Email updates

Keep up to date with the latest news and content from BMC Infectious Diseases and BioMed Central.

Open Access Research article

Clustering of antibiotic resistance of E. coli in couples: suggestion for a major role of conjugal transmission

Susanne Lietzau1, Elke Raum12, Heike von Baum3, Reinhard Marre3 and Hermann Brenner12*

Author Affiliations

1 Department of Epidemiology, German Centre for Research on Ageing, Heidelberg, Germany

2 Division of Clinical Epidemiology and Aging Research, German Cancer Research Center, Heidelberg, Germany

3 Department of Medical Microbiology and Hygiene, University of Ulm, Ulm, Germany

For all author emails, please log on.

BMC Infectious Diseases 2006, 6:119  doi:10.1186/1471-2334-6-119


The electronic version of this article is the complete one and can be found online at: http://www.biomedcentral.com/1471-2334/6/119


Received:21 November 2005
Accepted:18 July 2006
Published:18 July 2006

© 2006 Lietzau et al; licensee BioMed Central Ltd.

This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

Abstract

Background

Spread of antibiotic resistance in hospitals is a well-known problem, but studies investigating the importance of factors potentially related to the spread of resistant bacteria in outpatients are sparse.

Methods

Stool samples were obtained from 206 healthy couples in a community setting in Southern Germany in 2002–2003. E. coli was cultured and minimal inhibition concentrations were tested. Prevalences of E. coli resistance to commonly prescribed antibiotics according to potential risk factors were ascertained.

Results

Prevalences of ampicillin resistance were 15.7% and 19.4% for women and men, respectively. About ten percent and 15% of all isolates were resistant to cotrimoxazole and doxycycline, respectively. A partner carrying resistance was the main risk factor for being colonized with resistant E. coli. Odds ratios (95% CI) for ampicillin and cotrimoxazole resistance given carriage of resistant isolates by the partner were 6.9 (3.1–15.5) and 3.3 (1.5–18.0), respectively.

Conclusion

Our data suggest that conjugal transmission may be more important for the spread of antibiotic resistance in the community setting than commonly suspected risk factors such as previous antibiotic intake or hospital contacts.

Background

There is worldwide concern about the appearance and the rise of bacterial resistance to commonly used antibiotics [1,2]. Although the great majority of antibiotics are prescribed outside the hospitals and the human gut represents a large reservoir for potentially transferable antibiotic resistant E. coli, the potential role of transmission of antibiotic resistant bacteria between healthy individuals in the community is almost unexplored. We aimed to investigate the potential role of conjugal transmission of resistant E. coli compared to other suggested risk factors of carriage of resistant E. coli, like recent antibiotic intake or hospital stay, in a large community-based study.

Methods

Study population and data collection

This analysis was carried out as part of a large scale study primarily designed to investigate risk factors of carriage of antibiotic resistant E. coli in outpatient toddlers in Ulm, a city in Southern Germany. From July 2002 to July 2003 during the visit of a cooperating pediatrician, the accompanying parent and later on their spouses at home were also asked to participate in this study. Sociodemographic and medical data for the men (further referred to as "index persons") and their wives were obtained with a self-administered standardized questionnaire. In addition, all couples were asked to collect stool samples at home and to send them by mail to the study laboratory at the Department of Medical Microbiology and Hygiene at the University of Ulm (response rates among mothers and fathers 88.4% and 87.8%, respectively), where E. coli was cultured and resistance testing was carried out (see below). The study was approved by the ethical committees of the medical faculty of the University of Heidelberg, and of the chamber of physicians of the state of Baden-Württemberg. In this analysis, all couples were included, who gave written informed consent, and of whom both partners sent a stool sample from which E. coli could be cultured.

E. coli culturing and antibiotic resistance testing

Stool samples were incubated on McConkey plates at 36 ± 1°C for 24 hours. Colonies of different phenotypes were tested with API20E (bioMérieux, France) in order to identify E. coli strains. Up to three phenotypically different E. coli colonies were kept frozen at -80°C in microbanks until susceptibility testing was performed. One of these colonies was randomly selected for resistance testing. Minimal inhibitory concentrations (MIC) were tested using micro well plates with various concentrations of antibiotics and an optical reader (Merlin, Germany) according to German national standards (DIN 58940) [3]. Weekly testing of E. coli strain ATCC 25922 was used for quality control. MICs for the following commonly employed antibiotics were determined (tested ranges and cutpoints of MIC in μg/ml are given in parentheses): ampicillin (1–128 μg/ml; >8), amoxicillin/clavulanic acid (1/2–128/2 μg/ml;>8/2), piperacillin/tazobactam (1/4–128/4 μg/ml;>32/4), cefpodoxime proxetil (0.25–32 μg/ml;>4), cefuroxime (1–128 μg/ml;>8), doxycycline (0.25–32 μg/ml;>4), gentamicin (0.25–32 μg/ml;>4), cotrimoxazole (2–28 μg/ml;>64), nalidixic acid (1–128 μg/ml;>32) and levofloxacin (0.0625–8 μg/ml;>2).

