Skip to main content
Bulletin of the New York Academy of Medicine logoLink to Bulletin of the New York Academy of Medicine
. 1987 Apr;63(3):237–252.

Virulence versus resistance.

K M Krasinski
PMCID: PMC1629237  PMID: 3300826

Full text

PDF
237

Selected References

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

  1. Angus B. L., Carey A. M., Caron D. A., Kropinski A. M., Hancock R. E. Outer membrane permeability in Pseudomonas aeruginosa: comparison of a wild-type with an antibiotic-supersusceptible mutant. Antimicrob Agents Chemother. 1982 Feb;21(2):299–309. doi: 10.1128/aac.21.2.299. [DOI] [PMC free article] [PubMed] [Google Scholar]
  2. Beachey E. H., Ofek I. Epithelial cell binding of group A streptococci by lipoteichoic acid on fimbriae denuded of M protein. J Exp Med. 1976 Apr 1;143(4):759–771. doi: 10.1084/jem.143.4.759. [DOI] [PMC free article] [PubMed] [Google Scholar]
  3. Cannon J. G., Sparling P. F. The genetics of the gonococcus. Annu Rev Microbiol. 1984;38:111–133. doi: 10.1146/annurev.mi.38.100184.000551. [DOI] [PubMed] [Google Scholar]
  4. Clark R. B., Janda J. M., Bottone E. J. Phenotypic factors correlated with the absence of virulence among gentamicin-resistant Pseudomonas aeruginosa strains. J Clin Microbiol. 1984 Aug;20(2):235–238. doi: 10.1128/jcm.20.2.235-238.1984. [DOI] [PMC free article] [PubMed] [Google Scholar]
  5. Comstock G. W. Epidemiology of tuberculosis. Am Rev Respir Dis. 1982 Mar;125(3 Pt 2):8–15. doi: 10.1164/arrd.1982.125.3P2.8. [DOI] [PubMed] [Google Scholar]
  6. Daddi G., Lucchesi M., Zubiani M. Some remarks on the recent bacteriological research on tuberculosis. Indian J Chest Dis Allied Sci. 1982 Apr-Sep;24(2-3):164–169. [PubMed] [Google Scholar]
  7. Daly J. A., Lee T. J., Spitznagel J. K., Sparling P. F. Gonococci with mutations to low-level penicillin resistance exhibit increased sensitivity to the oxygen-independent bactericidal activity of human polymorphonuclear leukocyte granule extracts. Infect Immun. 1982 Mar;35(3):826–833. doi: 10.1128/iai.35.3.826-833.1982. [DOI] [PMC free article] [PubMed] [Google Scholar]
  8. Draper D. L., James J. F., Brooks G. F., Sweet R. L. Comparison of virulence markers of peritoneal and fallopian tube isolates with endocervical Neisseria gonorrhoeae isolates from women with acute salpingitis. Infect Immun. 1980 Mar;27(3):882–888. doi: 10.1128/iai.27.3.882-888.1980. [DOI] [PMC free article] [PubMed] [Google Scholar]
  9. DuPont H. L., Hornick R. B., Dawkins A. T., Snyder M. J., Formal S. B. The response of man to virulent Shigella flexneri 2a. J Infect Dis. 1969 Mar;119(3):296–299. doi: 10.1093/infdis/119.3.296. [DOI] [PubMed] [Google Scholar]
  10. Eisenstein B. I., Lee T. J., Sparling P. F. Penicillin sensitivity and serum resistance are independent attributes of strains of Neisseria gonorrhoeae causing disseminated gonococcal infection. Infect Immun. 1977 Mar;15(3):834–841. doi: 10.1128/iai.15.3.834-841.1977. [DOI] [PMC free article] [PubMed] [Google Scholar]
  11. Eisenstein B. I., Sparling P. F. Mutations to increased antibiotic sensitivity in naturally-occurring gonococci. Nature. 1978 Jan 19;271(5642):242–244. doi: 10.1038/271242a0. [DOI] [PubMed] [Google Scholar]
  12. Fairshter R. D., Randazzo G. P., Garlin J., Wilson A. F. Failure of isoniazid prophylaxis after exposure to isoniazid-resistant tuberculosis. Am Rev Respir Dis. 1975 Jul;112(1):37–42. doi: 10.1164/arrd.1975.112.1.37. [DOI] [PubMed] [Google Scholar]
  13. Faruki H., Kohmescher R. N., McKinney W. P., Sparling P. F. A community-based outbreak of infection with penicillin-resistant Neisseria gonorrhoeae not producing penicillinase (chromosomally mediated resistance). N Engl J Med. 1985 Sep 5;313(10):607–611. doi: 10.1056/NEJM198509053131004. [DOI] [PubMed] [Google Scholar]
