Volume 11, Number 12—December 2005
Methicillin-resistant Staphylococcus aureus in Pig Farming
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|EID||Voss A, Loeffen F, Bakker J, Klaassen C, Wulf M. Methicillin-resistant Staphylococcus aureus in Pig Farming. Emerg Infect Dis. 2005;11(12):1965-1966. https://dx.doi.org/10.3201/eid1112.050428|
|AMA||Voss A, Loeffen F, Bakker J, et al. Methicillin-resistant Staphylococcus aureus in Pig Farming. Emerging Infectious Diseases. 2005;11(12):1965-1966. doi:10.3201/eid1112.050428.|
|APA||Voss, A., Loeffen, F., Bakker, J., Klaassen, C., & Wulf, M. (2005). Methicillin-resistant Staphylococcus aureus in Pig Farming. Emerging Infectious Diseases, 11(12), 1965-1966. https://dx.doi.org/10.3201/eid1112.050428.|
We conducted a study among a group of 26 regional pig farmers to determine the methicillin-resistant Staphylococcus aureus prevalence rate and found it was >760 times greater than the rate of patients admitted to Dutch hospitals. While spa-type t108 is apparently a more widespread clone among pig farmers and their environment, we did find other spa-types.
Methicillin-resistant Staphylococcus aureus (MRSA) has become a major nosocomial pathogen, highly prevalent in many European countries and throughout the world (1). In the Netherlands, the prevalence of MRSA among clinical isolates is still <1%, among the lowest in Europe (1). This low prevalence is probably best explained by the national policy that entails strict screening and isolation of all persons who are considered at high risk for MRSA when admitted to a hospital. This high-risk population has essentially consisted of patients admitted to or treated in foreign hospitals. As a result of this policy for all healthcare institutions, the prevalence of MRSA in the Dutch community is extremely low as well. In a recent study among ≈10,000 patients admitted to 4 Dutch hospitals, 23% carried S. aureus, but only 0.03% of the isolates were methicillin-resistant (2).
In July 2004, we unexpectedly found MRSA in the preoperative screening cultures of a 6-month-old girl before thoracic surgery. Neither the girl nor her family (parents, 1 sister) had a history of traveling or admission to a foreign hospital. In the following months, the girl remained colonized with MRSA during consecutive decolonization attempts. Subsequently, the girl's parents were found to be positive for MRSA. The family lived on a farm and raised pigs.
To further investigate pig farming as a possible source of MRSA in Dutch patients, we screened a selection of pigs owned by the MRSA-positive farmer, and other regional pig farmers in November 2004. In January and February 2005, 2 new cases of MRSA were identified, one in a pig farmer from a different region and one in the son of a veterinarian who worked mostly with pigs. Subsequently, the strain was also isolated from the veterinarian and from a nurse in the hospital unit to which the son was admitted.
Although the aforementioned cases were unrelated in time and location, they shared some features. In all the cases, other family members were MRSA-positive, decolonization was repeatedly unsuccessful, and genotyping performed in the National Institute of Public Health and Environment (RIVM, Bilthoven, the Netherlands) showed the strains were not typeable by pulsed-field gel electrophoresis (PFGE) with restriction endonuclease SmaI (the standard method).
Initially, the nares of 10 pigs were cultured. All were negative for MRSA. At a later stage, the perineum of 30 pigs was cultured; 1 was positive for MRSA. The regional pig farmers were screened (throat and nares) during a monthly professional meeting that happened to be on the farm of the MRSA-positive family, at the time of investigation. With the exception of this meeting, the farmers had no further epidemiologic links, other than being from the southeastern region of the Netherlands. Six (23%) of the 26 farmers were colonized with MRSA.
As mentioned above, all MRSA isolates were resistant to digestion with restriction-endonuclease SmaI, when typing with PFGE was attempted. To ensure that we did not falsely classify a pig-related staphylococcal species as MRSA, the identification of all isolates was confirmed by testing for the presence of a S. aureus–specific DNA element as well as the MecA gene, according to the methods of Reischl et al. (3). To compare the MRSA isolates, we performed random amplified polymorphic DNA analysis with primers Eric II (5´-AAG TAA GTG ACT GGG GTG AGC G-3´), RW3A (5´-TCG CTC AAA ACA ACG ACA CC-3´), D14307 (5´-GGT TGG GTG AGA ATT GCA CG-3´) and spa-typing.