Statistical analyses

We used descriptive statistics to characterize the index persons and their partners with respect to various sociodemographic and life-style factors, and to assess the prevalence of resistance of E. coli strains to the various antibiotics.

Next, potential determinants of antibiotic resistance among the index persons were evaluated. These analyses were restricted to ampicillin, doxycycline and cotrimoxazole as the resistance prevalences were too low for other substances to carry out meaningful analyses of associations. Apart from the presence of a spouse with an ampicillin, doxycycline or cotrimoxazole resistant E. coli, respectively, the following factors were considered as possible determinants of antibiotic resistance in bivariate as well as multivariable analysis (multiple logistic regression): antibiotic use within last three months, hospital stay within last 12 months, hospital/nursing home visit within last 12 months and frequent (daily) meat consumption. The time intervals were chosen to be as short as possible, but broad enough to include minimum number of subjects to allow for meaningful statistical analyses.

All analyses were carried out with the statistical software package SAS, Version 8.2.

Results

In total, 206 couples were included in the analysis. Mean age of the index persons and their partners was 35 years (SD ± 5) and 32 years (SD ± 5), respectively. In total, 98% of the men were half- or full-time employed, whereas 72% of the spouses were housewives. Nine percent of the index persons and 12% of the partners had taken antibiotics within the last three months. A hospital stay within the last 12 months was reported by 6% and 26.6% of the index persons and their partners, and 58% and 62.1% had visited a hospital or nursing home during the last year, respectively. Sixty-one percent of the index person consumed meat daily, spouses reported daily meat consumption less often (51%).

The resistance prevalences of E. coli to various antibiotics were very similar among the men and their spouses. Among E. coli isolates cultured from stool of the index persons and their spouses, ampicillin resistance prevalences were 18.9% and 15.7%, respectively. Ten percent and 13.1% of the isolates from the index person and 9.2% and 14.9% of the isolates of their spouses carried cotrimoxazole and doxycycline resistance, respectively. Cephalosporine, gentamicin and quinolones resistance prevalences were three percent or less.

In bivariate analyses there were no indications that recent antibiotic intake, hospital stay or visit within the last 12 months or daily meat consumption were associated with antibiotic resistance (see table 1). Furthermore, no associations were found between antibiotic resistance and a variety of sociodemographic factors including the patients' age, education, occupation, number of family members in the household, square meter per person in the household, elderly persons in the household and a pet in the household (data not shown). By contrast, strong associations were found with antibiotic resistance among the partners. The associations for ampicillin resistant E. coli carried by both partners were highly significant. Resistance prevalences among the index persons were increased to 50.0%, 25.0% and 20.6% for ampicillin, cotrimoxazole and doxycycline, respectively, if the partner carried ampicillin, cotrimoxazole or doxycycline resistant E. coli, respectively, compared to resistance prevalences of 11.9%, 8.1% and 11.6%, respectively, observed otherwise.

Table 1. Bivariate analyses of the association of E. coli resistance to ampicillin, cotrimoxazole and doxycycline among the index persons.

Table 2 shows the results of the multivariable analysis. After adjusting for antibiotic use within the last three months, a hospital stay during the last 12 months, visit of a hospital or nursing home within the last 12 months and frequency of meat consumption, spouses with ampicillin, doxycycline or cotrimoxazole resistant E. coli remained the main risk factor for the index persons to be colonized with resistant E. coli. In particular, carriage of ampicillin resistant E. coli by the partner was strongly and significantly associated with E. coli resistance to ampicillin in the index person (OR: 6.9; 95% CI: 3.1–15.5). Also carriage of cotrimoxazole resistant E. coli by the partner was associated with a significantly increased risk for the index partner to carry E. coli with cotrimoxazole resistance (OR: 3.5; 95% CI: 1.5–11.1).

Table 2. Multivariable analysis of potential risk factors of E. coli resistance to ampicillin, cotrimoxazole and doxycycline among index persons and their spouse.

Discussion

The E. coli resistance prevalences in this community-based sample of couples from Southern Germany assessed in 2002–2003 were still on a relatively low level. The by far most important risk factor for the colonization with ampicillin, cotrimoxazole and doxycycline resistant E. coli was to live with a spouse carrying resistance to the respective antibiotic. Especially carriage of ampicillin resistant E. coli by the partner was significantly and strongly associated with ampicillin resistance in the index persons.

