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. 1972 Oct;112(1):576–584. doi: 10.1128/jb.112.1.576-584.1972

Transfer Among Erwinia spp. and Other Enterobacteria of Antibiotic Resistance Carried on R Factors

Arun K Chatterjee 1, Mortimer P Starr 1
PMCID: PMC251447  PMID: 4562410

Abstract

Antibiotic resistance carried on R factors was transferred by conjugation from Escherichia coli B/r and Shigella flexneri 1a to Erwinia spp. Tetracycline resistance (TetR) carried on R factor R100 drd-56 was transferred from E. coli B/r to strains of Erwinia amylovora, E. aroideae, E. atroseptica, E. chrysanthemi, E. cytolytica, E. dissolvens, E. herbicola, E. nigrifluens, and E. nimipressuralis, but not to strains of Erwinia carotovora, E. carnegieana, E. dieffenbachiae, E. oleraceae, and E. quercina. Multiple antibiotic resistance (chloramphenicol, streptomycin, tetracycline; ChlR-StrR-TetR) carried on R factor SR1 was transferred from a clinical isolate of S. flexneri 1a to strains of E. aroideae, E. chrysanthemi, E. herbicola, and E. nigrifluens, but not to strains of other Erwinia spp. The frequency of this transfer was low with receptive cultures of Erwinia spp. and E. coli (F strain). Antibiotic resistance in the exconjugants showed varying degrees of stability in the presence or absence of acridine orange, depending on the strain tested. The frequencies of segregation to drug susceptibility in the presence of acridine orange, though low, suggest that the elements exist as plasmids in the majority of the Erwinia exconjugants. Multiple antibiotic resistance (ChlR-StrR-TetR) was found to segregate into various resistance classes (ChlR-StrR, StrR-TetR, TetR, StrR, and none) in these exconjugants. The exconjugants of E. amylovora, E. herbicola, and E. nigrifluens, to which R100 drd-56 was transferred from E. coli B/r, were sensitive to the male (F)-specific phage M13. There was a positive correlation between the susceptibility of exconjugants to the F-specific phage M13 and their ability to transfer R100 drd-56 to the recipient cultures of Escherichia coli, Erwinia herbicola, Salmonella typhimurium, and Shigella dysenteriae. Exceptions were, however, noted with Erwinia dissolvens and E. nimipressuralis exconjugants harboring R100 drd-56; these exconjugants, although not susceptible to M13, transferred R100 drd-56 to the recipient cultures. The frequency of transfer of R100 drd-56 and the levels of resistance to tetracycline in Erwinia exconjugants were found to differ markedly depending upon the strain employed. Transfer of multiple antibiotic resistance (ChlR-StrR-TetR) from Erwinia exconjugants was not obtained in preliminary trials with an E. coli F strain as the recipient culture.

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Selected References

These references are in PubMed. This may not be the complete list of references from this article.