  14. Formal S. B., Hornick R. B. Invasive Escherichia coli. J Infect Dis. 1978 May;137(5):641–644. doi: 10.1093/infdis/137.5.641. [DOI] [PubMed] [Google Scholar]
  15. GORDON J. E., ASCOLI W., PIERCE V., GUZMAN M. A., MATA L. J. STUDIES OF DIARRHEAL DISEASE IN CENTRAL AMERICA. VI. AN EPIDEMIC OF DIARRHEA IN A GUATEMALAN HIGHLAND VILLAGE, WITH A COMPONENT DUE TO SHIGELLA DYSENTERIAE, TYPE 1. Am J Trop Med Hyg. 1965 May;14:404–411. [PubMed] [Google Scholar]
  16. Gangarosa E. J., Bennett J. V., Wyatt C., Pierce P. E., Olarte J., Hernandes P. M., Vázquez V., Bessudo D. An epidemic-associated episome? J Infect Dis. 1972 Aug;126(2):215–218. doi: 10.1093/infdis/126.2.215. [DOI] [PubMed] [Google Scholar]
  17. Greene W. H., Moody M., Schimpff S., Young V. M., Wiernik P. H. Pseudomonas aeruginosa resistant to carbenicillin and gentamicin. Epidemiologic and clinical aspects in a cancer center. Ann Intern Med. 1973 Nov;79(5):684–689. doi: 10.7326/0003-4819-79-5-684. [DOI] [PubMed] [Google Scholar]
  18. Gutmann L., Williamson R., Moreau N., Kitzis M. D., Collatz E., Acar J. F., Goldstein F. W. Cross-resistance to nalidixic acid, trimethoprim, and chloramphenicol associated with alterations in outer membrane proteins of Klebsiella, Enterobacter, and Serratia. J Infect Dis. 1985 Mar;151(3):501–507. doi: 10.1093/infdis/151.3.501. [DOI] [PubMed] [Google Scholar]
  19. Hadfield T. L., Monson M. H., Wachsmuth I. K. An outbreak of antibiotic-resistant Salmonella enteritidis in Liberia, West Africa. J Infect Dis. 1985 May;151(5):790–795. doi: 10.1093/infdis/151.5.790. [DOI] [PubMed] [Google Scholar]
  20. Haltalin K. C., Woodman E., Nelson J. D. Colicin types of Shigella sonnei in relation to antibiotic resistance. J Infect Dis. 1975 Sep;132(3):307–315. doi: 10.1093/infdis/132.3.307. [DOI] [PubMed] [Google Scholar]
  21. Hildebrandt J. F., Mayer L. W., Wang S. P., Buchanan T. M. Neisseria gonorrhoeae acquire a new principal outer-membrane protein when transformed to resistance to serum bactericidal activity. Infect Immun. 1978 Apr;20(1):267–272. doi: 10.1128/iai.20.1.267-272.1978. [DOI] [PMC free article] [PubMed] [Google Scholar]
  22. Keys T. F., Washington J. A., 2nd Gentamicin-resistant Pseudomonas aeruginosa: Mayo Clinic Experience, 1970-1976. Mayo Clin Proc. 1977 Dec;52(12):797–801. [PubMed] [Google Scholar]
  23. Khakoo R. A., Kluge R. M. Decreased virulence of gentamicin-resistant strains of Pseudomonas aeruginosa in a rat model. J Lab Clin Med. 1978 Jan;91(1):96–103. [PubMed] [Google Scholar]
  24. MIDDLEBROOK G., COHN M. L. Some observations on the pathogenicity of isoniazid-resistant variants of tubercle bacilli. Science. 1953 Sep 11;118(3063):297–299. doi: 10.1126/science.118.3063.297. [DOI] [PubMed] [Google Scholar]
  25. MITCHISON D. A. Tubercle bacilli resistant to isoniazid; virulence and response to treatment with isoniazid in guinea-pigs. Br Med J. 1954 Jan 16;1(4854):128–130. doi: 10.1136/bmj.1.4854.128. [DOI] [PMC free article] [PubMed] [Google Scholar]
  26. Marsik F. J., Parisi J. T. Significance of Staphylococcus epidermidis in the clinical laboratory. Appl Microbiol. 1973 Jan;25(1):11–14. doi: 10.1128/am.25.1.11-14.1973. [DOI] [PMC free article] [PubMed] [Google Scholar]
  27. Mata L. J., Gangarosa E. J., Cáceres A., Perera D. R., Mejicanos M. L. Epidemic Shiga bacillus dysentery in Central America. I. Etiologic investigations in Guatemala, 1969. J Infect Dis. 1970 Sep;122(3):170–180. doi: 10.1093/infdis/122.3.170. [DOI] [PubMed] [Google Scholar]