The resistance prevalences found in our study were similar to those found in a study conducted in the same region between May 1999 and January 2000 in Germany investigating E. coli resistance prevalences in the faeces of outpatients aged 40 years and older by the same methodology [4]. By contrast, much higher resistance prevalences in the community setting have been reported from studies conducted in the clinical sector in Germany, but direct comparisons are difficult due to selective sampling and different handling of the samples in the clinical setting.

Oral administration of antibiotics can influence the normal intestinal microflora and can lead to an overgrowth of resistant bacteria. But if the resistant bacteria persist for weeks or for months after the end of antibiotic treatment is discussed controversially [4-10]. Also hospital stay has previously been identified as potential risk factor for the carriage of resistant bacteria [11,12]. In our study, this factor did not play a major role. However, this finding may partly reflect lack of differentiation regarding important factors such as duration of stay, reason for admission or type of surgery. Furthermore meat consumption has been suggested as a potential sources of resistant bacteria and/or resistance genes [15], but in this study daily meat consumption was not associated with a higher risk for E. coli resistance. To our knowledge, our study was the first to address clustering of antibiotic resistant E. coli in a large sample of healthy couples from the community setting, and to assess the association of antibiotic resistant E. coli cultured from stool samples of the partner with own carriage of resistant E. coli strains.

Data on familial clustering of resistant bacteria in the outpatient setting are sparse. In a study from Sweden, stool samples were obtained from household members of outpatients with urinary tract infections [14]. In 16 (32%) samples of 51 family members trimethoprim resistance was found if trimethoprim resistant E. coli caused the urinary tract infection. Only one (2%) of 46 persons living in the same households carried trimethoprim resistant E. coli if the pathogen of the infection was sensitive to trimethoprim. Another study conducted in the United States in 1992 focused on the possible transmission of trimethoprim resistant E. coli from 33 day care center children to household members [15]. Family members of colonized children had significantly more resistant isolates than those from noncolonized children (26% vs. 2%). Although both studies included small numbers of families and were focused on trimethorprim resistance only and neither study explicitly addressed clustering between partners their findings are consistent with the suggestion strongly supported by our study that intrafamilial transmission is likely to play a major role in the spread of antibiotic resistance in the community setting.

Several limitations have to be kept in mind when interpreting our study results. The study was performed in 2002 to 2003 and therefore the resistance prevalences may not be as applicable to 2006. Furthermore the lack of associations of putative risk factors other than a partner with resistant E. coli must be interpreted with caution given the limited power of the study to address those associations. We relied on self-reports for our analyses regarding recent antibiotic intake, because not all antibiotics prescribed by the general practitioners are actually used and furthermore adults often receive antibiotic prescriptions from different physicians. Although self-reports of antibiotic intake may not always be reliable, major recall bias regarding antibiotic therapy within the last three months appears to be unlikely. However, our data and sample size limitations did not allow further stratification of previous antibiotic therapy by specific antibiotics, which may have diluted associations with resistance prevalences that might have been found for homologous substances.

In theory, clustering of antibiotic resistance in couples may reflect common sources of acquisition of resistant strains (or of resistant plasmids) as well as transmission of resistant strains (or resistant plasmids) between partners. Common sources of acquisition may be, for example, hospital visits or hospital stays of one partner (who might have frequent visits by the other partner), or common nutritional sources. Neither of these factors was found to play an important role in our study, however, which suggests that transmission is probably much more relevant in this sample.

Common sources of acquisition might also be other household members, such as children. Furthermore, potential transmission between partners may either be direct or indirect, e.g. via transmission from one partner to a child, who may then transmit resistant E. coli to the partner. Longitudinal studies will be needed for a definitive clarification of these potential alternative pathways, even though conjugal transmission appears to be the most plausible explanation for the observed patterns. However, the main finding of our study that couples are more frequently colonized with resistant E. coli, if their partner carries the same type of resistance, and that this factor is likely to be more important than other possible risk factors, e.g. recent antibiotic intake, holds regardless of the underlying mechanisms and pathway.

Conclusion

The prevalences of antibiotic resistant E. coli in this population of young couples in Germany were not yet on a threatening level. Even though we only isolated E. coli from stool samples, it is to assume that first-line therapies for E. coli related diseases, like cotrimoxazole for urinary tract infection, should have been effective in most cases at the time of the study (2002–2003), taking into account that a large proportion of urinary tract infections are caused by self-infection [16]. Carriage of E. coli resistance by the partner is likely to be a key factor for carrying resistant E. coli, and this risk factor appears to be more important than other suggested potential risk factors among young adults in the community setting.

