Absence of LA-MRSA CC398 as nasal colonizer of pigs raised

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AEM Accepts, published online ahead of print on 9 December 2011 Appl. Environ. Microbiol. doi:10.1128/aem.07260-11 Copyright 2011, American Society for Microbiology and/or the Listed Authors/Institutions. All Rights Reserved. 1 2 3 4 5 6 7 8 9 10 11 12 13 14 15 16 17 18 19 20 21 22 23 24 25 26 27 28 29 30 Absence of LA-MRSA CC398 as nasal colonizer of pigs raised in an alternative system Christiane Cuny*, DVM, 1 * Alexander W. Friedrich, MD 2 and Wolfgang Witte, PhD 1 1 Robert Koch Institute, Wernigerode Branch, Wernigerode, Germany 2 Dept. for Med. Microbiology and Infection Control University Hospital Groningen, Groningen, The Netherlands * corresponding author: Christiane Cuny, DVM German National Reference Centre for Staphylococci, Robert Koch Institute, Wernigerode Branch 38855 Wernigerode Germany Phone: 0049-3943-679346 Fax: 0049-3943-679317 cunych@rki.de

31 32 33 34 35 36 37 38 39 40 41 42 Livestock associated MRSA ST398 was reported so far from pigs raised in conventional farms. Here we report a study on 25 farms adhering to an alternative system. LA-MRSA ST398 was not detected in nasal swabs from 178 pigs and also not from 89 humans working and living on these farms. Downloaded from http://aem.asm.org/ on April 10, 2018 by guest

43 44 45 46 47 48 49 50 51 52 53 54 55 56 57 58 59 60 61 62 63 64 65 66 67 68 Methicillin-resistant Staphylococcus aureus (MRSA) are known since the early 1960s, and with a few exceptions they became a frequent nosocomial pathogen by the 1990s worldwide (health care associated MRSA, HA-MRSA [11]). This was followed by the emergence of MRSA infections without any epidemiological association to health care settings during the past 19 years (community associated, CA-MRSA [10]). MRSA particularly associated with livestock (LA-MRSA) nearly exclusively belong to clonal complex CC398 as defined by multilocus sequence typing. They became first known in the Netherlands in 2004 in pigs and were meanwhile reported as nasal colonizer in pigs from many other European countries and from North America, and furthermore from other livestock such as veal calves and chicken (for summary see [2]). Although spread of LA-MRSA CC398 to humans as colonizer is mainly associated with direct exposure to livestock and obviously rare beyond farms (4, 11), infections in humans have been observed which correspond in their clinical presentation to deep seated infections of skin and soft tissue caused by CA-MRSA (3,6). Most studies on LA-MRSA at the farm level were performed in facilities where pigs, veal calves and chicken are raised in an industrial way. As known from studies on HA-MRSA, use of antibacterial drugs is a risk factor for emergence and spread (for a recent meta-analysis see [8]). Very likely this also applies to animals and MRSA CC398. In systems of industrial livestock production animals are not necessarily sick as an indication for treatment. Preventive treatment is often excerted. Furthermore, in case of infection, healthy animals which are together with the diseased ones, get antibiotic supplemented feed at the same time. This is supported by observations by van Duijkeren et al. (13) who found the number of MRSA colonized pigs lower in farms not doing so. LA-MRSA pose an unpredictable future risk to humans. Therefore, the question whether they also appear in alternative production systems and in small, individual keeping of pigs is of particular interest. Here we report on a study on nasal colonization of pigs raised in alternative farm systems.

69 70 71 72 73 74 75 76 77 78 79 80 81 82 83 84 85 86 87 88 89 90 91 92 Different from conventional fattening alternative farms like those of the Neuland association in Germany are usually smaller (less than 600 pigs vs. at the average 3000 pigs in conventional farms), pigs are held on floors with straw bedding with sufficient room for run of the animals. There is no use of antibiotics in pigs with body mass > 25 kg. The systems are closed with respect to imports from conventional systems where often particular farms are specialized for reproduction, others for fattening. Trading of piglets is very likely the route of interfarm dissemination of MRSA (13). Farms visited in the study reported here where located in German Federal countries Lower Saxony, Saxony Anhalt, and Mecklenburg- Western Pomerania where intensive farming is practicised. Nasal swabs were taken from at least 5 pigs at each of the farms and in parallel from humans working and living on these farms. For detection of MRSA swabs were processed as reported previously (4). Results from alternative farms of the Bioland association: nasal swabs from 178 pigs raised at 25 farms were negative for MRSA and also for S. aureus. Among nasal swabs obtained from 89 humans, 31 (34.8%) were positive for methicillin susceptible S. aureus. When subjected to typing as described previously (4) nearly all of these isolates exhibited spa-types typical for S. aureus isolates from nasal colonization of humans and have not been observed among isolates belonging to clonal complex CC398 so far (12) : 1x t127, (clonal complex CC1), 1x t688 (CC5), 1x t211 (CC8), 1x t793 (CC15), 2x t7078 (CC25), 2x t012, 3 x t021, 1x t253, 1x t275, 1x t318, 1x t2387 (CC30), 2x t884 (CC34), 2x t073, 1x t1419, 1x t5529 (CC45), 2x 3397 (CC59), 5x t159 (CC121), 1x t1645 (ST426). Spa types t3446 and t526 are attributed to clonal lineages ST9 and ST97 respectively. ST9 occurs mainly in pigs, occasionally also in humans, and ST97 has been reported from cattle world wide (5). Only one person was tested positive for MRSA CC398 (spa-type t034). This person worked at one of the Neuland farms and was previously employed on a conventional farm.

