-5512597485
Cites: J Infect Dis. 1978 Jul;138(1):17-2398594
Cites: N Engl J Med. 1983 Jan 27;308(4):203-66401354
Cites: N Engl J Med. 1985 Feb 14;312(7):404-73918263
Cites: JAMA. 1995 Apr 12;273(14):1118-227707600
PubMed ID
12682162 View in PubMed
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Occurrence, Persistence, and Contamination Routes of Listeria monocytogenes Genotypes on Three Finnish Dairy Cattle Farms: a Longitudinal Study.

https://arctichealth.org/en/permalink/ahliterature297944
Source
Appl Environ Microbiol. 2018 02 15; 84(4):
Publication Type
Journal Article
Research Support, Non-U.S. Gov't
Date
02-15-2018
Author
Hanna Castro
Anniina Jaakkonen
Marjaana Hakkinen
Hannu Korkeala
Miia Lindström
Author Affiliation
Department of Food Hygiene and Environmental Health, Faculty of Veterinary Medicine, University of Helsinki, Helsinki, Finland.
Source
Appl Environ Microbiol. 2018 02 15; 84(4):
Date
02-15-2018
Language
English
Publication Type
Journal Article
Research Support, Non-U.S. Gov't
Keywords
Animals
Cattle
DNA, Bacterial - genetics
Dairying
Disease Reservoirs - microbiology - veterinary
Electrophoresis, Gel, Pulsed-Field
Farms
Feces - microbiology
Female
Finland - epidemiology
Genotype
Humans
Listeria monocytogenes - genetics - isolation & purification
Listeriosis - epidemiology - microbiology - veterinary
Longitudinal Studies
Mammary Glands, Animal - microbiology
Milk - microbiology
Abstract
The molecular epidemiology of Listeria monocytogenes was investigated in a longitudinal study of three Finnish dairy farms during 2013 to 2016. A total of 186 bulk tank milk (BTM), 224 milk filter sock (MFS), and 1,702 barn environment samples were analyzed, and isolates of L. monocytogenes were genotyped using pulsed-field gel electrophoresis. L. monocytogenes occurred throughout the year in all sample types, and the prevalence in MFS increased significantly during the indoor season. L. monocytogenes was more prevalent in MFS (29%) than in BTM (13%) samples. However, the prevalence of L. monocytogenes varied more between farms in samples of MFS (13 to 48%) than in BTM (10 to 16%). For each farm, the L. monocytogenes genotypes detected were classified by persistence (defined as persistent if isolated from =3 samples during =6 months) and predominance (defined as predominant if >5% prevalence on at least one farm visit). The prevalence of sporadic genotypes was 4 to 5% on all three farms. In contrast, the prevalence of persistent predominant genotypes varied between farms by 4% to 16%. The highest prevalence of persistent predominant genotypes was observed on the farm with the poorest production hygiene. Persistent predominant genotypes were most prevalent on feeding surfaces, water troughs, and floors. Genotypes isolated from the milking system or from cow udders had a greater relative risk of occurring in BTM and MFS than genotypes that only occurred elsewhere in the farm, supporting the hypothesis that L. monocytogenes is transmitted to milk from contamination on the udder surface or in the milking equipment.IMPORTANCEListeria monocytogenes is a ubiquitous environmental bacterium and the causative agent of a serious foodborne illness, listeriosis. Dairy products are common vehicles of listeriosis, and dairy cattle farms harbor L. monocytogenes genotypes associated with human listeriosis outbreaks. Indeed, dairy cattle farms act as a reservoir of L. monocytogenes, and the organism is frequently detected in bulk tank milk (BTM) and in the feces of clinically healthy cows. The ecology of L. monocytogenes in the farm environment is complex and poorly understood. Isolates of the same L. monocytogenes genotype can occur in the farm for years, but the factors contributing to the persistence of genotypes on dairy farms are unknown. Knowledge of the persistence patterns and contamination routes of L. monocytogenes on dairy farms can improve management of the contamination pressure in the farm environment and aid in the development of focused control strategies to reduce BTM contamination.
PubMed ID
29222098 View in PubMed
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Surveillance of Listeria monocytogenes in human and environmental specimens in Nova Scotia, 1974 to 1981.

https://arctichealth.org/en/permalink/ahliterature241208
Source
Clin Invest Med. 1984;7(4):325-7
Publication Type
Article
Date
1984
Author
J A Embil
E P Ewan
S W MacDonald
Source
Clin Invest Med. 1984;7(4):325-7
Date
1984
Language
English
Publication Type
Article
Keywords
Adult
Animals
Cats
Dogs
Environmental Microbiology
Female
Fetal Blood - microbiology
Food Microbiology
Humans
Infant, Newborn
Listeria monocytogenes - classification
Male
Nova Scotia
Placenta - microbiology
Pregnancy
Rectum - microbiology
Semen - microbiology
Urine - microbiology
Vagina - microbiology
Abstract
We examined specimens for L. monocytogenes using the "cold enrichment" technique of Gray et al. (J. Bacteriol., 55: 471, 1948) and a nalidixic agar plate (Ann. Inst. Pasteur 111: 90, 1966). Between 1974 and May 1981, we isolated L. monocytogenes from four of 5,255 specimens (rectal, vaginal and placental swabs; blood; spinal fluid; semen; necropsy material) which came from eight human populations (neonates, children, adult men, and pregnant and nonpregnant women) and from 161 animals. Three of the isolated strains were type 1, and they came from a newborn born at 32 weeks' gestation, that child's mother, and another woman who had recently delivered. The fourth (type 4b) came from a newborn twin born at 36 1/2 weeks' gestation. In June through October 1981, in 529 specimens, we isolated L. monocytogenes type 1/2 from two of four larvae tested (four earwigs and five slugs were all negative) and from three of 27 samples of fresh chicken liver (however, 18 samples of coleslaw were negative). At the same time, we isolated L. monocytogenes (not yet typed) from a rectal swab from one of 112 dogs examined. Rectal swabs from 107 cats were negative, as were vaginal swabs from 144 women and urine samples from 108 newborns.
PubMed ID
6442655 View in PubMed
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