The mechanisms of antibiotic resistance in major pathogens of purulent-inflammatory complications in cancer patients
- Authors: Khokhlova O.Е.1, Larionova I.A.2, Perianova O.V.1, Kozlov R.S.3, Eidelshtein M.V.3, Modestov A.A.4, Eremeeva O.G.4, Lazareva I.V.5, Akusheva D.N.1, Lobova T.I.1, Potkina N.K.6, Sidorenko S.V.5, Yamamoto T7,8
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Affiliations:
- Krasnoyarsk State Medical University named after professor V.F. Voyno-Yasenetsky
- Krasnoyarsk State Medical University named after professor V.F. Voyno-Yasenetsky, Krasnoyarsk
- Smolensk State Medical University, Ministry of Health of Russia
- Krasnoyarsk Regional Clinical Oncology Center named after A.I. Kryzhanovsky
- Research Institute for Children's Infections of the Federal Medical and Biological Agency
- Russia-Japan Center of Microbiology, Мetagenomics and Infectious Diseases, Krasnoyarsk State Medical University
- International Medical Education and Research Center
- Russia-Japan Center of Microbiology, Мetagenomics and Infectious Diseases
- Issue: Vol 11, No 2 (2021)
- Pages: 324-336
- Section: ORIGINAL ARTICLES
- Submitted: 14.02.2020
- Accepted: 03.06.2020
- Published: 29.06.2020
- URL: https://iimmun.ru/iimm/article/view/1379
- DOI: https://doi.org/10.15789/2220-7619-TMO-1379
- ID: 1379
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Full Text
Abstract
The problem of microbial antibiotic resistance and investigation of its underlying mechanisms is of paramount importance for all fields of clinical medicine, including oncology. The aim of the study was to examine the mechanisms of antibiotic resistance for major pathogens causing purulent-inflammatory complications in cancer patients. Materials and methods. In 2012—2015 there was conducted a prospective examination of 184 cancer patients, including 67 patients at the Department of Surgery no. 1 and 117 patients at the Intensive Care Unit of the Krasnoyarsk Regional Clinical Oncology Center named after A.I. Kryzhanovsky. For this, we collected bronchoalveolar lavage fluid, wound discharge and investigated the material by using bacteriological method, as well as MALDI-TOF. Antibiotic sensitivity was studied as follows: disco-diffusion, double disc method, carbapenem inactivation method, staphylococcal sensitivity — by screening method, PCR, E-test method, and serial dilutions in Muller-Hinton broth. Genotyping and antibiotic resistance mechanisms study were performed by using PCR, M-PCR, and sequencing. The WHONET program (WHO) was used, with significance level set at p < 0.05. Results. Microbiological examination of bronchoalveolar lavage fluid and wound discharge samples allowed to uncover prevalent associations of multi-resistant (MDR) and extremely resistant pathogens (XDR). The microflora of the lower respiratory tract and in the wound secretion in cancer patients were found to be dominated by non-fermenting Gram-negative bacteria reaching up to 44.5% and 48%, respectively; as well as order Enterobacteriales found in 24% and 34.9%, respectively; Gram-positive bacteria — 24% and 17.1%, respectively. Imipenem- and/or meropenem-resistant P. aeruginosa and A. baumannii, K. pneumoniae strains, were assessed for MBL production phenotypically, as well as the genes of the most common VIM, IMP types, whereas A. baumannii — for OXA-23, OXA-40, and OXA-58; and K. pneumoniae — for OXA-48. 