Антагонистическая активность консорциума штаммов Lactobacillusfermentum ВКМ В-2793D и Lactobacillusreuteri ВКМ В-3144D, выделенных из женского молока, к мастит-индуцирующим патогенам
Аннотация
Об авторах
В. М. АбрамовРоссия
В. С. Хлебников
Россия
И. В. Косарев
Россия
Т. В. Припутневич
Россия
Л. А. Любасовская
Россия
Р. Н. Василенко
Россия
В. К. Сакулин
Россия
В. Н. Каркищенко
Россия
Н. Н. Каркищенко
Россия
С. Ю. Пчелинцев
Россия
А. В. Карлышев
Россия
В. А. Самойленко
Россия
А. В. Мачулин
Россия
Список литературы
1. Руководство по проведению доклинических исследований лекарственных средств (иммунобиологические лекарственные препараты). Ч. 2 / Под ред. А.Н. Миронова. - М.: Гриф и К. - 2012. - 536 с.
2. Brouillette E., Talbot B., Malouin F. The fibronectin-binding proteins of Staphulococcus aureus may promote mammary gland colonization in a lactating mouse model of Mastitis // Infect. Immun. 2003. V. 71. No. 4. Pp. 2292-2295.
3. Brouillette E., Martinez A., Boyll B., et al. Persistence of a Staphylococcus aureus Small-colony variant under antibiotic pressure in vivo // FEMS Immunol. and med. microbiol. 2004. V. 41. Issue 1. Pp. 35-41.
4. Delgado S., Arroyo R., Jiménez E., et al. Staphylococcus epidermidis strains isolated from breast milk of women suffering infectious mastitis: potential virulence traits and resistance to antibiotics // BMC Microbiol. 2009. V. 9. Pp. 82-85.
5. Delgado S., Arroyo R., Jiménez E., et al. Infectious mastitis during lactation: an underrated condition (I) // Acta Pediatrica Espanola. 2009. V. 67. Pp. 77-84.
6. Delgado S., Garcia P., Fernandez L., Jimenez E., Rodriguez-Banos M., Del Campo R., Rodriguez J.M. Characterization of Staphylococcus aureus strains involved in human and bovine mastitis // FEMS immunological and medical microbiology. 2011. V. 62. Pp. 225-235.
7. Fernández L., Arroyo R., Espinosa I., Marín M, Jiménez E., Rodríguez J.M. Probiotics for human lactational mastitis // Benef. Microb. 2014. V. 5. Pp. 169-183.
8. Indrio F., Neu J. The intestinal microbiome of infants and the use of probiotics // Cur. Opin. Pediatr. 2011. V. 23. No. 2. Pp. 145-150.
9. Jost T., Lacroix C., Braegger C., Rochat F., Chassart C. Vertical mother-neonate transfer of maternal gut bacteria via breast-feeding // Environmental Microbiology. 2013. doi:10.1111/1462-2920.12238.
10. Lowy F.D. Staphulococcus aureus infections // N. Engl. J. Med. 1998. V. 339. Pp. 520-532.
11. Lehri B., Seddon A., Karlyshev A. Potential probiotic-associated traits revealed from completed high quality genome sequence of Lacobacillus fermentum 3872 // Standards in Genomic Sciences. 2017. doi:10.1186/s40793-017-0228-4.
12. Lehri B., Seddon A., Karlyshev A. Lactobacillus fermentum 3872 genome sequencing reveals plasmid and chromosomal genes potentially involved in a probiotic activity // FEMS Microbiol. Let. 2015. V. 362. Pp. 1-5.
13. Martin V., Maldonado A., Moles L., et al. Sharing of bacterial strains between breast milk and infant feces // J. of Human Lactation. 2012. V. 28. Pp. 36-44.
14. Ramiah K., van Reenen C., Dicks L. Surface-bound proteins of Lactobacillus plantarum 423 that contribute to adhesion of Caco-2 cells and their role in competitive exclusion and displacement of Clostridium sporogenes and Enterococcus faecalis // Res. Microbiol. 2008. V. 6. Pp. 470-475.
15. Saiman L., Okeefe M., Graham P., Wu F., et al. Hospital transmission of community-acquired methicillin-resistant Staphylococcus aureus among postpartum women // Clin. Infect. Dis. 2003. V. 37. Pp. 1313-19.
16. Schoenfelder S.M., Lange С., Eckart M., Hennig S., Kozytska S., Ziebuhr W. Successthrough diversity - how Staphylococcus epidermidis establishes as a nosocomial pathogen // Int. J. of Medical Microbiology. 2010. V. 300. Pp. 380-386.
17. Sears P.M., McCarthy K.K. Diagnosis of mastitis for therapy decisions // Veterinary Clinics of North America: Food Animal Practice. 2003. V. 19. Pp. 93-108.
18. Soto A., Martín V., Jiménez E., Mader I., Rodríguez J.M., Fernández L. Lactobacilli and bifidobacteria in human breast milk: influence of antibiotherapy and other host and clinical factors // J. Pediatr. Gastroenterol. Nutr. 2014. V. 59. Pp. 78-88.
19. Westerlund B., Korhonen T. Bacterial proteins binding to the mammalian extracellular matrics // Mol. Microbiol. 1993. V. 9. Pp. 687-694.
20. World Health Organization. Mastitis: causes and management. - Geneva: WHO, 2000.
21. Rukovodstvo po provedeniyu doklinicheskih issledovanij lekarstvennyh sredstv (immunobiologicheskie lekarstvennye preparaty). Ch. 2 [Guidelines for conducting preclinical studies of drugs (immunobiological drugs). Part 2]. Ed. by A.N. Mironov. Moscow: Grif i K. 2012. 536 p. (In Russian).