  1. Anderson E. S. The ecology of transferable drug resistance in the enterobacteria. Annu Rev Microbiol. 1968;22:131–180. doi: 10.1146/annurev.mi.22.100168.001023. [DOI] [PubMed] [Google Scholar]
  2. BRISOU J., TYSSET C., VACHER B. [Study of a strain of Erwinia (Erwinia salmonis nv. sp.) isolated from a common trout (Salmo fario L.)]. Ann Inst Pasteur (Paris) 1959 Aug;97:241–244. [PubMed] [Google Scholar]
  3. Chatterjee A. K., Starr M. P. Genetic transfer of episomic elements among Erwinia species and other enterobacteria: F'Lac+. J Bacteriol. 1972 Jul;111(1):169–176. doi: 10.1128/jb.111.1.169-176.1972. [DOI] [PMC free article] [PubMed] [Google Scholar]
  4. Cohen S. N., Miller C. A. Non-chromosomal antibiotic resistance in bacteria. 3. Isolation of the discrete transfer unit of the R-factor R1. Proc Natl Acad Sci U S A. 1970 Oct;67(2):510–516. doi: 10.1073/pnas.67.2.510. [DOI] [PMC free article] [PubMed] [Google Scholar]
  5. Datta N., Lawn A. M., Meynell E. The relationship of F type piliation and F phage sensitivity to drug resistance transfer in R+F- Escherichia coli K 12. J Gen Microbiol. 1966 Nov;45(2):365–376. doi: 10.1099/00221287-45-2-365. [DOI] [PubMed] [Google Scholar]
  6. Franklin T. J. Resistance of Escherichia coli to tetracyclines. Changes in permeability to tetracyclines in Escherichia coli bearing transferable resistance factors. Biochem J. 1967 Oct;105(1):371–378. doi: 10.1042/bj1050371. [DOI] [PMC free article] [PubMed] [Google Scholar]
  7. GINOZA H. S., MATNEY T. S. TRANSMISSION OF A RESISTANCE TRANSFER FACTOR FROM ESCHERICHIA COLI TO 2 SPECIES OF PASTEURELLA. J Bacteriol. 1963 May;85:1177–1178. doi: 10.1128/jb.85.5.1177-1178.1963. [DOI] [PMC free article] [PubMed] [Google Scholar]
  8. Gilardi G. L., Bottone E., Birnbaum M. Unusual fermentative, gram-negative bacilli isolated from clinical specimens. I. Characterization of Erwinia strains of the "lathyri-herbicola group". Appl Microbiol. 1970 Jul;20(1):151–155. doi: 10.1128/am.20.1.151-155.1970. [DOI] [PMC free article] [PubMed] [Google Scholar]
  9. Gilardi G. L., Bottone E. Erwinia and yellow-pigmented Enterobacter isolates from human sources. Antonie Van Leeuwenhoek. 1971;37(4):529–535. doi: 10.1007/BF02218523. [DOI] [PubMed] [Google Scholar]
  10. HARADA K., SUZUKI M., KAMEDA M., MITSUHASHI S. On the drug-resistance of enteric bacteria. 2) Transmission of the drug-resistance among Enterobacteriaceae. Jpn J Exp Med. 1960 Aug;30:289–299. [PubMed] [Google Scholar]
  11. Hoar D. I. Fertility regulation in F-like resistance transfer factors. J Bacteriol. 1970 Mar;101(3):916–920. doi: 10.1128/jb.101.3.916-920.1970. [DOI] [PMC free article] [PubMed] [Google Scholar]
  12. KUWABARA S., AKIBA T., KOYAMA K., ARAI T. TRANSMISSION OF MULTIPLE DRUG-RESISTANCE FROM SHIGELLA FLEXNERI TO VIBRIO COMMA THROUGH CONJUGATION. Jpn J Microbiol. 1963 Aug;7:61–67. doi: 10.1111/j.1348-0421.1963.tb00243.x. [DOI] [PubMed] [Google Scholar]
  13. Kasamatsu H., Rownd R. Replication of R-factors in Proteus mirabilis: replication under relaxed control. J Mol Biol. 1970 Aug;51(3):473–489. doi: 10.1016/0022-2836(70)90002-1. [DOI] [PubMed] [Google Scholar]
  14. Lakso J. U., Starr M. P. Comparative injuriousness to plants of Erwinia spp. and other enterobacteria from plants and animals. J Appl Bacteriol. 1970 Dec;33(4):692–707. doi: 10.1111/j.1365-2672.1970.tb02252.x. [DOI] [PubMed] [Google Scholar]
  15. MURASCHI T. F., FRIEND M., BOLLES D. ERWINIA-LIKE MICROORGANISMS ISOLATED FROM ANIMAL AND HUMAN HOSTS. Appl Microbiol. 1965 Mar;13:128–131. doi: 10.1128/am.13.2.128-131.1965. [DOI] [PMC free article] [PubMed] [Google Scholar]