20 strains and 16 strains of P. aeruginosa and A. baumannii, respectively, were studied by PCR. It was found that A. baumannii strains formed no MBL, but 56.3% of A. baumannii isolates (9 strains) produced OXA-23 and OXA-40 carbapenemases. Among P. aeruginosa strains there were three of them which possessed VIM (15.0%), whereas the remaining strains formed no MBL, but were resistant to carbapenems being associated with other resistance mechanisms, e.g. efflux, decreased permeability of cell wall etc. Among 6 isolates of K. pneumoniae, 1 strain produced OXA-48. In cancer patients, the percentage of methicillin-resistant strains among all members of the genus Staphylococcus was 48.9% (4 strains belonged to MRSA). PVL- MRSA strains belonged to the clones ST239/spa3(t037)/SCCmecIIIA/tst,sek,seq+ (75%) and ST8/ spa1(t008)/SCCmecIVc/sea+ (25%). MRSA ST239 showed multiple antibiotic resistance: to aminoglycosides (aacA-aphD, aadD genes were detected), linkcosamides/macrolides (the ermA gene was detected), fluoroquinolones (mutations in the GyrA gene — Ser84Leu; in GrlA- Ser80Phe), rifampicin (MIC more than 128 gg/ml; mutations in the rpoB gene are His481Asn, Ile527Met), sulfamethoxazole, tetracycline (tetM gene), and chloramphenicol (66.7% of isolates, the cat gene encoding chloramphenicol acetyl transferase was detected); but sensitive to vancomycin (MIC 1.0 gg/ ml), linezolid in 100% of cases. MRSA ST8 are resistant to aminoglycosides (aacA-aphD, aadD genes), lincosamides/macrolides (ermC gene), tetracyclines (tetK gene), chloramphenicol (cat gene); and 100% sensitive to fluoroquinolones, rifampicin (MIC 0.006 gg/ml), sulfamethaxazole, vancomycin (MIC 1.0 gg/ml), daptomycin (MIC 0.094 gg/ml), linezolid (MIC 0.75 gg/ml). Conclusion. Thus, it was found that members of the order Enterobacteriales, A. baumannii, P. aeruginosa and MRSA retain high resistance to a large number of antibacterial drugs of almost all classes. These data should be taken into account while choosing proper antibiotic therapy, as well as controlling spread of nosocomial infections caused by multiresistant microorganisms.
About the authors
O. Е. Khokhlova
Krasnoyarsk State Medical University named after professor V.F. Voyno-Yasenetsky
Author for correspondence.
Email: khokhlovaol@mail.ru
ORCID iD: 0000-0002-2829-5117
Olga E. Khokhlova - Ph.D., Associate Professor Department of Microbiology named after Assoc. B.M. Zelmanovich.
660022, Krasnoyarsk, Partizan Zheleznyak str., 1.
Phone: +7 (391) 220-13-61 (office); +7 (908) 018-99-84 (mobile)
РоссияI. A. Larionova
Krasnoyarsk State Medical University named after professor V.F. Voyno-Yasenetsky, Krasnoyarsk
Email: vova_lar@mail.ru
Senior Lecturer, Department of Microbiology named after B.M. Zelmanovitch, Krasnoyarsk State Medical University named after professor V.F. Voyno-Yasenetsky.
660022, Krasnoyarsk, str. Partizan Zheleznyak, 1.
Tel.: 8 908 018 99 84, tel. +7 (391) 220-13-61
РоссияO. V. Perianova
Krasnoyarsk State Medical University named after professor V.F. Voyno-Yasenetsky
Email: perianova@mail.ru
PhD (Biology), Head of the Department of Microbiology named after B.M. Zelmanovitch.
660022, Krasnoyarsk, str. Partizan Zheleznyak, 1.
Tel.: +7 (391) 220-13-61, 8 913 569 83 68
РоссияR. S. Kozlov
Smolensk State Medical University, Ministry of Health of Russia
Email: roman.kozlov@antibiotic.ru
PhD, MD (Medicine), Professor, RAS Full Member, Rector of Smolensk State Medical University.
214019, Smolensk, str. Krupskaya, 28.
Tel.: +7 (481) 255 02 75
РоссияM. V. Eidelshtein
Smolensk State Medical University, Ministry of Health of Russia
Email: adm@smolgmu.ru
PhD (Biology), Head of the Laboratory of the Research Institute of Antimicrobial Chemotherapy, Smolensk State Medical University.
214019, Smolensk Region, Smolensk, str. Krupskaya, 28.
Tel.:+7 (481) 255 02 75
РоссияA. A. Modestov
Krasnoyarsk Regional Clinical Oncology Center named after A.I. Kryzhanovsky
Email: priem@onkolog24.ru
PhD (Medicine), Chief Doctor, Krasnoyarsk Regional Clinical Oncology Center named after A.I. Kryzhanovsky.
660133 Krasnoyarsk Territory, Krasnoyarsk, str. 1st Smolenskaya, 16.
Tel.: 222-40-01
РоссияO. G. Eremeeva
Krasnoyarsk Regional Clinical Oncology Center named after A.I. Kryzhanovsky
Email: priem@onkolog24.ru
Intensivist, Head of the Intensive Care Unit, Krasnoyarsk Regional Clinical Oncology Center named after A.I. Kryzhanovskyю
660133 Krasnoyarsk Territory, Krasnoyarsk, str. 1st Smolenskaya, 16ю
Tel.: 222-40-01
РоссияI. V. Lazareva
Research Institute for Children's Infections of the Federal Medical and Biological Agency
Email: partina-irina@yandex.ru
Researcher, Department of Medical Microbiology and Molecular Epidemiology, Research Institute for Children's Infections of the Federal Medical and Biological Agency.
197022, St. Petersburg.
РоссияD. N. Akusheva
Krasnoyarsk State Medical University named after professor V.F. Voyno-Yasenetsky
Email: kalllissto@yandex.ru
Lecturer, Department of Microbiology named after B.M. Zelmanovitch, Krasnoyarsk State Medical University named after professor V.F. Voyno-Yasenetsky.
660022, Krasnoyarsk, str. Partizan Zheleznyak, 1.
РоссияT. I. Lobova
Krasnoyarsk State Medical University named after professor V.F. Voyno-Yasenetsky
Email: yani.lobv@gmail.com
PhD (Biology), Senior Lecturer, Department of Microbiology named after B.M. Zelmanovitch, Krasnoyarsk State Medical University named after professor V.F. Voyno-Yasenetsky.
660022, Krasnoyarsk, str. Partizan Zheleznyak, 1.
РоссияN. K. Potkina
Russia-Japan Center of Microbiology, Мetagenomics and Infectious Diseases, Krasnoyarsk State Medical University
Email: potnad@mail.ru
Researcher, Russia-Japan Center of Microbiology, Metagenomics and Infectious Diseases, Krasnoyarsk State Medical University.
660022, Krasnoyarsk, str. Partizan Zheleznyak, 1.
Tel.: 8 950 401 97 7
РоссияS. V. Sidorenko
Research Institute for Children's Infections of the Federal Medical and Biological Agency
Email: sidorserg@gmail.com
PhD, MD (Medicine), Professor, Head of the Department of Medical Microbiology and Molecular Epidemiology, Research Institute for Children's Infections of the Federal Medical and Biological Agency.
197022, St. Petersburg, str. Professor Popov, 9.
Tel.: +7 (812) 234-16-70
РоссияT Yamamoto
International Medical Education and Research Center; Russia-Japan Center of Microbiology, Мetagenomics and Infectious Diseases
Email: tatsuoy@imerc.jp
PhD (Medicine), Professor, Director of the International Medical Education and Research Center; Curator of the Russia-Japan Center of Microbiology, Metagenomics and Infectious Diseases, Krasnoyarsk State Medical University.
Niigata; Krasnoyarsk.
ЯпонияReferences
- Белоусова Т.А. Инфекционные осложнения в колоректальной хирургии // Вопросы онкологии. 2012. Т. 58, № 6. С. 736—743.
- Григорьевская З.В., Петухова И.Н., Багирова Н.С., Шильникова И.И., Терещенко И.В., Григорьевский Е.Д., Дмитриева Н.В. Нозокомиальные инфекции у онкологических больных: проблема нарастающей резистентности грамотрицательных микроорганизмов // Сибирский онкологический журнал. 2017. Т. 16, № 1. С. 91—97.
- Давыдов М.И., Дмитриева Н.В. Инфекции в онкологии. М.: Практическая медицина, 2009. 472 с.
- Дмитриева Н.В., Петухова И.Н. Инфекционные осложнения в онкологической клинике // Практическая онкология. 2001. Т. 2, № 1 (5). С. 18-20.
- Дмитриева Н.В., Эйдельштейн М.В., Агинова В.В., Григорьевская З.В., Петухова И.Н., Терещенко И.В., Багирова Н.С., Дьякова С.А., Калинчук Т.А., Дмитриева А.И., Шек Е.А., Склеенова Е.Ю. Инфекции, вызванные Acinetobacter bau-mannii, у онкологических больных // Сибирский онкологический журнал. 2019. Т. 18, № (3). С. 26-33.
- Дрие Л., Броссье Ф., Сугаков В., Жарлье В. Фенотипическое определение Enterobacter — продуцентов в-лактамаз расширенного спектра: обзор и руководство по проведению испытаний // Клиническая микробиология и инфекционные заболевания. 2008. Т. 14 (Прил. 1). С. 90-103.
- Карабак В.И. Микробиологический мониторинг за возбудителями нозокомиальных инфекций (на примере отделений реанимации и интенсивной терапии) // Антибиотики и химиотерапия. 2000. Т. 45, № 3. С. 20-23.
- Лазарева И.В., Агеевец В.А., Ершова Т.А., Зуева Л.П., Гончаров А.Е., Дарьина М.Г., Светличная Ю.С., Усков А.Н., Сидоренко С.В. Распространение и антибактериальная резистентность грамотрицательных бактерий, продуцентов карбапенемаз, в Санкт-Петербурге и некоторых других регионах Российской Федерации // Антибиотики и химиотерапия. 2000. Т. 61. С. 11-12.
- Практическое руководство по антиинфекционной химиотерапии / Под ред. Л.С. Страчунского, Ю.Б. Белоусова, С.Н. Козлова. 2007. URL: http://www.antibiotic.ru/ab/index.shtml (25.11.2020)
- Сидоренко С.В., Резван С.П., Еремина Л.В. Этиология тяжелых госпитальных инфекций в отделениях реанимации и антибиотикорезистентность среди их возбудителей // Антибиотики и химиотерапия. 2005, Т. 50, № 2-3. С. 33-41.
- Туркутюков В.Б. Молекулярно-генетический мониторинг резистентности микроорганизмов к антибиотикам // Тихоокеанский медицинский журнал. 2011. № 2. С. 28-31.
- Хирургические инфекции: руководство / Под ред. И.А. Ерюхина, Б.Р. Гельфанда, С.А. Шляпникова. СПб.: Питер, 2003. 864 с.
- Хохлова О.Е., Перьянова О.В., Боброва О.П., Сергеева В.В., Модестов А.А., Еремеева О.Г., Поткина Н.К., Капшук Д.Н., Алабушева А.В., Дыхно Ю.А., Ямамото Т. Микробиологический мониторинг гнойных осложнений у онкологических больных // Вопросы онкологии. 2018. Т. 64, № 1. С. 121-125.
- Яковлев С.В. Госпитальные инфекции, вызванные резистентными грамотрицательными микроорганизмами, клиническое значение и современные возможности терапии // Инфекции и антимикробная терапия. 2004. Т. 6, № 4. С. 133-136.
- Akiyoshi T., Ueno M., Fukunaga Y., Nagayama S., Fujimoto Y., Konishi T., Kuroyanagi H., Yamaguchi T. Effect of body mass index on short-term outcomes of patients undergoing laparoscopic resection for colorectal cancer: a single institution experience in Japan. Surg. Laparosc. Endosc. Percutan. Tech., 2011, vol. 21, pp. 409—414. doi: 10.1097/SLE.0b013e31822e5fdc
- Alberti C., Brun-Buisson C., Burchardi H., Martin C., Goodman S., Artigas A., Sicignano A., Palazzo M., Moreno R., Boulme R., Lepage E., Gall Le R. Epidemiology of sepsis and infection in ICU patients from an international multicentre cohort study. Intens. Care Med, 2002, vol. 28, pp. 108-121. doi: 10.1007/s00134-001-1143-z
- Avritscher E.B., Cooksley C.D., Rolston K.V., Swint J.M., Delclos G.L., Franzini L., Swisher S.G., Walsh G.L., Mansfield P.F., Elting L.S. Serious postoperative infections following resection of common solid tumors: outcomes, costs, and impact of hospital surgical volume. Support. Care Cancer, 2014, no. 22, pp. 527-535. doi: 10.1007/s00520-013-2006-1
- Choi S.M., Kim S.H., Kim H.J., Lee D.G., Choi J.H., Yoo J.H., Kang J.H., Shin W.S., Kang M.W. Multiplex PCR for the detection of genes encoding aminoglycoside modifying enzymes and methicillin resistance among Staphylococcus species. J. Korean Med. Sci., 2003, vol. 18, no. 5, pp. 631-636. doi: 10.3346/jkms.2003.18.5.631
- David M.Z., Daum R.S. Community-associated methicillin-resistant Staphylococcus aureus: epidemiology and clinical consequences of an emerging epidemic. Clin. Microbiol. Rev., 2010, vol. 23, no. 3, pp. 616-687. doi: 10.1128/CMR.00081-09
- Ellington M.J., Hope R., Livermore D.M., Kearns A.M., Henderson K., Cookson B.D., Pearson A., Johnson A.P. Decline of EMRSA-16 amongst methicillin-resistant Staphylococcus aureus causing bacteraemias in the UK between 2001 and 2007. J. Antimicrob. Chemother., 2010, vol. 65, no. 3, pp. 446-448. doi: 10.1093/jac/dkp448
- Evans B.A., Amyes S.G. OXA Р-Lactamases. Clin. Microbiol. Rev, 2014, vol. 27, no. 2, pp. 241-263. doi: 10.1128/CMR.00117-13
- Fagon J.Y., Chastre J., Vuagnat A., Trouillet J.L., Novara A., Gibert C. Nosocomial pneumonia and mortality among patients in intensive care units. JAMA, 1996, vol. 275, no. 11, pp. 866-869. doi: 10.1001/jama.1996.03530350048033
- Falagas M.E., Bakossi A., Pappas V.D., Holevas P.V., Bouras A., Stamata E. Secular trends of blood isolates in patients from a rural area population hospitalized in a tertiary center in a small city in Greece. BMC Microbiol., 2006, vol. 6, no. 1: 41. doi: 10.1186/14712180-6-41
- International Working Group on the Classification of Staphylococcal Cassette Chromosome Elements (IWG-SCC). Classification of staphylococcal cassette chromosome mec (SCCmec): guidelines for reporting novel SCCmec elements. Agents Chemother., 2009, vol. 53, pp. 4961-4967. doi: 10.1128/AAC.00579-09
- Johnson A.P., Pearson A., Duckworth G. Surveillance and epidemiology of MRSA bacteraemia in the UK. J. Antimicrob. Chemother., 2005, vol. 56, no. 3, pp. 455-462. doi: 10.1093/jac/dki266
- Khokhlova O.E., Hung W.C., Wan T.W., Iwao Y., Takano T., Higuchi W., Yachenko S.V., Teplyakova O.V., Kamshilova V.V., Kotlovsky Y.V., Nishiyama A., Reva I.V., Sidorenko S.V., Peryanova O.V., Reva G.V., Teng L.J., Salmina A.B., Yamamoto T. Healthcare- and community-associated methicillin-resistant Staphylococcus aureus (MRSA) and fatal pneumonia with pediatric deaths in Krasnoyarsk, Siberian Russia: unique MRSA's multiple virulence factors, genome, and stepwise evolution. PLoS One, 2015, vol. 1, pp. 1-30. doi: 10.1371/journal.pone.0128017
- Kondo Y., Ito T., Ma X.X., Watanabe S., Kreiswirth B.N., Etienne J., Hiramatsu K. Combination of multiplex PCRs for staphylococcal cassette chromosome mec type assignment: rapid identification system for mec, ccr, and major differences in junkyard regions. Antimicrob. Agents Chemother., 2007, vol. 51, pp. 264-274. doi: 10.1128/AAC.00165-06
- Lee H.G., Jang J., Choi J.E. Blood stream infections in patients in the burn intensive care unit. Infect. Chemother., 2013, vol. 45, no. 2, pp. 194-201. doi: 10.3947/ic.2013.45.2.194
- Mandel G.L. Principles and practice of infections diseases. 9th ed. London: Churchill Livingstone, 2019. 4176 р.
- Mariani-Kurkdjian P., Doit C., Bingen E. Extended-spectrum beta-lactamase producing-enterobacteriaceae. Arch. Pediatr., 2012, no. 3, pp. 93-96. doi: 10.1016/S0929-693X(12)71280-0
- Martineau F., Picard F.J., Lansac N., Menard C., Roy P.H., Ouellette M., Bergeron M.G. Correlation between the resistance genotype determined by multiplex PCR assays and the antibiotic susceptibility patterns of Staphylococcus aureus and Staphylococcus epidermidis. Antimicrob. Agents Chemother., 2000, vol. 44, no. 2, pp. 231-238. doi: 10.1128/aac.44.2.231-238.2000
- McManus B.A., Coleman D.C., Deasy E.C., Brennan G.I., Connell B.O., Monecke S., Ehricht R., Leggett B., Leonard N., Shore A.C. Comparative genotypes, staphylococcal cassette chromosome mec (sccmec) genes and antimicrobial resistance amongst Staphylococcus epidermidis and Staphylococcus haemolyticus isolates from infections in humans and companion animals. PLoS One, 2015, no. 9, pp. 1-18. doi: 10.1371/journal.pone.0138079
- Peleg A.Y., Seifert H., Paterson D.L. Acinetobacter baumannii: emergence of a successful pathogen. Clin. Microbiol. Rev., 2008, no. 21, pp. 538-582. doi: 10.1128/CMR.00058-07
- Pulcini C., Binda F., Lamkang A.S., Trett A., Charani E. Developing core elements in checklist items fro global hospital antimicrobial stewardship programmes: a consensus approach. Clin. Microbiol. Inf., 2019, vol. 25, no. 1, pp. 20-25. doi: 10.1016/j.cmi.2018.03.033
- Ray S., Anand D., Purwar S., Samanta A., Upadhey K.V. Association of high mortility with extended-spectrum-beta-lacta-mases (ESBL) positive cultures in community aquired infections. J. Critical Care, 2018, no. 44, pp. 255-260. doi: 10.1016/j.jcrc.2017.10.036
- Rolston K.V., Nesher L., Tarrand T.J. Current microbiology of surgical site infections in patients with cancer: a retrospective review. Inf. Dis. Ther., 2014, no. 3, pp. 245-256. doi: 10.1007/s40121-014-0048-4
- Takano T., Higuchi W., Zaraket H., Otsuka T., Baranovich T., Enany S., Saito K., Isobe H., Dohmae S., Ozaki K., Takano M., Iwao Y., Shibuya M., Okubo T., Yabe S., Shi D., Reva I., Teng L.J., Yamamoto T. Novel characteristics of community-acquired methicillin-resistant Staphylococcus aureus strains belonging to multilocus sequence type 59 in Taiwan. Antimicrob. Agents Chemother., 2012, vol. 56, no. 12, pp. 6441-6441. doi: 10.1128/AAC.01001-07
- Takano T., Hung W.C., Shibuya M., Higuchi W., Iwao Y., Nishiyama A., Reva I., Khokhlova O.E., Yabe S., Ozaki K., Takano M., Yamamoto T. A new local variant (ST764) of the globall y disseminated ST5 lineage of hospital-associated methicillin-resistant Staphylococcus aureus (MRSA) carrying the virulence determinants of community-associated MRSA. Antimicrob. Agents Chemother. 2013, vol. 57, pp. 1589-1595. doi: 10.1128/AAC.01147-12
- Unal S., Garcia-Rodriguez J.A. Activity of meropenem and comparators against Pseudomonas aeruginosa and Acinetobacter spp. Isolated in the MYSTIC Program, 2002—2004. Diagn. Microbiol. Infect. Dis., 2005, vol. 53, no. 4, pp. 256—271. doi: 10.1016/j.diagmicrobio.2005.10.002
- Warnes S.L., Highmore C.J., Keevil C.W. Horizontal transfer of antibiotic resistance genes on abiotic touch surfaces: implications for public health. mBio, 2012, vol. 3, no. 6, pp. 489—501. doi: 10.1128/mBio.00489-12
- Wilson H., Torok M.E. Extended-spectrum-beta-lactamases-producing and carbapenem-producing Enterobacteriaceae. Microb. Genom., 2018, vol. 4, pp. 1—14. doi: 10.1099/mgen.0.000218
- Zwaluw K. van der, Haan A. de, Pluister G.N., Bootsma H.J., Neeling A.J. de, Schouls L.M. The carbapenem inactivation method (CIM), a simple and low-cost alternative for the Carba NP test to assess phenotypic carbapenemase activity in gram-negative rods. PLoS One, 2015, vol. 10, no. 3: e0123690. doi: 10.1371/journal.pone.0123690