  28. McConnell M. M., Willshaw G. A., Smith H. R., Scotland S. M., Rowe B. Transposition of ampicillin resistance to an enterotoxin plasmid in an Escherichia coli strain of human origin. J Bacteriol. 1979 Aug;139(2):346–355. doi: 10.1128/jb.139.2.346-355.1979. [DOI] [PMC free article] [PubMed] [Google Scholar]
  29. Mendizábal-Morris C. A., Mata L. J., Gangarosa E. J., Guzmán G. Epidemic Shiga-bacillus dysentery in Central America. Derivation of the epidemic and its progression in Guatemala, 1968-69. Am J Trop Med Hyg. 1971 Nov;20(6):927–933. doi: 10.4269/ajtmh.1971.20.927. [DOI] [PubMed] [Google Scholar]
  30. Meyer R. D., Lewis R. P., Halter J., White M. Gentamicin-resistant Pseudomonas aeruginosa and Serratia marcescens in a general hospital. Lancet. 1976 Mar 13;1(7959):580–583. doi: 10.1016/s0140-6736(76)90370-6. [DOI] [PubMed] [Google Scholar]
  31. Murray B. E., Levine M. M., Cordano A. M., D'Ottone K., Jayanetra P., Kopecko D., Pan-Urae R., Prenzel I. Survey of plasmids in Salmonella typhi from Chile and Thailand. J Infect Dis. 1985 Mar;151(3):551–555. doi: 10.1093/infdis/151.3.551. [DOI] [PubMed] [Google Scholar]
  32. Olsen G. A., Lomholt G. Gonorrhoea treated by a combination of probenecid and sodium penicillin G. Br J Vener Dis. 1969 Jun;45(2):144–148. doi: 10.1136/sti.45.2.144. [DOI] [PMC free article] [PubMed] [Google Scholar]
  33. Peterson P. K., Quie P. G. Bacterial surface components and the pathogenesis of infectious diseases. Annu Rev Med. 1981;32:29–43. doi: 10.1146/annurev.me.32.020181.000333. [DOI] [PubMed] [Google Scholar]
  34. Plaut A. G. Microbial IgA proteases. N Engl J Med. 1978 Jun 29;298(26):1459–1463. doi: 10.1056/NEJM197806292982608. [DOI] [PubMed] [Google Scholar]
  35. Ramirez-Ronda C. H. Adherence of glucan-positive and glucan-negative streptococcal strains to normal and damaged heart valves. J Clin Invest. 1978 Oct;62(4):805–814. doi: 10.1172/JCI109192. [DOI] [PMC free article] [PubMed] [Google Scholar]
  36. Reller L. B., Rivas E. N., Masferrer R., Bloch M., Gangarosa E. J. Epidemic shiga-bacillus dysentery in Central America. Evolution of the outbreak in El Salvador, 1969-70. Am J Trop Med Hyg. 1971 Nov;20(6):934–940. doi: 10.4269/ajtmh.1971.20.934. [DOI] [PubMed] [Google Scholar]
  37. Sack D. A., Kaminsky D. C., Sack R. B., Wamola I. A., Orskov F., Orskov I., Slack R. C., Arthur R. R., Kapikian A. Z. Enterotoxigenic Escherichia coli diarrhea of travelers: a prospective study of American Peace Corps volunteers. Johns Hopkins Med J. 1977 Aug;141(2):63–70. [PubMed] [Google Scholar]
  38. Sander G. Colicin E3 treatment renders ribosomes more resistant to streptomycin and reduces miscoding. FEBS Lett. 1979 Jan 15;97(2):217–220. doi: 10.1016/0014-5793(79)80087-3. [DOI] [PubMed] [Google Scholar]
  39. Sanders C. C., Sanders W. E., Jr Microbial resistance to newer generation beta-lactam antibiotics: clinical and laboratory implications. J Infect Dis. 1985 Mar;151(3):399–406. doi: 10.1093/infdis/151.3.399. [DOI] [PubMed] [Google Scholar]
  40. Santos D. S., Palchaudhuri S., Maas W. K. Genetic and physical characteristics of an enterotoxin plasmid. J Bacteriol. 1975 Dec;124(3):1240–1247. doi: 10.1128/jb.124.3.1240-1247.1975. [DOI] [PMC free article] [PubMed] [Google Scholar]
  41. Shearer B. G., Legakis N. J. Pseudomonas aeruginosa: evidence for the involvement of lipopolysaccharide in determining outer membrane permeability to carbenicillin and gentamicin. J Infect Dis. 1985 Aug;152(2):351–355. doi: 10.1093/infdis/152.2.351. [DOI] [PubMed] [Google Scholar]
  42. Smith H. W. Is it safe to use Escherichia coli K12 in recombinant DNA experiments? J Infect Dis. 1978 May;137(5):655–660. doi: 10.1093/infdis/137.5.655. [DOI] [PubMed] [Google Scholar]
  43. Smith H. W., Linggood M. A. Observations on the pathogenic properties of the K88, Hly and Ent plasmids of Escherichia coli with particular reference to porcine diarrhoea. J Med Microbiol. 1971 Nov;4(4):467–485. doi: 10.1099/00222615-4-4-467. [DOI] [PubMed] [Google Scholar]
  44. Snider D. E., Jr, Kelly G. D., Cauthen G. M., Thompson N. J., Kilburn J. O. Infection and disease among contacts of tuberculosis cases with drug-resistant and drug-susceptible bacilli. Am Rev Respir Dis. 1985 Jul;132(1):125–132. doi: 10.1164/arrd.1985.132.1.125. [DOI] [PubMed] [Google Scholar]
  45. So M., Boyer H. W., Betlach M., Falkow S. Molecular cloning of an Escherichia coli plasmid determinant than encodes for the production of heat-stable enterotoxin. J Bacteriol. 1976 Oct;128(1):463–472. doi: 10.1128/jb.128.1.463-472.1976. [DOI] [PMC free article] [PubMed] [Google Scholar]
  46. So M., Heffron F., Falkow S. Method for the genetic labeling of cryptic plasmids. J Bacteriol. 1978 Mar;133(3):1520–1523. doi: 10.1128/jb.133.3.1520-1523.1978. [DOI] [PMC free article] [PubMed] [Google Scholar]
  47. Staat R. H., Langley S. D., Doyle R. J. Streptococcus mutans adherence: presumptive evidence for protein-mediated attachment followed by glucan-dependent cellular accumulation. Infect Immun. 1980 Feb;27(2):675–681. doi: 10.1128/iai.27.2.675-681.1980. [DOI] [PMC free article] [PubMed] [Google Scholar]
  48. Swanson J. Studies on gonococcus infection. IV. Pili: their role in attachment of gonococci to tissue culture cells. J Exp Med. 1973 Mar 1;137(3):571–589. doi: 10.1084/jem.137.3.571. [DOI] [PMC free article] [PubMed] [Google Scholar]
  49. Swim S. C., Gfell M. A., Wilde C. E., 3rd, Rosenthal R. S. Strain distribution in extents of lysozyme resistance and O-acetylation of gonococcal peptidoglycan determined by high-performance liquid chromatography. Infect Immun. 1983 Nov;42(2):446–452. doi: 10.1128/iai.42.2.446-452.1983. [DOI] [PMC free article] [PubMed] [Google Scholar]
  50. Taylor P. W., Hughes C. Plasmid carriage and the serum sensitivity of enterobacteria. Infect Immun. 1978 Oct;22(1):10–17. doi: 10.1128/iai.22.1.10-17.1978. [DOI] [PMC free article] [PubMed] [Google Scholar]
  51. Thorne G. M., Farrar W. E., Jr Genetic properties of R factors associated with epidemic strains of Shigella dysenteriae type I from Central America and Salmonella typhi from Mexico. J Infect Dis. 1973 Jul;128(1):132–136. doi: 10.1093/infdis/128.1.132. [DOI] [PubMed] [Google Scholar]
  52. Thorne G. M., Farrar W. E., Jr Superinfection compatibility of R factors in Shigella dysenteriae type 1 from Central America and Salmonella typhi from Mexico. J Infect Dis. 1974 Sep;130(3):284–287. doi: 10.1093/infdis/130.3.284. [DOI] [PubMed] [Google Scholar]
  53. Vicente A. C., de Almeida D. F. Identification of multiple-resistance (R) and colicinogeny (Col) plasmids in an epidemic Salmonella agona serotype in Rio de Janeiro. J Hyg (Lond) 1984 Aug;93(1):79–84. doi: 10.1017/s0022172400060952. [DOI] [PMC free article] [PubMed] [Google Scholar]
  54. Wiesner P. J., Handsfield H. H., Holmes K. K. Low antibiotic resistance of gonococci causing disseminated infection. N Engl J Med. 1973 Jun 7;288(23):1221–1222. doi: 10.1056/NEJM197306072882308. [DOI] [PubMed] [Google Scholar]
  55. Wilkinson B. J., Sisson S. P., Kim Y., Peterson P. K. Localization of the third component of complement on the cell wall of encapsulated Staphylococcus aureus M: implications for the mechanism of resistance to phagocytosis. Infect Immun. 1979 Dec;26(3):1159–1163. doi: 10.1128/iai.26.3.1159-1163.1979. [DOI] [PMC free article] [PubMed] [Google Scholar]

Articles from Bulletin of the New York Academy of Medicine are provided here courtesy of New York Academy of Medicine

RESOURCES