Skip to main content
  • Research article
  • Open access
  • Published:

Elevated prevalence of multidrug-resistant gram-negative organisms in HIV positive men



Routes of transmission of multidrug-resistant gram-negative organisms (MDRGN) are not completely understood. Since sexual transmission of MDRGN might represent a potential mode that has not been noticed so far, this study evaluated transmission of MDRGN in HIV positive men.


Between November 2014 and March 2016, we retrospectively investigated the MDRGN prevalence in rectal swabs of n = 109 males tested positive for HIV (HP). These findings were compared to the MDRGN prevalence in n = 109 rectal swabs in age-matched males tested negative for HIV (HN) within the same period. According to the infection control protocol of University Hospital Frankfurt, Germany (UHF), patients admitted to intensive/intermediate care units have to be screened for MDRGN on day of admittance. Patients without HIV testing or MDRGN screening were excluded.


MDRGN prevalence in rectal swabs was significantly higher (p = 0.002) in male HP (23.9%; 95% confidence interval 16.2–32.9%) than in age-matched male HN (8.3%; 3.8–15.1%). In total, 35 MDRGN species were detected. The most frequent MDRGN species was Escherichia coli with resistance due to ESBL expression and additional resistance to fluoroquinolones with n = 25/35 (71.4%; 53.7–85.4%). Thereof, n = 19/26 (73.1%; 52.2–88.4%) were detected in HP and n = 6/9 (66.7%; 29.9–92.5%) in HN, respectively.


Prevalence of MDRGN is significantly higher in male HIV positive than in male HIV negative individuals. This might indicate sexual transmission of MDRGN within the male HIV positive population. As treatment options in case of MRGN infections are limited, prevention of MDRGN transmission is strongly emphasized.

Peer Review reports


Multidrug–resistant gram–negative organisms (MDRGN), which have previously been defined as Enterobacteriaceae with extended spectrum beta–lactamase (ESBL)–phenotype, and Enterobacteriaceae, Acinetobacter baumannii and Pseudomonas aeruginosa resistant against piperacillin, any 3rd/4th generation cephalosporin, and fluoroquinolones +/– carbapenems [1], are frequent causes of community and healthcare-associated infections [2, 3]. In recent years, carbapenems became the drugs of choice for the treatment of invasive MDRGN infections [4]. At the same time, the consumption of carbapenems has been increased dramatically [5] and the worldwide prevalence of carbapenemase-producing organisms soon after was found to be elevated [6, 7]. While the explosive spread of carbapenemases has previoulsy been attributed to several factors, such as increasing administration of carbapenems or contact to the health care system in high-prevalence countries (HPC) [810], global spread might also be favored by plasmid encoded resistance genes transfer [11]. However, comprehensive knowledge of the ways of transmission is still lacking. Future concise considerations on the spread of MDRGN should therefore also evaluate routes of transmission that have not been noticed so far. We hypothesize that microbiota, with MDRGN might be part of it, is exchanged during mucous membranes contacts, e.g. sexual intercourse, Although the primary route of MDRGN transmission might be different, sexual transmission should therefore not dismissed. This hypothesis has previously been confirmed by investigations on the sexual transmission of Human Herpes Virus Type 8, E. coli O117:H7 and Shigella spp., although the primary route of these agents’ transmission is via saliva or feco-orally, respectively [1214]. It additionally should be taken into account that it has previously been reported that the risk to acquire “classical” sexually transmitted diseases (STD) such as gonorrhea or syphilis, or infection with the Human Immunodeficiency Virus (HIV) is higher in cohorts of men who have sex with men (MSM) than for the general population [15, 16]. This has also been demonstrated for Germany [17, 18]. With regard to these aspects, pre– or co–existing STD (e.g. HIV infection) have been demonstrated to be suitable parameters to identify individuals with previous or current unprotected, “risky” sexual intercourse. We therefore hypothesize that MDRGN prevalence might be higher in patient groups with HIV infection compared to patient groups tested negative for HIV. In light of the persistent global spread of MDRGN, possibly with a number of different routes, the role of sexual transmission has to be clarified. We present the first study addressing this possible transmissibility of MDRGN by sexual intercourse.


