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Methicillin-Resistant Staphylococcus
                                       aureus in Pork Production Shower
                                       Facilities
                                       Kerry R. Leedom Larson, Abby L. Harper, Blake M. Hanson,
                                       Michael J. Male, Shylo E. Wardyn, Anne E. Dressler,




                                                                                                              Downloaded from http://aem.asm.org/ on December 7, 2011 by The University of Iowa Libraries
                                       Elizabeth A. Wagstrom, Shaliesh Tendolkar, Daniel J.
                                       Diekema, Kelley J. Donham and Tara C. Smith
                                       Appl. Environ. Microbiol. 2011, 77(2):696. DOI:
                                       10.1128/AEM.01128-10.
                                       Published Ahead of Print 19 November 2010.




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                                        http://aem.asm.org/content/77/2/696


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               REFERENCES               This article cites 26 articles, 4 of which can be accessed free at:
                                        http://aem.asm.org/content/77/2/696#ref-list-1

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APPLIED AND ENVIRONMENTAL MICROBIOLOGY, Jan. 2011, p. 696–698                                                                Vol. 77, No. 2
0099-2240/11/$12.00 doi:10.1128/AEM.01128-10
Copyright © 2011, American Society for Microbiology. All Rights Reserved.



                   Methicillin-Resistant Staphylococcus aureus in Pork
                              Production Shower Facilities
           Kerry R. Leedom Larson,1 Abby L. Harper,1,2 Blake M. Hanson,2,3 Michael J. Male,2,3
                      Shylo E. Wardyn,2 Anne E. Dressler,2 Elizabeth A. Wagstrom,4
                              Shaliesh Tendolkar,5,6,7 Daniel J. Diekema,5,6,7




                                                                                                                                              Downloaded from http://aem.asm.org/ on December 7, 2011 by The University of Iowa Libraries
                                Kelley J. Donham,1 and Tara C. Smith2,3*
Department of Occupational and Environmental Health, University of Iowa College of Public Health, Iowa City, Iowa1; Center for
   Emerging Infectious Diseases, University of Iowa College of Public Health, Iowa City, Iowa2; Department of Epidemiology,
    University of Iowa College of Public Health, Iowa City, Iowa3; Center for Animal Health and Food Safety, University of
      Minnesota, St. Paul, Minnesota4; Department of Medicine, University of Iowa Carver College of Medicine, Iowa City,
          Iowa5; Program of Hospital Epidemiology, University of Iowa Hospitals and Clinics, Iowa City, Iowa6; and
                   Department of Pathology, University of Iowa Carver College of Medicine, Iowa City, Iowa7
                                            Received 10 May 2010/Accepted 25 October 2010

           As methicillin-resistant Staphylococcus aureus (MRSA) has been found in pigs, we sought to determine if
         MRSA is present in pork production shower facilities. In two production systems tested, 3% and 26% of shower
         samples were positive for MRSA. spa types identified included t034, t189, t753, and t1746.