Overall, 3 different MRSA strains were identified. The isolates of the girl (case-patient A), her parents, and the pig from their farm were identical with random amplified polymorphic DNA and belonged to spa-type t108. Furthermore, one of the regional pig farmers screened during the meeting, the pig farmer from a different region (case-patient B), the young boy (case-patient C), as well as his father and the nurse who treated the boy, were colonized with the same strain (Table). Three of the regional pig farmers shared spa-type 567. The isolate from the remaining MRSA-positive regional farmer showed a spa-type not previously described (Table).
Recently, MRSA has been found in horses and in persons who take care of them (4). Human carriage has also been linked to colonized companion cats and dogs (5,6). While Lee et al. (7) reported an MRSA isolation frequency of 0.6% in major food animals, but did not find MRSA in 469 samples from pigs, Armand-Lefevre et al. (8) described S. aureus (methicillin-susceptible and -resistant) carriage among pigs and pig farmers. Although the authors showed that both farmers and pigs carried methicillin-sensitive S. aureus and MRSA and that both groups shared certain multilocus sequence typing, the isolates came from separate, nonrelated collections.
Here we demonstrate transmission of MRSA between an animal and human (pig and pig farmer), between family members (pig farmers and their families), and between a nurse and patient in the hospital. The unexpected high frequency of MRSA among the group of regional pig farmers (>760× higher than in the general Dutch population) indicates that their profession might put them at risk for MRSA colonization. Overall, we found 3 different MRSA strains, including a new spa-type. Therefore, we expect that multiple strains are present in the pig population and the pig farmers. The strain with spa-type t108 appears to be more prevalent and widespread, given that the strain spread from animal to human, between family members, between patient and nurse, and among pig farmers from different regions.
Further research on a larger scale is needed to see if these observations hold true in other regions. If so, pig farming poses a significant risk factor for MRSA carriage in humans that warrants screening wherever pig farmers or their family members are admitted to a hospital.
Dr Voss is a consultant microbiologist and head of infection control at the Canisius-Wilhelmina Hospital and professor of infection control at the Radboud University Medical Centre. His primary research interests are nosocomial infections, including multidrug-resistant nosocomial pathogens such as MRSA.
- Tiemersma EW, Bronzwaer SL, Degener JE, Lyytikäinen O, Schrijnemakers P, Bruinsma N, Methicillin-resistant Staphylococcus aureus in Europe, 1999–2002. Emerg Infect Dis. 2004;10:1627–34.
- Wertheim HF, Vos MC, Boelens HA, Voss A, Vandenbroucke-Grauls CM, Meester MH, Low prevalence of methicillin-resistant Staphylococcus aureus (MRSA) at hospital admission in the Netherlands: the value of search and destroy and restrictive antibiotic use. J Hosp Infect. 2004;56:321–5.
- Reischl U, Linde HJ, Metz M, Leppmeier B, Lehn N. Rapid identification of methicillin-resistant Staphylococcus aureus and simultaneous species confirmation using real-time fluorescence PCR. J Clin Microbiol. 2000;38:2429–33.
- Weese JS, Archambault M, Willey BM, Dick H, Hearn P, Kreiswirth BN, Methicillin-resistant Staphylococcus aureus in horses and horse personnel, 2000–2002. Emerg Infect Dis. 2005;11:430–5.
- Duquette RA, Nuttall TJ. Methicillin-resistant Staphylococcus aureus in dogs and cats: an emerging problem? J Small Anim Pract. 2004;45:591–7.
- Cefai C, Ashurst S, Owens C. Human carriage of methicillin-resistant Staphylococcus aureus linked with pet dog. Lancet. 1994;344:539–40.
- Lee JH. Methicillin (oxacillin)-resistant Staphylococcus aureus strains isolated from major food animals and their potential transmission to humans. Appl Environ Microbiol. 2003;69:6489–94.
- Armand-Lefevre L, Ruimy R, Andremont A. Clonal comparison of Staphylococcus aureus isolates from healthy pig farmers, human controls, and pigs. Emerg Infect Dis. 2005;11:711–4.
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