MDRGN screening policy at University Hospital Frankfurt, Germany

According to German infection protection law it is mandatory for hospitals to execute documented infection control strategies to prevent the transmission of infective agents and protect patient health. At University Hospital Frankfurt, Germany (UHF), several defined patient risk groups are screened for MDRGN and methicillin resistant Staphylococcus aureus (MRSA) on day of admittance, such as patients admitted to intensive/intermediate care units (ICU/IMC) at UHF. This means, that each patient will get screened in case of admittance to ICU/IMC at UHF independently from his medical diagnosis.

Patients and specimens

We retrospectively identified and included adult individuals having had both a rectal screening for MDRGN and HIV testing between November 2014 and March 2016. Patients having had only one of the parameters (screening for MDRGN or testing for HIV) were excluded from this study. Patients tested positive for HIV and having had a rectal screening for MDRGN qualified for the case cohort, hereinafter referred to as HP. Vice versa, patients tested negative for HIV and having had a rectal screening for MDRGN qualified for the control cohort, hereinafter referred to as HN.

Identification of cases (HP) and controls (HN) was performed as follows. First, individuals serologically tested positive for HIV and admitted to the department for Internal Medicine II/Infectious Diseases at UHF were identified. Subsequently, these patients were evaluated for being routinely screened for MDRGN during the observation period according to the infection control protocol of UHF. Control patients who were tested serologically negative for HIV and admitted to any department at UHF were also evaluated for being routinely screened for MDRGN during the observation period. Cases and controls were matched on +/- 2 years. By this approach, n = 109 male HP and male HN each qualified for this study. Additionally, digital patient data files were evaluated to stratify patients’ general groups of diseases. Furthermore, the stadium of HIV infection was defined according to CDC criteria [19] of all the patients admitted to the department of Internal Medicine II/Infectious Diseases. With regard to the pilot character of this study and small number of individuals who meet inclusion criteria, co-morbidities and previous antibiotic use were not considered in sampling.

Detection of MDRGN and molecular resistance analysis

The results for the patients’ MDRGN status were retrospectively investigated. For the investigation, we performed a proven methodical procedure that has formerly been published [1]. During the retrospective observation period, all laboratory testing procedures were performed by the Institute for Medical Microbiology and Infection Control at UHF under strict quality–controlled criteria (laboratory accreditation according to ISO 15189:2007 standards; certificate number D–ML–13102–01–00, valid through January 25th, 2021). Rectal swabs were collected using culture swabs with Amies collection and transport medium (Hain Lifescience, Nehren, Germany) and streaked onto selective CHROMagar™ ESBL plates (Mast Diagnostica, Paris, France). Identification of presumed MDRGN species was done by matrix-assisted–laser desorption ionization–time of flight analysis (MALDI–TOF; VITEK MS, bioMérieux, Nürtingen, Germany). Antibiotic susceptibility testing was performed according to Clinical and Laboratory Standards Institute (CLSI) guidelines using VITEK 2 and/or antibiotic gradient tests (bioMérieux) where necessary. In case of gram-negative carbapenem-resistant isolates, detection of genes encoding carbapenemases were routinely performed via PCR analysis and subsequent sequencing from carbapenem resistant Enterobacteriaceae including the bla genes for the following carbapenemases: NDM, VIM, IMP, OXA–48, and KPC [10, 11, 20].

Detection of HIV-1/2 antibodies

Considering that HIV positivity has been suggested to be a marker for a risky sexual behaviour [20], we retrospectively evaluated the HIV status of each individual by examination of the patient files. HIV testing was only performed if medically indicated by physicians at UHF. Laboratory HIV testing was performed by Institute for Medical Virology at UHF under strict quality–controlled criteria (laboratory accreditation according to ISO–15189:2007 standards; certificate number D–ML–13102–03–00 valid through 08.12.2018). All serum samples had been previously screened with the HIV antigen/antibody (Ag/Ab) Combo Screening Assay (Abbott, Delkenheim, Germany; Architect System; REF 4 J27) working with the Architect system detecting HIV–1/2 antibodies and HIV–1 p24 antigen. Samples with reactive screening assay results (positive, indeterminate) were further evaluated using the western blot New Bio-Rad LAV–Blot I and LAV–Blot II (Bio–Rad Laboratories GmbH, München, Germany), which uses native HIV proteins. The assay was performed as outlined in guidelines provided by the manufacturer.