   Livestock-associated methicillin-resistant Staphylococcus au-           ducted as previously described (19). At PSA, no MRSA was
reus (LA-MRSA) is a novel pathogen associated with cattle,                 detected in swine nasal swab samples from the first site, and
veal calves, horses, pigs, and poultry (11–13, 15, 16, 19, 22–24,          7/25 (28%) of samples were positive for MRSA from the sec-
26). To date, multilocus sequence type 398 (ST398) has been                ond site. Overall, the prevalence of MRSA in swine at PSA was
most often associated with LA-MRSA. The spa type most                      7/50 (14%). In PSB, 147/209 (70%) of swine nasal swab sam-
commonly associated with ST398 in North America is t034,                   ples were positive for MRSA (19). From PSA, two swine nasal
although up to 24 other associated spa types have been iden-               samples were chosen for additional molecular testing. Both
tified in North America and Europe (21).                                    were negative for the Panton-Valentine leukocidin gene (pvl, a
   ST398 nasal carriage has been identified in people with                  potential virulence gene) (18) and were spa type t1746. Mul-
occupational exposure to swine (4, 6, 12, 17, 19, 26). In the              tilocus sequence typing (MLST) did not identify an established
U.S., ST398 colonization has been reported in two publications             sequence type. From PSB, swine nasal swab samples had been
(2, 19), but environmental reservoirs were not examined in                 previously confirmed as ST398 by MLST (19).
those studies. Locker room and athletic facilities are known                  Shower swabs. In 10 showers, we collected 10 samples each
reservoirs for human MRSA strains (14, 20).                                using sterile swabs (BD BBL culture swabs with Stuart liquid
   Shower-in, shower-out facilities are common in modern                   media; Becton Dickinson and Company) moistened with ster-
pork production systems. Previous research has suggested that              ile phosphate-buffered saline. We focused on areas in the
pork production shower facilities do not harbor MRSA (1);                  showers and changing room that workers contact frequently,
however, the presence of MRSA in pigs on those farms was not               because so-called “hand-touch” sites are frequently contami-
examined. We sought to determine if MRSA can be cultured
                                                                           nated with pathogens in hospitals (5). In PSA, we found one
from showers within production systems known to harbor pigs
                                                                           positive sample from three showers, for an overall prevalence
that yielded MRSA-positive nasal swabs.
                                                                           of 1/30 (3%). The positive sample was taken from clothing
   Two conventional swine production systems were selected
                                                                           hooks on the “dirty” side of the shower changing area, where
for this study in Iowa and Illinois. We sampled two wean-to-
                                                                           employees enter the shower area before accessing the rooms
finish sites with 6,500 pigs each in production system A (PSA).
                                                                           holding pigs. The isolate was pvl negative and spa type t034.
In production system B (PSB), we sampled one 5,200-sow site,
                                                                           Previously, spa type t034 has been associated with ST398 in the
two nursery sites consisting of approximately 15,000 pigs at two
sites, and one 8,000-animal finisher site.                                  Ridom SpaServer database (www.ridom.de).
   Swine nasal swabs. In PSA, prior to shower sampling, pigs at               In PSB, we found 18 positive samples from seven showers,
both wean-to-finish sites were sampled (n 50). In PSB, swine                for an overall prevalence of 18/70 (26%). MRSA-positive sam-
nasal swabs had been previously collected (n           209) (19).          ples were collected from the following sites: shower floor (n
Sampling, bacterial isolation, and molecular typing were con-              5), shower drain (n 3), clean side floor (n 2), locker handle
                                                                           (n     2), shower curtain, shower wall, dirty-side floor, light
                                                                           switch, chair, and soap bottle (one each). All isolates were pvl
  * Corresponding author. Mailing address: University of Iowa Col-         negative. Identified spa types were t034, t1746, t189, and t753.
lege of Public Health, Department of Epidemiology, C21-F GH, 200
Hawkins Drive, Iowa City, IA 52242. Phone: (319) 384-5755. Fax:
                                                                           One sample (spa type t189) was identified as ST188. Novel
(319) 384-5004. E-mail: tara-smith@uiowa.edu.                              sequence types were identified for four samples (spa types 1746
    Published ahead of print on 19 November 2010.                          and 753) (Table 1).

                                                                     696
VOL. 77, 2011                                                                   MRSA IN PORK PRODUCTION SHOWER FACILITIES                                             697


                                    TABLE 1. Characteristics of selected swine nasal swabs and shower swabs
           Production                                                                                                        MLST
Sample                                    Source                     spa type             Repeat sequences                                   Antimicrobial resistancec
             system                                                                                                          typea

  1             A           Nasal, swine                              t1746        07-120-12-23-02-12-23                    Novelb          TET
  2             A           Nasal, swine                              t1746        07-120-12-23-02-12-23                    Novel           TET
  3             A           Locker room hooks (dirty side),           t034         08-16-02-25-02-25-34-24-25                               TET, OXA, CLI
                              wean to finish site
  4             B           Locker room chair (dirty side),           t1746        07-120-12-23-02-12-23                    Novel           TET, OXA
                              sow site