93 94 95 96 97 98 99 100 101 102 103 104 105 106 107 108 109 110 111 112 113 114 115 116 117 118 Results from 16 individual small keepings of pigs raised for own consumption in villages of a rural area: nasal swabs from 43 pigs kept in backyards were negative as were swabs from 16 human owners. Data from conventional farms for comparison from a study performed previously (4): nasal swabs from pigs (altogether 235) were positive for MRSA in 47 of 57 farms (47 %) visited. From 113 humans exposed to pigs in these farms, 97 (86 %) were positive. Details with respect to typing and antibiotic resistance phenotypes have been reported previously (4). Studies performed before introduction of industrial fattening revealed that S. aureus is only a rare nasal colonizer of domesticated pigs (6). This seems to apply also to free living pigs in general. Thus we were not able to detect S. aureus or MRSA in nasal swabs taken from 120 of wild boars immediately after shooting them in three different geographical areas of Germany. Further studies are needed to address the reasons for the absence of LA-MRSA CC398 in alternative pig production, such as the role of antibiotic treatment and of intimate environmental conditions. Specimen collection, and data processing was approved by the ethical commission of Otto von Guericke University Magdeburg (file # 47/09). References 1. Broens, E.M. et al. 2011.Prevalence and risk factor analysis of livestock associated MRSA-positive pig herds in The Netherlands.Prev. Vet. Med. 102(1):41-9. Epub 2011 Jul 2. Catry, B. 2010. Scientific Advisory Group on Antimicrobials (SAGAM). Reflection paper on MRSA in food-producing and companion animals: epidemiology and control options for human and animal health. Epidemiol Infect. 138:626 644. 3. Cuny, C., and Witte, W. 2008. Importance of the spread of methicillin-resistant Staphylococcus aureus (MRSA) in fattened pigs for humans? MMW Fortschr Med.150 Suppl 2:65 67.

119 120 121 122 123 4. Cuny, C. et al. 2009. Nasal colonization of humans with methicillin-resistant Staphylococcus aureus (MRSA) CC398 with and without exposure to pigs. PLoS One. 2009;4:e6800. 5. Cuny, C. et al. 2010. Emergence of methicillin-resistant Staphylococcus aureus in different animal species. Int J Med Microbiol 300: 109 17. 124 125 126 127 128 129 130 131 132 133 134 135 136 137 138 139 140 141 6. Lewis, H. et al. 2008. Pigs as source of methicillin-resistant Staphylococcus aureus CC398 infections in humans, Denmark. Emerg Infect Dis.14:1383 89. 7.Pulverer, G., and Entel,H.J. 1967. Physiologisches Vorkommen koagulasepositiver Staphylokokken in Tierreich. 1. Nachweis koagulasepositiver Staphylokokken im Rachenraum von Haustieren und wild lebenden Tieren. Zbl Bakt I Orig. 202:344 351. 8. Tacconelli, E., De Angelis, G., Cataldo, M.A., Pozzi, E., Cauda, R. 2008. Does antibiotic exposure incease the risk of methicillin-resistant Staphylococcus aureus (MRSA) isolation? A systematic review and meta-analysis. J Antimicrob Chemother. 61:26 38. 9.. Tiemersma, E.W., et al. 2004.Methicillin-resistant Staphylococcus aureus in Europe, 1999-2002. Emerg Infect Dis. 10:1627 1634. 10. Tristan, A. Et al. 2006. Global distribution of Panton-Valentine leukocidin-positive methicillin-resistant Staphylococcus aureus, Emerg Infect Dis. 13:594 600. 11. van Cleef, B.A., et al. 2010. Prevalence of livestock-associated MRSA in communities with high pig-densities in The Netherlands. PLoS One.5:e9385. 12. van Cleef, B.A. et al. 2011. Livestock-associated methicillin-resistant Staphylococcus aureus from humans, Europe. Emerg Infect Dis 17: 502 5. 13. van Duijkeren, E., et al. 2008. Transmission of methicillin-resistant Staphylococcus aureus strains between different kinds of pig farms. Vet Microbiol. 126:383 389. 142