Statistical analysis

Sample size of n = 109 individuals per group proved to be adequate by a power = 0.95 and Cohen’s d = 0.5. Chi squared test was performed for statistical analysis. 95% confidence intervals (95% CI) for frequencies were calculated based on binomial distribution and used to confirm statistical significance. P-values ≤ 0.05 were considered as statistically significant.


In the current study, we evaluated n = 109 male HP and n = 109 male HN, respectively, admitted to UHF between November 2014 and March 2016. Both the male HPs’ and male HNs’ median age was 46 years, the standard deviation being 10.8 and 11.0 years, respectively.

Table 1 shows the general groups of diseases HP and HN they were admitted for to UHF. In HP, the most frequent group were patients admitted to the department of Internal Medicine II/Infectious Diseases with 82.6% (n = 90/109). HN were most frequently admitted to UHF due to oncological diseases with 39.4% (n = 43/109). Among male HP and male HN, a total of n = 35 MDRGN isolates were detected. Thereof, n = 26/109 and n = 9/109 rectal swabs were positive for any MDRGN in male HP and male HN, respectively, which resulted in an overall MDRGN prevalence of 23.9% (16.2–32.9) in male HP and a significantly (p = 0.002) lower MDRGN prevalence in male HN with 8.3% (3.8–15.1). Looking into the single proportions of the detected MDRGN, no significant differences were detected between male HP and HN patients, respectively (Fig. 1).

Table 1 General group of diseases HIV positive (HP) patients and HIV negative (HN) patients were admitted for to University Hospital Frankfurt, Germany (UHF), as given by the digital patient data files
Fig. 1
figure 1

Prevalence (%) of multidrug-resistant gram-negative organisms (MDRGN) in patients tested positive (HP) and negative for HIV (HN). 95% confidence intervals are marked as ranges; percentage and 95% confidence intervals are given

The most frequently detected species within the MDRGN isolates (n = 35 in total) was E. coli with resistance due to ESBL expression and additional resistance to fluoroquinolones (E. coli ESBL/FQ) with n = 25/35 (71.4%; 53.7–85.3). Thereof, E. coli ESBL/FQ was detected in n = 19/26 (73.1%; 52.2–88.4%) of male HP and in n = 6/9 (66.7%; 29.9–92.5%) of male HN (p = 0.713), respectively. All MDRGN detected in male HP and male HN are depicted by in Table 2. None of the bacterial species P. aeruginosa or A. baumannii and neither, no resistance to carbapenems were detected in any of the isolates from male HN nor any of HP.

Table 2 Prevalence of multidrug-resistant gram-negative organisms in males tested positive for HIV and males tested negative for HIV


In light of the explosive global spread of MDRGN, attention must be directed to potential routes of transmission that have not been recognized so far. Several routes of transmission, e.g. traveling in HPC [8], antibiotic selective pressure [5], or transmission by livestock [21] have previously been demonstrated. However, to our knowledge this is the first study focusing on the potential transmission of MDRGN in male HIV positive individuals.

The prevalence of MDRGN in male HN amounted to 8.3% (3.8–15.1; Table 2). This value does not substantially deviate from the prevalence of ESBL of about 6.3% in clinical specimen, which has formerly been described to be 6.3% by a German cross–sectional study [22]. However, the prevalence of MDRGN in rectal swabs of male HP (23.9%; 16.2–32.9) exceeded the value investigated by Valenza et al. [22] by almost three-fold. These findings suggest that HIV positive men might be more susceptible to acquire MDRGN. Furthermore, our findings indicate a pre–dominance of E. coli ESBL/FQ (Table 1), it might therefore be interesting to characterize these E. coli-isolates isolated from male HP further for expression of pathogenicity factors, e.g. type 1 fimbriae (fimH), pili associated with pyelonephritis (pap), S and F1C fimbriae (sfa and foc), afimbrial adhesins (afa), cytotoxic necrotizing factor (cnf), hemolysin (hly) or aerobactin (aer) using molecular techniques [23] and subsequently compare these findings with isolates collected from HN. We therefore feel it is warranted to further characterize MDRGN isolates isolated from HP and HN by molecularbiological methods, preferentially by whole genome sequencing (WGS).