                                                                                                                                                                              Downloaded from http://aem.asm.org/ on December 7, 2011 by The University of Iowa Libraries
  5             B           Shower floor, sow site                     t189         07-23-12-21-17-34                        ST188           None
  6             B           Shower drain, sow site                    t753         08-16-52-25-02-25-34-24-25               Novel           TET, OXA
  7             B           Shower floor, sow site                     t034         08-16-02-25-02-25-34-24-25                               TET, OXA
  8             B           Shower floor, nursery site                 t034         08-16-02-25-02-25-34-24-25                               TET, OXA, CLI, ERY
                                                                                                                                             (intermediate)
 a
   MLST was not performed for spa type t034; ST398 was associated with t034 in previous work (19).
 b
   Allelic profiles of novel sequence types most closely matched that of ST398 in the Ridom SpaServer database.
 c
   TET, tetracycline, OXA, oxacillin, CLI, clindamycin, ERY, erythromycin.



   Eight samples were selected for antimicrobial susceptibility                  No. T42OH008491 from the Centers for Disease Control and Pre-
testing. Five of eight (63%) isolates were resistant to oxacillin,               vention/National Institute for Occupational Safety and Health.
seven (88%) were resistant to tetracycline, and two (25%) were                                                       REFERENCES
resistant to clindamycin (Table 1). Samples that were suscep-                     1. Amass, S. F., R. Jolie, J. L. Schneider, and P. Morgan. 2005. A pilot study
tible to oxacillin by the broth microdilution test were recul-                       to determine the prevalence of methicillin-resistant Staphylococcus aureus in
                                                                                     showers at pork production facilities, gymnasiums, and private residences in
tured on MRSA selective plates and were retested with the                            Indiana. J. Swine Health Prod. 13:150–151.
MRSA latex agglutination test and mecA PCR (3) to ensure                          2. Bhat, M., et al. 2009. Staphylococcus aureus ST398, New York City and
                                                                                     Dominican Republic. Emerg. Infect. Dis. 15:285–287.
that samples were correctly identified as MRSA. Oxacillin-                         3. Bosgelmez-Tinaz, G., S. Ulusoy, B. Aridogan, and F. Coskun-Ari. 2006. Evaluation
susceptible, mecA-positive MRSA has been previously re-                              of different methods to detect oxacillin resistance in Staphylococcus aureus and their
ported (10, 25).                                                                     clinical laboratory utility. Eur. J. Clin. Microbiol. Infect. Dis. 25:410–412.
                                                                                  4. Cui, S., et al. 2009. Isolation and characterization of methicillin-resistant
   spa type t1746 was identified in swine nasal swab samples                          Staphylococcus aureus from swine and workers in China. J. Antimicrob.
from PSA and from a locker room chair in PSB. Upon further                           Chemother. 64:680–683.
testing, a novel sequence type associated with spa type 1746                      5. Dancer, S. J. 2009. The role of environmental cleaning in the control of
                                                                                     hospital-acquired infection. J. Hosp. Infect. 73:378–385.
was found. spa type t189 was isolated from a shower floor at                       6. Denis, O., et al. 2009. Methicillin-resistant Staphylococcus aureus ST398 in
the sow site at PSB. This spa type has previously been associ-                       swine farm personnel, Belgium. Emerg. Infect. Dis. 15:1098–1101.
                                                                                  7. Ghaznavi-Rad, E., et al. 2010. Predominance and emergence of clones of
ated with ST188 (7). Our sample was also identified as ST188                          hospital-acquired methicillin-resistant Staphylococcus aureus in Malaysia.
by MLST. spa type t753 was isolated from a shower drain at the                       J. Clin. Microbiol. 48:867–872.
PSB sow site. A novel ST was identified for this isolate.                          8. Gibbs, S. G., et al. 2006. Isolation of antibiotic-resistant bacteria from the air
                                                                                     plume downwind of a swine confined or concentrated animal feeding oper-
   At site 5, a finishing location in PSB, we observed that                           ation. Environ. Health Perspect. 114:1032–1037.
although 50% of swine sampled were colonized with MRSA,                           9. Green, C. F., S. G. Gibbs, P. M. Tarwater, L. C. Mota, and P. V. Scarpino.
no shower samples were positive. Interestingly, this shower was                      2006. Bacterial plume emanating from the air surrounding swine confine-
                                                                                     ment operations. J. Occup. Environ. Hyg. 3:9–15.
separated from the swine barn, indicating that physical sepa-                    10. Hososaka, Y., et al. 2007. Characterization of oxacillin-susceptible mecA-positive
ration from animals or dust may be important. This arrange-                          Staphylococcus aureus: a new type of MRSA. J. Infect. Chemother. 13:79–86.
                                                                                 11. Juhasz-Kaszanyitzky, E., et al. 2007. MRSA transmission between cows and
ment may also limit airborne spread, which has been previously                       humans. Emerg. Infect. Dis. 13:630–632.
documented for S. aureus in and around swine barns (8, 9).                       12. Khanna, T., R. Friendship, C. Dewey, and J. S. Weese. 2008. Methicillin
   This study had several limitations, including a small sample                      resistant Staphylococcus aureus colonization in pigs and pig farmers. Vet.
                                                                                     Microbiol. 128:298–303.
size. We did not test human workers at the farm. Therefore, we                   13. Leenders, A. C., M. Janssen, N. H. M. Renders, and M. Pelk. 2007. Pig’s
cannot be sure of the relative contributions of MRSA of hu-                          MRSA on a poultry farm? Infectieziekten Bull. 18:43–44.
man versus livestock origin in our positive shower samples.                      14. Montgomery, K., T. J. Ryan, A. Krause, and C. Starkey. 2010. Assessment of
                                                                                     athletic health care facility surfaces for MRSA in the secondary school
Both production systems tested utilize antimicrobials for pro-                       setting. J. Environ. Health 72:8–11.
phylactic and therapeutic reasons. We did not test production                    15. Mooji, R., A. Troelstra, J. M. Jenkins, and S. F. T. Thijsen. 2007. MRSA in
                                                                                     calves. Infectieziekten Bull. 18:236.
systems that abstain from antimicrobial use and therefore can-                   16. Mulders, M. N., et al. 2010. Prevalence of livestock-associated MRSA in
not speculate on antimicrobial use and the finding of MRSA in                         broiler flocks and risk factors for slaughterhouse personnel in The Nether-
showers. Further studies are needed to determine whether                             lands. Epidemiol. Infect. 138:743–755.
                                                                                 17. Neela, V., et al. 2009. Prevalence of ST9 methicillin-resistant Staphylococcus
environmental MRSA reservoirs are associated with an in-                             aureus among pigs and pig handlers in Malaysia. J. Clin. Microbiol. 47:4138–
creased risk of colonization and/or infection in pork produc-                        4140.
tion workers and to determine the most effective methods of                      18. Rasigade, J. P., et al. 2010. Global distribution and evolution of Panton-
                                                                                     Valentine leukocidin-positive methicillin-susceptible Staphylococcus aureus,
MRSA control in the shower environment.                                              1981–2007. J. Infect. Dis. 201:1589–1597.
                                                                                 19. Smith, T. C., et al. 2009. Methicillin-resistant Staphylococcus aureus (MRSA)
                                                                                     strain ST398 is present in Midwestern U.S. swine and swine workers. PLoS
  This research was supported (in part) by a pilot project research                  One 4:e4258.
training grant from the Heartland Center for Occupational Health                 20. Stanforth, B., A. Krause, C. Starkey, and T. J. Ryan. 2010. Prevalence of
and Safety at the University of Iowa. The Heartland Center, an                       community-associated methicillin-resistant Staphylococcus aureus in high
Education and Research Center, is supported by Training Grant                        school wrestling environments. J. Environ. Health 72:12–16.
698       LEEDOM LARSON ET AL.                                                                                                        APPL. ENVIRON. MICROBIOL.