Abbreviations

CI = confidence interval; E. coli = Escherichia coli; MIC = Minimal inhibitory concentrations; OR = Odds ratios; SD = Standard deviation.

Competing interests

The author(s) declare that they have no competing interests.

Authors' contributions

The study was designed by HB. SL coordinated the data collection along with the paediatricians. HVB supervised the microbiological testing. SL carried out the data analysis and drafted the manuscript, under the supervision of ER and HB. All co-authors were involved in the interpretation of the data and in the review of the manuscript. All authors read and approved the final version of the manuscript.

Acknowledgements

The study was funded by the Baden-Württemberg state foundation. The foundation was not involved in the study design, collection, analysis, or interpretation of data, writing of the paper, or the decision to submit the paper for publication.

References

  1. Livermore DM: Bacterial resistance: origins, epidemiology, and impact.

    Clin Infect Dis 2003, 36(Suppl 1):S11-23. OpenURL

  2. Cizman M: The use and resistance to antibiotics in the community.

    Int J Antimicrob Agents 2003, 21(4):297-307. OpenURL

  3. German Institute for Standardization (DIN) Medical microbiology - Susceptibility testing of microbial pathogens to antimicrobial agents (Medizinische Mikrobiologie und Immunologie. E 58 940 Part 4 (Methoden zur Empfindlichkeitsprüfung von bakteriellen Krankheitserregern (außer Mykobakterien) gegen Chemotherapeutika) Berlin , Beuth-Verlag;

  4. Sturmer T, Erb A, Marre R, Brenner H: Prevalence and determinants of antibiotic resistance in faecal Escherichia coli among unselected patients attending general practitioners in Southwest Germany.

    Pharmacoepidemiol Drug Saf 2004, 13(5):303-308. OpenURL

  5. London N, Nijsten R, Mertens P, v d Bogaard A, Stobberingh E: Effect of antibiotic therapy on the antibiotic resistance of faecal Escherichia coli in patients attending general practitioners.

    J Antimicrob Chemother 1994, 34(2):239-246. OpenURL

  6. Garau J, Xercavins M, Rodriguez-Carballeira M, Gomez-Vera JR, Coll I, Vidal D, Llovet T, Ruiz-Bremon A: Emergence and dissemination of quinolone-resistant Escherichia coli in the community.

    Antimicrob Agents Chemother 1999, 43(11):2736-2741. OpenURL

  7. Killgore KM, March KL, Guglielmo BJ: Risk factors for community-acquired ciprofloxacin-resistant Escherichia coli urinary tract infection.

    Ann Pharmacother 2004, 38(7-8):1148-1152. OpenURL

  8. Alos JI, Serrano MG, Gomez-Garces JL, Perianes J: Antibiotic resistance of Escherichia coli from community-acquired urinary tract infections in relation to demographic and clinical data.

    Clin Microbiol Infect 2005, 11(3):199-203. OpenURL

  9. Andersen NF, Moller J, Peterslund NA: Piperacillin-resistant Escherichia coli bacteraemia: relation to empiric therapy and clinical outcome.

    Scand J Infect Dis 2005, 37(2):90-95. OpenURL

  10. Edlund C, Nord CE: Effect on the human normal microflora of oral antibiotics for treatment of urinary tract infections.

    J Antimicrob Chemother 2000, 46 Suppl A:41-48. OpenURL

  11. Filius PM, Gyssens IC, Kershof IM, Roovers PJ, Ott A, Vulto AG, Verbrugh HA, Endtz HP: Colonization and resistance dynamics of gram-negative bacteria in patients during and after hospitalization.

    Antimicrob Agents Chemother 2005, 49(7):2879-2886. OpenURL

  12. Jonkers D, Swennen J, London N, Driessen C, Stobberingh E: Influence of cefazolin prophylaxis and hospitalization on the prevalence of antibiotic-resistant bacteria in the faecal flora.

    J Antimicrob Chemother 2002, 49(3):567-571. OpenURL

  13. Rydberg J, Cederberg A: Intrafamilial spreading of Escherichia coli resistant to trimethoprim.

    Scand J Infect Dis 1986, 18(5):457-460. OpenURL

  14. Fornasini M, Reves RR, Murray BE, Morrow AL, Pickering LK: Trimethoprim-resistant Escherichia coli in households of children attending day care centers.

    J Infect Dis 1992, 166(2):326-330. OpenURL

Pre-publication history

The pre-publication history for this paper can be accessed here:

http://www.biomedcentral.com/1471-2334/6/119/prepub