Although no significant differences in proportion of any single MDRGN species were observed (Table 2), this might indicate that the sexual route of transmission is apparently not preferred by any particular MDRGN species. It rather might be interpreted as a general inherent risk to acquire a MDRGN. Since the sexual route of transmission of MDRGN has not been suggested so far, this is as important finding of this study. However, several epidemiological events give an impression that sexual spread of organisms is possible, although their preferred way of transmission is reported to be non-sexual: Shigella sonnei, which is either none of the “classical” STD-causing organisms, has been shown to spread among men who have sex with men (MSM) in Montréal, Canada, and Germany [24, 25] the verocytotoxin-producing EHEC O117:H7 has also been documented to spread among MSM in Great Britain [16] and, as well, no “classical” STD, meningococcal serogroup C diseases has newly been shown to spread among MSM [26, 27]. This outlines that sexual transmission of Enterobacteriaceae is distinctly possible via translocation of intestinal bacteria. Sexual transmission of MDRGN is therefore suggested not to be dismissed in future comprehensive considerations on MDRGN transmission prevention.

However, the link between HIV positivity and risky sexual behavior must be interpreted diligently: if positive HIV serology might indicate that the patient has previously had a risky behavior (and HIV was not contracted e.g. by blood transfusion), this may have lasted for years up to now, or it may have ended in the meanwhile. The time of carriage of MDRGN might be short [28] and we therefore cannot ascertain that the timeframes between the risky behavior and MDRGN acquisition could coincide. However, at this time we did not see any alternative assessment available to clarify the potential route of sexual transmission.

Concerning that data regarding the history of previous hospital stays nor antibiotic pre–treatment for male HP and male HN were not evaluated, it is not possible to confirm that male HP in the UHF–setting might have had a stronger history of antibiotic pre–treatment than male HN. Considering that all patients enrolled in this investigation matched the requirement to be screened for MDRGN (which is usually limited to patients admitted to ICU or IMC at UHF), this might indicate that both male HP and male HN had a recent history of antibiotic treatment. However, HIV patients in particular might have undergone a prexisiting antibiotic pressure due to their HIV infection (e.g. administration of cotrimoxazole to treat Pneumocystis jirovecii pneumonia) and might therefore have a higher risk for admittance to hospitals and health care facilities where nosocomial MDRGN transmissions can occur [29]. These aspects might therefore have introduced a source of biases in the selection of patients.

However, not also antibiotic treatment, but also pre–existing co-morbidities also might be an aspect that has to be evaluated in a future setting to round off investigations on conditions of sexual transmission of MDRGN. Since gastrointestinal diseases or co-infections might compromise the gastrointestinal mucosa, this might promote the transmission of MDRGN. As such interrelation has formerly been shown for amebiasis and HIV [30], this aspect should not be neglected.

Furthermore, it remains open to question whether these findings are also valid for women. As urinary tract infections (UTI) are one of the most common (usually endogenous) bacterial infections often triggered by sexual intercourse, and many women suffer from at least one UTI during their lifetime [31], in a future setting the prevalence of MDRGN should be investigated in urogenital and/or vaginal swabs in female cohorts.


Our study demonstrated that prevalence of MDRGN in HIV positive male individuals is significantly higher than in HIV negative male individuals. Although no significant differences in proportion of any single MDRGN species were observed, this indicates that sexual transmission of MDRGN within the male HIV positive population is possible. With regard to the results of this study, practicing safer sex should be propagated actively further on to reduce not only the spread of many STD-associated pathogens but most likely also MDRGN.