  16. Meynell E., Meynell G. G., Datta N. Phylogenetic relationships of drug-resistance factors and other transmissible bacterial plasmids. Bacteriol Rev. 1968 Mar;32(1):55–83. doi: 10.1128/br.32.1.55-83.1968. [DOI] [PMC free article] [PubMed] [Google Scholar]
  17. Novick R. P. Extrachromosomal inheritance in bacteria. Bacteriol Rev. 1969 Jun;33(2):210–263. doi: 10.1128/br.33.2.210-263.1969. [DOI] [PMC free article] [PubMed] [Google Scholar]
  18. Punch J. D., Kopecko D. J. Positive and negative control of R-factor replication in Proteus mirabilis. J Bacteriol. 1972 Jan;109(1):336–349. doi: 10.1128/jb.109.1.336-349.1972. [DOI] [PMC free article] [PubMed] [Google Scholar]
  19. Rownd R. Replication of a bacterial episome under relaxed control. J Mol Biol. 1969 Sep 28;44(3):387–402. doi: 10.1016/0022-2836(69)90368-4. [DOI] [PubMed] [Google Scholar]
  20. STARR M. P., MANDEL M. The nutrition of phytopathogenic bacteria. IV. Minimal nutritive requirements of the genus Erwinia. J Bacteriol. 1950 Nov;60(5):669–672. doi: 10.1128/jb.60.5.669-672.1950. [DOI] [PMC free article] [PubMed] [Google Scholar]
  21. Slotnick I. J., Tulman L. A human infection caused by an Erwinia species. Am J Med. 1967 Jul;43(1):147–150. doi: 10.1016/0002-9343(67)90157-x. [DOI] [PubMed] [Google Scholar]
  22. Starr M. P., Chatterjee A. K. The genus Erwinia: enterobacteria pathogenic to plants and animals. Annu Rev Microbiol. 1972;26:389–426. doi: 10.1146/annurev.mi.26.100172.002133. [DOI] [PubMed] [Google Scholar]
  23. Starr M. P., Mandel M. DNA base composition and taxonomy of phyopathogenic and other enterobacteria. J Gen Microbiol. 1969 Apr;56(1):113–123. doi: 10.1099/00221287-56-1-113. [DOI] [PubMed] [Google Scholar]
  24. Von Graevenitz A. Erwinia species isolates. Ann N Y Acad Sci. 1970 Oct 30;174(2):436–443. doi: 10.1111/j.1749-6632.1970.tb45571.x. [DOI] [PubMed] [Google Scholar]
  25. Von Graevenitz A. Recognition and differential diagnosis of Erwinia herbicola strains isolated in the hospital. Pathol Microbiol (Basel) 1971;37(1):84–88. doi: 10.1159/000162308. [DOI] [PubMed] [Google Scholar]
  26. Von Graevenitz A., Strouse A. Isolation of Erwinia spp. from human sources. Antonie Van Leeuwenhoek. 1966;32(4):429–430. doi: 10.1007/BF02097494. [DOI] [PubMed] [Google Scholar]
  27. WATANABE T., FUKASAWA T. Episome-mediated transfer of drug resistance in Enterobacteriaceae IV. Interactions between resistance transfer factor and F-factor in Escherichia coli K-12. J Bacteriol. 1962 Apr;83:727–735. doi: 10.1128/jb.83.4.727-735.1962. [DOI] [PMC free article] [PubMed] [Google Scholar]
  28. WATANABE T., FUKASAWA T. Episome-mediated transfer of drug resistance in Enterobacteriaceae. I. Transfer of resistance factors by conjugation. J Bacteriol. 1961 May;81:669–678. doi: 10.1128/jb.81.5.669-678.1961. [DOI] [PMC free article] [PubMed] [Google Scholar]
  29. WATANABE T., NISHIDA H., OGATA C., ARAI T., SATO S. EPISOME-MEDIATED TRANSFER OF DRUG RESISTANCE IN ENTEROBACTERIACEAE. VII. TWO TYPES OF NATURALLY OCCURRING R FACTORS. J Bacteriol. 1964 Sep;88:716–726. doi: 10.1128/jb.88.3.716-726.1964. [DOI] [PMC free article] [PubMed] [Google Scholar]
  30. Watanabe T. Evolutionary relationships of R factors with other episomes and plasmids. Fed Proc. 1967 Jan-Feb;26(1):23–28. [PubMed] [Google Scholar]
  31. Wechsler A., Bottone E., Lasser R., Korenman G. Brain abscess caused by an Erwinia species. Report of a case and review of the literature. Am J Med. 1971 Nov;51(5):680–684. doi: 10.1016/0002-9343(71)90294-4. [DOI] [PubMed] [Google Scholar]
  32. White J. N., Starr M. P. Glucose fermentation endproducts of Erwinia spp. and other enterobacteria. J Appl Bacteriol. 1971 Jun;34(2):459–475. doi: 10.1111/j.1365-2672.1971.tb02306.x. [DOI] [PubMed] [Google Scholar]

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