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    imals. Epidemiol. Infect. 138:606–625.                                                 Med. Assoc. 226:580–583.
22. Voss, A., F. Loeffen, J. Bakker, C. Klaassen, and M. Wulf. 2005. Methicillin-      25. Witte, W., B. Pasemann, and C. Cuny. 2007. Detection of low-level oxacillin
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23. Weese, J. S., et al. 2005. Methicillin-resistant Staphylococcus aureus in horses   26. Wulf, M., and A. Voss. 2008. MRSA in livestock animals—an epidemic
    and horse personnel, 2000–2002. Emerg. Infect. Dis. 11:430–435.                        waiting to happen? Clin. Microbiol. Infect. 14:519–521.




                                                                                                                                                                          Downloaded from http://aem.asm.org/ on December 7, 2011 by The University of Iowa Libraries

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Methicillin-resistant Staphylococcus aureus (MRSA) in pork production shower facilities

  • 1. Methicillin-Resistant Staphylococcus aureus in Pork Production Shower Facilities Kerry R. Leedom Larson, Abby L. Harper, Blake M. Hanson, Michael J. Male, Shylo E. Wardyn, Anne E. Dressler, Downloaded from http://aem.asm.org/ on December 7, 2011 by The University of Iowa Libraries Elizabeth A. Wagstrom, Shaliesh Tendolkar, Daniel J. Diekema, Kelley J. Donham and Tara C. Smith Appl. Environ. Microbiol. 2011, 77(2):696. DOI: 10.1128/AEM.01128-10. Published Ahead of Print 19 November 2010. Updated information and services can be found at: http://aem.asm.org/content/77/2/696 These include: REFERENCES This article cites 26 articles, 4 of which can be accessed free at: http://aem.asm.org/content/77/2/696#ref-list-1 CONTENT ALERTS Receive: RSS Feeds, eTOCs, free email alerts (when new articles cite this article), more» Information about commercial reprint orders: http://aem.asm.org/site/misc/reprints.xhtml To subscribe to to another ASM Journal go to: http://journals.asm.org/site/subscriptions/
  • 2. APPLIED AND ENVIRONMENTAL MICROBIOLOGY, Jan. 2011, p. 696–698 Vol. 77, No. 2 0099-2240/11/$12.00 doi:10.1128/AEM.01128-10 Copyright © 2011, American Society for Microbiology. All Rights Reserved. Methicillin-Resistant Staphylococcus aureus in Pork Production Shower Facilities Kerry R. Leedom Larson,1 Abby L. Harper,1,2 Blake M. Hanson,2,3 Michael J. Male,2,3 Shylo E. Wardyn,2 Anne E. Dressler,2 Elizabeth A. Wagstrom,4 Shaliesh Tendolkar,5,6,7 Daniel J. Diekema,5,6,7 Downloaded from http://aem.asm.org/ on December 7, 2011 by The University of Iowa Libraries Kelley J. Donham,1 and Tara C. Smith2,3* Department of Occupational and Environmental Health, University of Iowa College of Public Health, Iowa City, Iowa1; Center for Emerging Infectious Diseases, University of Iowa College of Public Health, Iowa City, Iowa2; Department of Epidemiology, University of Iowa College of Public Health, Iowa City, Iowa3; Center for Animal Health and Food Safety, University of Minnesota, St. Paul, Minnesota4; Department of Medicine, University of Iowa Carver College of Medicine, Iowa City, Iowa5; Program of Hospital Epidemiology, University of Iowa Hospitals and Clinics, Iowa City, Iowa6; and Department of Pathology, University of Iowa Carver College of Medicine, Iowa City, Iowa7 Received 10 May 2010/Accepted 25 October 2010 As methicillin-resistant Staphylococcus aureus (MRSA) has been found in pigs, we sought to determine if MRSA is present in pork production shower facilities. In two production systems tested, 3% and 26% of shower samples were positive for MRSA. spa types identified included t034, t189, t753, and t1746. Livestock-associated methicillin-resistant Staphylococcus au- ducted as previously described (19). At PSA, no MRSA was reus (LA-MRSA) is a novel pathogen associated with cattle, detected in swine nasal swab samples from the first site, and veal calves, horses, pigs, and poultry (11–13, 15, 16, 19, 22–24, 7/25 (28%) of samples were positive for MRSA from the sec- 26). To date, multilocus sequence type 398 (ST398) has been ond site. Overall, the prevalence of MRSA in swine at PSA was most often associated with LA-MRSA. The spa type most 7/50 (14%). In PSB, 147/209 (70%) of swine nasal swab sam- commonly associated with ST398 in North America is t034, ples were positive for MRSA (19). From PSA, two swine nasal although up to 24 other associated spa types have been iden- samples were chosen for additional molecular testing. Both tified in North America and Europe (21). were negative for the Panton-Valentine leukocidin gene (pvl, a ST398 nasal carriage has been identified in people with potential virulence gene) (18) and were spa type t1746. Mul- occupational exposure to swine (4, 6, 12, 17, 19, 26). In the tilocus sequence typing (MLST) did not identify an established U.S., ST398 colonization has been reported in two publications sequence type. From PSB, swine nasal swab samples had been (2, 19), but environmental reservoirs were not examined in previously confirmed as ST398 by MLST (19). those studies. Locker room and athletic facilities are known Shower swabs. In 10 showers, we collected 10 samples each reservoirs for human MRSA strains (14, 20). using sterile swabs (BD BBL culture swabs with Stuart liquid Shower-in, shower-out facilities are common in modern media; Becton Dickinson and Company) moistened with ster- pork production systems. Previous research has suggested that ile phosphate-buffered saline. We focused on areas in the pork production shower facilities do not harbor MRSA (1); showers and changing room that workers contact frequently, however, the presence of MRSA in pigs on those farms was not because so-called “hand-touch” sites are frequently contami- examined. We sought to determine if MRSA can be cultured nated with pathogens in hospitals (5). In PSA, we found one from showers within production systems known to harbor pigs positive sample from three showers, for an overall prevalence that yielded MRSA-positive nasal swabs. of 1/30 (3%). The positive sample was taken from clothing Two conventional swine production systems were selected hooks on the “dirty” side of the shower changing area, where for this study in Iowa and Illinois. We sampled two wean-to- employees enter the shower area before accessing the rooms finish sites with 6,500 pigs each in production system A (PSA). holding pigs. The isolate was pvl negative and spa type t034. In production system B (PSB), we sampled one 5,200-sow site, Previously, spa type t034 has been associated with ST398 in the two nursery sites consisting of approximately 15,000 pigs at two sites, and one 8,000-animal finisher site. Ridom SpaServer database (www.ridom.de). Swine nasal swabs. In PSA, prior to shower sampling, pigs at In PSB, we found 18 positive samples from seven showers, both wean-to-finish sites were sampled (n 50). In PSB, swine for an overall prevalence of 18/70 (26%). MRSA-positive sam- nasal swabs had been previously collected (n 209) (19). ples were collected from the following sites: shower floor (n Sampling, bacterial isolation, and molecular typing were con- 5), shower drain (n 3), clean side floor (n 2), locker handle (n 2), shower curtain, shower wall, dirty-side floor, light switch, chair, and soap bottle (one each). All isolates were pvl * Corresponding author. Mailing address: University of Iowa Col- negative. Identified spa types were t034, t1746, t189, and t753. lege of Public Health, Department of Epidemiology, C21-F GH, 200 Hawkins Drive, Iowa City, IA 52242. Phone: (319) 384-5755. Fax: One sample (spa type t189) was identified as ST188. Novel (319) 384-5004. E-mail: tara-smith@uiowa.edu. sequence types were identified for four samples (spa types 1746 Published ahead of print on 19 November 2010. and 753) (Table 1). 696
  • 3. VOL. 77, 2011 MRSA IN PORK PRODUCTION SHOWER FACILITIES 697 TABLE 1. Characteristics of selected swine nasal swabs and shower swabs Production MLST Sample Source spa type Repeat sequences Antimicrobial resistancec system typea 1 A Nasal, swine t1746 07-120-12-23-02-12-23 Novelb TET 2 A Nasal, swine t1746 07-120-12-23-02-12-23 Novel TET 3 A Locker room hooks (dirty side), t034 08-16-02-25-02-25-34-24-25 TET, OXA, CLI wean to finish site 4 B Locker room chair (dirty side), t1746 07-120-12-23-02-12-23 Novel TET, OXA sow site Downloaded from http://aem.asm.org/ on December 7, 2011 by The University of Iowa Libraries 5 B Shower floor, sow site t189 07-23-12-21-17-34 ST188 None 6 B Shower drain, sow site t753 08-16-52-25-02-25-34-24-25 Novel TET, OXA 7 B Shower floor, sow site t034 08-16-02-25-02-25-34-24-25 TET, OXA 8 B Shower floor, nursery site t034 08-16-02-25-02-25-34-24-25 TET, OXA, CLI, ERY (intermediate) a MLST was not performed for spa type t034; ST398 was associated with t034 in previous work (19). b Allelic profiles of novel sequence types most closely matched that of ST398 in the Ridom SpaServer database. c TET, tetracycline, OXA, oxacillin, CLI, clindamycin, ERY, erythromycin. Eight samples were selected for antimicrobial susceptibility No. T42OH008491 from the Centers for Disease Control and Pre- testing. Five of eight (63%) isolates were resistant to oxacillin, vention/National Institute for Occupational Safety and Health. seven (88%) were resistant to tetracycline, and two (25%) were REFERENCES resistant to clindamycin (Table 1). Samples that were suscep- 1. Amass, S. F., R. Jolie, J. L. Schneider, and P. Morgan. 2005. A pilot study tible to oxacillin by the broth microdilution test were recul- to determine the prevalence of methicillin-resistant Staphylococcus aureus in showers at pork production facilities, gymnasiums, and private residences in tured on MRSA selective plates and were retested with the Indiana. J. Swine Health Prod. 13:150–151. MRSA latex agglutination test and mecA PCR (3) to ensure 2. Bhat, M., et al. 2009. Staphylococcus aureus ST398, New York City and Dominican Republic. Emerg. Infect. Dis. 15:285–287. that samples were correctly identified as MRSA. Oxacillin- 3. Bosgelmez-Tinaz, G., S. Ulusoy, B. Aridogan, and F. Coskun-Ari. 2006. Evaluation susceptible, mecA-positive MRSA has been previously re- of different methods to detect oxacillin resistance in Staphylococcus aureus and their ported (10, 25). clinical laboratory utility. Eur. J. Clin. Microbiol. Infect. Dis. 25:410–412. 4. Cui, S., et al. 2009. Isolation and characterization of methicillin-resistant spa type t1746 was identified in swine nasal swab samples Staphylococcus aureus from swine and workers in China. J. Antimicrob. from PSA and from a locker room chair in PSB. Upon further Chemother. 64:680–683. testing, a novel sequence type associated with spa type 1746 5. Dancer, S. J. 2009. The role of environmental cleaning in the control of hospital-acquired infection. J. Hosp. Infect. 73:378–385. was found. spa type t189 was isolated from a shower floor at 6. Denis, O., et al. 2009. Methicillin-resistant Staphylococcus aureus ST398 in the sow site at PSB. This spa type has previously been associ- swine farm personnel, Belgium. Emerg. Infect. Dis. 15:1098–1101. 7. Ghaznavi-Rad, E., et al. 2010. Predominance and emergence of clones of ated with ST188 (7). Our sample was also identified as ST188 hospital-acquired methicillin-resistant Staphylococcus aureus in Malaysia. by MLST. spa type t753 was isolated from a shower drain at the J. Clin. Microbiol. 48:867–872. PSB sow site. A novel ST was identified for this isolate. 8. Gibbs, S. G., et al. 2006. Isolation of antibiotic-resistant bacteria from the air plume downwind of a swine confined or concentrated animal feeding oper- At site 5, a finishing location in PSB, we observed that ation. Environ. Health Perspect. 114:1032–1037. although 50% of swine sampled were colonized with MRSA, 9. Green, C. F., S. G. Gibbs, P. M. Tarwater, L. C. Mota, and P. V. Scarpino. no shower samples were positive. Interestingly, this shower was 2006. Bacterial plume emanating from the air surrounding swine confine- ment operations. J. Occup. Environ. Hyg. 3:9–15. separated from the swine barn, indicating that physical sepa- 10. Hososaka, Y., et al. 2007. Characterization of oxacillin-susceptible mecA-positive ration from animals or dust may be important. This arrange- Staphylococcus aureus: a new type of MRSA. J. Infect. Chemother. 13:79–86. 11. Juhasz-Kaszanyitzky, E., et al. 2007. MRSA transmission between cows and ment may also limit airborne spread, which has been previously humans. Emerg. Infect. Dis. 13:630–632. documented for S. aureus in and around swine barns (8, 9). 12. Khanna, T., R. Friendship, C. Dewey, and J. S. Weese. 2008. Methicillin This study had several limitations, including a small sample resistant Staphylococcus aureus colonization in pigs and pig farmers. Vet. Microbiol. 128:298–303. size. We did not test human workers at the farm. Therefore, we 13. Leenders, A. C., M. Janssen, N. H. M. Renders, and M. Pelk. 2007. Pig’s cannot be sure of the relative contributions of MRSA of hu- MRSA on a poultry farm? Infectieziekten Bull. 18:43–44. man versus livestock origin in our positive shower samples. 14. Montgomery, K., T. J. Ryan, A. Krause, and C. Starkey. 2010. Assessment of athletic health care facility surfaces for MRSA in the secondary school Both production systems tested utilize antimicrobials for pro- setting. J. Environ. Health 72:8–11. phylactic and therapeutic reasons. We did not test production 15. Mooji, R., A. Troelstra, J. M. Jenkins, and S. F. T. Thijsen. 2007. MRSA in calves. Infectieziekten Bull. 18:236. systems that abstain from antimicrobial use and therefore can- 16. Mulders, M. N., et al. 2010. Prevalence of livestock-associated MRSA in not speculate on antimicrobial use and the finding of MRSA in broiler flocks and risk factors for slaughterhouse personnel in The Nether- showers. Further studies are needed to determine whether lands. Epidemiol. Infect. 138:743–755. 17. Neela, V., et al. 2009. Prevalence of ST9 methicillin-resistant Staphylococcus environmental MRSA reservoirs are associated with an in- aureus among pigs and pig handlers in Malaysia. J. Clin. Microbiol. 47:4138– creased risk of colonization and/or infection in pork produc- 4140. tion workers and to determine the most effective methods of 18. Rasigade, J. P., et al. 2010. Global distribution and evolution of Panton- Valentine leukocidin-positive methicillin-susceptible Staphylococcus aureus, MRSA control in the shower environment. 1981–2007. J. Infect. Dis. 201:1589–1597. 19. Smith, T. C., et al. 2009. Methicillin-resistant Staphylococcus aureus (MRSA) strain ST398 is present in Midwestern U.S. swine and swine workers. PLoS This research was supported (in part) by a pilot project research One 4:e4258. training grant from the Heartland Center for Occupational Health 20. Stanforth, B., A. Krause, C. Starkey, and T. J. Ryan. 2010. Prevalence of and Safety at the University of Iowa. The Heartland Center, an community-associated methicillin-resistant Staphylococcus aureus in high Education and Research Center, is supported by Training Grant school wrestling environments. J. Environ. Health 72:12–16.
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