Confidence interval


Clinical and Laboratory Standards Institute


Enterohaemorrhagic Escherichia coli


Extended spectrum beta–lactamase


ESBL expression and additional resistance to fluoroquinolones


Human immunodeficiency virus


Males serologically tested negative for HIV


Males serologically tested positive for HIV


High-prevalence countries


Intensive care unit


Intermediate care unit


Imipenem-hydrolyzing beta-lactamase


Klebsiella pneumoniae carbapenemase


Mass-assisted–laser desorption ionization–time of flight analysis


Multidrug-resistant gram-negative organisms


Men who have sex with men


New Delhi metallo-beta-lactamase


Polymerase chain reaction


Sexually transmitted diseases


University Hospital Frankfurt, Germany


Urinary tract infection


Verona integron-encoded metallo-beta-lactamase


Whole genome sequencing


  1. Reinheimer C, Kempf VA, Göttig S, Hogardt M, Wichelhaus TA, O’Rourke F, Brandt C. Multidrug-resistant organisms detected in refugee patients admitted to a University Hospital, Germany June–December 2015. Euro Surveill. 2016;21(2). doi: 10.2807/1560-7917.ES.2016.21.2.30110.

  2. Magiorakos AP, Srinivasan A, Carey RB, Carmeli Y, Falagas ME, Giske CG, et al. Multidrug-resistant, extensively drug-resistant and pandrug-resistant bacteria: an international expert proposal for interim standard definitions for acquired resistance. Clin Microbiol Infect. 2012;18:268–81. doi:10.1111/j.1469-0691.2011.03570.

    Article  CAS  PubMed  Google Scholar 

  3. Rossolini GM, D’Andrea MM, Mugnaioli C. The spread of CTX-M-type extended- spectrum beta-lactamases. Clin Microbiol Infect. 2008;14 Suppl 1:33–41. Review. Erratum in: Clin Microbiol Infect. 2008 May;14 Suppl 5:21-4.

    Article  CAS  PubMed  Google Scholar 

  4. Paterson DL, Bonomo RA. Extended-spectrum β-lactamases: a clinical update. Clin Microbiol Rev. 2005;18:657–86.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  5. Van Boeckel TP, Gandra S, Ashok A, Caudron Q, Grenfell BT, Levin SA, et al. Global antibiotic consumption 2000 to 2010: an analysis of national pharmaceutical sales data. Lancet Infect Dis. 2014;14:742–50. doi:10.1016/S1473-3099(14)70780-7.

    Article  PubMed  Google Scholar 

  6. Nordmann P, Naas T, Poirel L. Global spread of Carbapenemase producing Enterobacteriaceae. Emerg Infect Dis. 2011;17:1791–8. doi:10.3201/eid1710.110655.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  7. Rodríguez-Baño J. Carbapenems for ESBL-producing Enterobacteriaceae: The times they are a-changin’. Antimicrob Agents Chemother. 2015;59(9):5095–6. doi:10.1128/AAC.01333-15.

    Article  PubMed  PubMed Central  Google Scholar 

  8. Izdebski R, Bojarska K, Baraniak A, Literacka E, Herda M, Żabicka D, et al. NDM-1- or OXA-48-producing Enterobacteriaceae colonizing Polish tourists following a terrorist attack in Tunis, March 2015. Euro Surveill. 2015; 20. DOI: 10.2807/1560-7917.ES2015.20.23.21150.

  9. Mathers AJ, Hazen KC, Carroll J, Yeh AJ, Cox HL, Bonomo RA, et al. First clinical cases of OXA-48-producing carbapenem-resistant Klebsiella pneumoniae in the United States: the “menace” arrives in the new world. J Clin Microbiol. 2013;51:680–3. doi:10.1128/JCM.02580-12. Erratum in: J Clin Microbiol. 2013;51(4):1352.

    Article  PubMed  PubMed Central  Google Scholar 

  10. Gruber TM, Göttig S, Mark L, Christ S, Kempf VA, Wichelhaus TA, Hamprecht A. Pathogenicity of pan-drug-resistant Serratia marcescens harbouring blaNDM-1. J Antimicrob Chemother. 2015;70(4):1026–30. doi:10.1093/jac/dku482.

    CAS  PubMed  Google Scholar 

  11. Göttig S, Gruber TM, Stecher B, Wichelhaus TA, Kempf VA. In vivo horizontal gene transfer of the carbapenemase OXA-48 during a nosocomial outbreak. Clin Infect Dis. 2015;60(12):1808–15. doi:10.1093/cid/civ191.PMID. 25759432.