22. Brouillette E., Talbot B., Malouin F. The fibronectin-binding proteins of Staphulococcus aureus may promote mammary gland colonization in a lactating mouse model of Mastitis. Infect. Immun. 2003. V. 71. No. 4. Pp. 2292-2295.
23. Brouillette E., Martinez A., Boyll B., et al. Persistence of a Staphylococcus aureus Small-colony variant under antibiotic pressure in vivo. FEMS Immunol. and med. microbiol. 2004. V. 41. Issue 1. Pp. 35-41.
24. Delgado S., Arroyo R., Jiménez E., et al. Staphylococcus epidermidis strains isolated from breast milk of women suffering infectious mastitis: potential virulence traits and resistance to antibiotics. BMC Microbiol. 2009. V. 9. Pp. 82-85.
25. Delgado S., Arroyo R., Jiménez E., et al. Infectious mastitis during lactation: an underrated condition (I). Acta Pediatrica Espanola. 2009. V. 67. Pp. 77-84.
26. Delgado S., Garcia P., Fernandez L., Jimenez E., Rodriguez-Banos M., Del Campo R., Rodriguez J.M. Characterization of Staphylococcus aureus strains involved in human and bovine mastitis. FEMS immunological and medical microbiology. 2011. V. 62. Pp. 225-235.
27. Fernández L., Arroyo R., Espinosa I., Marín M, Jiménez E., Rodríguez J.M. Probiotics for human lactational mastitis. Benef. Microb. 2014. V. 5. Pp. 169-183.
28. Indrio F., Neu J. The intestinal microbiome of infants and the use of probiotics. Cur. Opin. Pediatr. 2011. V. 23. No. 2. Pp. 145-150.
29. Jost T., Lacroix C., Braegger C., Rochat F., Chassart C. Vertical mother-neonate transfer of maternal gut bacteria via breast-feeding. Environmental Microbiology. 2013. doi:10.1111/1462-2920.12238.
30. Lowy F.D. Staphulococcus aureus infections. N. Engl. J. Med. 1998. V. 339. Pp. 520-532.
31. Lehri B., Seddon A., Karlyshev A. Potential probiotic-associated traits revealed from completed high quality genome sequence of Lacobacillus fermentum 3872. Standards in Genomic Sciences. 2017. doi:10.1186/s40793-017-0228-4.
32. Lehri B., Seddon A., Karlyshev A. Lactobacillus fermentum 3872 genome sequencing reveals plasmid and chromosomal genes potentially involved in a probiotic activity. FEMS Microbiol. Let. 2015. V. 362. Pp. 1-5.
33. Martin V., Maldonado A., Moles L., et al. Sharing of bacterial strains between breast milk and infant feces. J. of Human Lactation. 2012. V. 28. Pp. 36-44.
34. Ramiah K., van Reenen C., Dicks L. Surface-bound proteins of Lactobacillus plantarum 423 that contribute to adhesion of Caco-2 cells and their role in competitive exclusion and displacement of Clostridium sporogenes and Enterococcus faecalis. Res. Microbiol. 2008. V. 6. Pp. 470-475.
35. Saiman L., Okeefe M., Graham P., Wu F., et al. Hospital transmission of community-acquired methicillin-resistant Staphylococcus aureus among postpartum women. Clin. Infect. Dis. 2003. V. 37. Pp. 1313-19.
36. Schoenfelder S.M., Lange С., Eckart M., Hennig S., Kozytska S., Ziebuhr W. Successthrough diversity - how Staphylococcus epidermidis establishes as a nosocomial pathogen. Int. J. of Medical Microbiology. 2010. V. 300. Pp. 380-386.
37. Sears P.M., McCarthy K.K. Diagnosis of mastitis for therapy decisions. Veterinary Clinics of North America: Food Animal Practice. 2003. V. 19. Pp. 93-108.
38. Soto A., Martín V., Jiménez E., Mader I., Rodríguez J.M., Fernández L. Lactobacilli and bifidobacteria in human breast milk: influence of antibiotherapy and other host and clinical factors. J. Pediatr. Gastroenterol. Nutr. 2014. V. 59. Pp. 78-88.
39. Westerlund B., Korhonen T. Bacterial proteins binding to the mammalian extracellular matrics. Mol. Microbiol. 1993. V. 9. Pp. 687-694.
40. World Health Organization. Mastitis: causes and management. Geneva: WHO, 2000.
Рецензия
Для цитирования:
Абрамов В.М., Хлебников В.С., Косарев И.В., Припутневич Т.В., Любасовская Л.А., Василенко Р.Н., Сакулин В.К., Каркищенко В.Н., Каркищенко Н.Н., Пчелинцев С.Ю., Карлышев А.В., Самойленко В.А., Мачулин А.В. Антагонистическая активность консорциума штаммов Lactobacillusfermentum ВКМ В-2793D и Lactobacillusreuteri ВКМ В-3144D, выделенных из женского молока, к мастит-индуцирующим патогенам. БИОМЕДИЦИНА. 2018;(3):46-54.
For citation:
Abramov V.M., Khlebnikov V.S., Kosarev I.V., Priputnevich T.V., Lyubasovskaya L.A., Vasilenko R.N., Sakulin V.K., Karkischenko V.N., Karkischenko N.N., Pchelintsev S.Yu., Karlyshev A.V., Samojlenko V.A., Machulin A.V. Antagonistic activity of a consortium of strains Lactobacillus fermentum ВКМ В-2793D and Lactobacillus reuteri ВКМ В-3144D isolated from human milk to mastitis-inductioning pathogens. Journal Biomed. 2018;(3):46-54. (In Russ.)