    Article  PubMed  Google Scholar 

  12. Reinheimer C, Allwinn R, Stürmer M. Do fewer cases of Kaposi’s sarcoma in HIV-infected patients reflect a decrease in HHV8 seroprevalence? Med Microbiol Immunol. 2011;200(3):161–4. doi:10.1007/s00430-011-0187-0.

    Article  PubMed  Google Scholar 

  13. Simms I, Gilbart VL, Byrne L, Jenkins C, Adak GK, Hughes G et al. Identification of verocytotoxin-producing Escherichia coli O117:H7 in men who have sex with men, England, November 2013 to August 2014. Euro Surveill. 2014;19(43).

  14. Simms I, Field N, Jenkins C, Childs T, Gilbart VL, Dallman TJ et al. Intensified shigellosis epidemic associated with sexual transmission in men who have sex with men-Shigella flexneri and S. sonnei in England, 2004 to end of February 2015. Euro Surveill. 2015;20(15).

  15. Erens B, Phelps A, Clifton S, Mercer CH, Tanton C, et al. Methodology of the third British National Survey of Sexual Attitudes and Lifestyles (Natsal-3) Sexually transmitted infections. 2014;90(2):84–9. doi: 10.1136/sextrans-2013-051359.

  16. Brewer TH, Peterman TA, Hewman DR, Schmitt K. Reinfections during the Florida syphilis epidemic, 2000-2008. Sex Transm Dis. 2011;38(1):12e7. doi:10.1097/OLQ.0b013e3181e9afc7.

    Article  Google Scholar 

  17. Epidemiologisches Bulletin 50/2014, Robert Koch-Institut, Berlin, Germany, Accessed 5 Mar 2017.

  18. Epidemiologisches Bulletin 26/2014, Robert Koch-Institut, Berlin, Germany, Accessed 5 Mar 2017.

  19. Accessed 5 Mar 2017.

  20. Doyle D, Peirano G, Lascols C, Lloyd T, Church DL, Pitout JD. Laboratory detection of Enterobacteriaceae that produce carbapenemases. J Clin Microbiol. 2012;50:3877–80. doi:10.1128/JCM.02117-12PMID. 22993175.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  21. Ghodousi A, Bonura C, Di Noto AM, Mammina C. Extended-spectrum ß-lactamase, AmpC-producing, and fluoroquinolone-resistant Escherichia coli in retail broiler chicken meat, Italy. Foodborne Pathog Dis. 2015;12(7):619–25. doi:10.1089/fpd.2015.1936.

    Article  CAS  PubMed  Google Scholar 

  22. Valenza G, Nickel S, Pfeifer Y, Eller C, Krupa E, Lehner-Reindl V, et al. Extended- spectrum-β-lactamase-producing Escherichia coli as intestinal colonizers in the German community. Antimicrob Agents Chemother. 2014;58(2):1228–30. doi:10.1128/AAC.01993-13.

    Article  PubMed  PubMed Central  Google Scholar 

  23. Yun KW, Kim HY, Park HK, Kim W, Lim IS. Virulence factors of uropathogenic Escherichia coli of urinary tract infections and asymptomatic bacteriuria in children. J Microbiol Immunol Infect. 2014;47:455–61. doi:10.1016/j.jmii.2013.07.010.

    Article  CAS  PubMed  Google Scholar 

  24. Gaudreau C, Ratnayake R, Pilon PA, Gagnon S, Roger M, Lévesque S. Ciprofloxacin-resistant Shigella sonnei among men who have sex with men, Canada, 2010. Emerg Infect Dis. 2011;17:1747–50. doi:10.3201/eid1709.102034.

    Article  PubMed  PubMed Central  Google Scholar 

  25. Hoffmann C, Sahly H, Jessen A, Ingiliz P, Stellbrink HJ, Neifer S, et al. High rates of quinolone-resistant strains of Shigella sonnei in HIV-infected MSM. Infection. 2013;41(5):999–1003. doi:10.1007/s15010-013-0501-4.

    Article  CAS  PubMed  Google Scholar 

  26. Koch J, Hellenbrand W, Schink S, Wichmann O, Carganico A, Drewes J et al. Evaluation of a temporary vaccination recommendation in response to an outbreak of invasive meningococcal serogroup C disease in men who have sex with men in Berlin, 2013-2014. Euro Surveill. 2016;21(5). doi: 10.2807/1560-7917.ES.2016.21.5.30122.

  27. Hellenbrand W, Claus H, Schink S, Marcus U, Wichmann O, Vogel U. Risk of invasive meningococcal disease in men who have sex with men: lessons learned from an outbreak in Germany, 2012-2013. PLoS One. 2016;11(8):e0160126. doi:10.1371/journal.pone.0160126. PMID: 27486669.

    Article  PubMed  PubMed Central  Google Scholar 

  28. Ruppé E, Armand-Lefèvre L, Estellat C, Consigny PH, El Mniai A, Boussadia Y, et al. High rate of acquisition but short duration of carriage of multidrug-resistant Enterobacteriaceae after travel to the tropics. Clin Infect Dis. 2015;61(4):593–600. doi:10.1093/cid/civ333.

    Article  PubMed  Google Scholar 

  29. Stephan C, Just-Nübling G, Franck S, Bickel M, Shah PM, Babacan E, et al. No obvious difference in Streptococcus pneumoniae antibiotic resistance profiles--isolates from HIV-positive and HIV-negative patients. Med Klin. 2008;103:69–74.

    Article  Google Scholar 

  30. Nagata N, Shimbo T, Akiyama J, Nakashima R, Nishimura S, Yada T, et al. Risk factors for intestinal invasive amebiasis in Japan, 2003-2009. Emerg Infect Dis. 2012;18(5):717–24. doi:10.3201/eid1805.111275.

    Article  PubMed  PubMed Central  Google Scholar 

  31. Burleigh AE, Benck SM, McAchran SE, Reed JD, Krueger CG, Hopkins WJ. Consumption of sweetend, dried cranberries may reduce urinary tract infection incidence in susceptible women – a modified observational study. Nutr J. 2013;12(1):139. doi:10.1186/1475-2891-12-139.

    Article  PubMed  PubMed Central  Google Scholar 

Download references


Authors would like to thank all the patients whose samples and data were used for our study.

Authors declare that this report is exclusively based on epidemiological findings and is not influenced by any political opinion. Authors furthermore confirm that all patients are treated equally and in conditions of best medical care at University Hospital Frankfurt, Germany.


Volkhard A. J. Kempf was supported by a grant from the Deutsche Forschungsgemeinschaft (DFG- research unit 2251).

Availability of data and material

All data generated or analysed during this study are included in this published article.

Authors’ contributions

CR: microbiological diagnostics, initiation of the study, compiling data, interpretation of data, writing the manuscript. OTK: hiv diagnostics, compiling data, critical review of the manuscript. CS: compiling data (patient related information), critical review of the manuscript. TAW: microbiological diagnostics, compiling data, critical review of the manuscript. IF: hiv diagnostics, compiling data. VAJK: microbiological diagnostic, compiling data, critical review of the manuscript. All authors agreed to be accountable for all aspects of the word and approved the final version of the manuscript.

Competing interests

The authors declare that they have no competing interests.

Consent for publication

Not applicable.

Ethics approval and consent to participate

Based on the analysis of retrospective data and with regard to §15 Hessian Medical Association’s Professional Code of Conduct (“Berufsordnung für in Hessen tätige Ärzte/innen”), this study was approved by the Ethics Board of the Goethe University Hospital on November 30th, 2015.

Author information

Authors and Affiliations


Corresponding author

Correspondence to Claudia Reinheimer.

Rights and permissions

Open Access This article is distributed under the terms of the Creative Commons Attribution 4.0 International License (, which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver ( applies to the data made available in this article, unless otherwise stated.

Reprints and permissions

About this article

Check for updates. Verify currency and authenticity via CrossMark

Cite this article

Reinheimer, C., Keppler, O.T., Stephan, C. et al. Elevated prevalence of multidrug-resistant gram-negative organisms in HIV positive men. BMC Infect Dis 17, 206 (2017).

Download citation

  • Received:

  • Accepted:

  • Published:

  • DOI: