Skip to content

Advertisement

  • Case Report
  • Open Access

Recurrent bilateral Mycobacterium bovis necrotizing epididymitis: a case report

Contributed equally
BMC Research Notes201811:308

https://doi.org/10.1186/s13104-018-3426-2

  • Received: 27 November 2017
  • Accepted: 10 May 2018
  • Published:

Abstract

Background

Mycobacterium bovis causing tuberculosis in animals is responsible for zoonotic tuberculosis in patients. Veterinary control measures and milk pasteurization has led to a significant decrease in human cases of M. bovis infections in developed countries.

Case presentation

We diagnosed recurrent M. bovis epididymitis in a 63-year old Caucasian man without any signs of pulmonary or disseminated disease. Relevant epidemiological expositions included camel milk drinking during prolonged travels in Niger, prior to initial clinical manifestations. The diagnosis was firmly established by mass spectrometry and DNA sequencing on epididymis surgical biopsy specimens. We detail therapeutic management which included surgical epididymectomy and hydrocele repair.

Conclusion

As for other M. tuberculosis complex species, the genitourinary tract represents a frequent site of secondary dissemination and latency for M. bovis. Isolated epididymis infection is a newly documented manifestation of M. bovis disease.

Keywords

  • Mycobacterium bovis
  • Zoonosis
  • Epididymitis

Background

Mycobacterium bovis, a member of the Mycobacterium tuberculosis complex is responsible for bovine-type tuberculosis [1]. Animal to human transmission mainly occurs through airborne route or ingestion of unpasteurized milk. M. bovis attenuated Bacille Calmette-Guérin (BCG) strain vaccination campaigns together with milk pasteurization and better veterinary control measures has led to a decrease in the number of human M. bovis infections [2]. Sporadic cases of human M. bovis suspected zoonotic acquisition are still reported particularly in some developing countries [3]. Also, re-emergence in human populations has been notified in some developed countries still affected by bovine tuberculosis [4].

Mycobacterium tuberculosis complex genitourinary infections represented 6.5% of all extra-pulmonary tuberculosis declared cases in the United States between 1993 and 2006 [5]. Although tuberculous epididymitis is a well described clinical entity, no case has ever been documented with M. bovis as the causative agent [6]. We here report the first such case in a 63-year old man with recurrent bilateral M. bovis granulomatous epididymitis requiring repeated surgical management.

Case presentation

In 2016, a 63-year-old Caucasian French-born retired man was referred to our institution with a 3-month history of left testicular pain and swelling. He was afebrile and in no apparent distress. Detailed clinical evaluation revealed a tender and swollen left epididymis with associated hydrocele but without torsion, focal testicular mass, purulent discharge or pain on digital rectal examination. He was in a long-term exclusive heterosexual relationship and reported no active risk factors or past episodes of sexually transmitted diseases. Standard bacterial urine cultures following prostate massage were sterile. Chlamydia trachomatis and Neisseria gonorrhea polymerase chain reaction assays performed on first-void urine were negative for both him and his sexual partner. Syphilis and HIV serology were also non-reactive.

Past medical history was unrevealing except for a similar episode which had occurred 6 years before and for which a right epididymectomy had been performed. At that time, results of the histological investigation had shown epididymitis with caseo follicular lesion whereas standard bacterial and mycobacterial culture had failed to identify a specific etiology. A surgical left epididymectomy and hydrocele repair was performed and per-operatory examination revealed pachy-vaginalitis and sub-acute epididymitis with multiple caseous purulent collections. Testes were macroscopically normal. On histological examination, necrotizing and granulomatous epididymitis with caseous abscesses were described (Fig. 1) but periodic acid Schiff and Ziehl stainings showed no microorganisms. The patient was therefore empirically treated for sexually transmitted diseases and bacterial epididymitis with initial intravenous ceftriaxone and oral azithromycin followed by a 3-week course of oral ciprofloxacin.
Fig. 1
Fig. 1

Histopathologic findings on surgical biopsy specimens showing necrotic and caseous abscess lesions (left) and peri-arteriolar tropism of necrotizing and fibrinoid inflammation (right)

Three weeks following surgical intervention, mycobacterial liquid medium cultures came back positive. While awaiting final identification and anti-mycobacterial susceptibility testing, a standard anti-tuberculous therapy including isoniazid, rifampin, pyrazinamide and ethambutol was initiated. The isolate was subsequently identified as M. bovis, a mycobacterial species known to be intrinsically resistant to the first-line anti tuberculous drug pyrazinamide [7]. Identification to the species level was confirmed using partial 16S rRNA gene (primer fD1: 5′-AGAGTTTGATCCTGGCTCAG-3′; and primer rP2: 5′-ACGGCTACCTTGTTACG ACTT-3′) and partial rpoB gene (primer MycoF: 5′-GGCAAGGTCACCCCGAAGGG-3′; primer MycoR: 5′-AGCGGCTGCTGGGTGATCATC-3′) sequencing and mass spectrometry per local procedures [8, 9]. Differentiation between this clinical isolate and the attenuated M. bovis BCG strain was confirmed with subsequent multiplex polymerase chain reaction (PCR) assay [10]. Antimycobacterial susceptibility testing showed the isolate to be pan-susceptible to first-line anti-tuberculous drugs other than pyrazinamide and therapy was therefore modified for isoniazid and rifampin alone. Complementary investigation including mycobacterial blood cultures and a whole-body computerized tomodensitometry was also performed and showed no sign of concomitant pulmonary or disseminated disease.

Mycobacterium bovis is a recognized zoonotic disease of which genito-urinary infection presentations are rare. Therefore, potential epidemiologic expositions were further detailed. The patient reported numerous prolonged travels in north and sub Saharan Africa in the 80’s and 90’s. During these stays he was in close contacts with cattle and he regularly ingested camel milk in the Niger desert as Touareg habit. He had never received M. bovis BCG intravesical irrigations or anti-tuberculous vaccine and denied having ever had sexual relations with animals.

The patient stopped antimycobacterial therapy against medical advice 2 weeks after initiation and still refuses to be treated. Upon submission of this manuscript, 1 year after the initial diagnosis, no local relapse had occurred and urine control mycobacterial culture was negative.

Discussions and conclusions

Mycobacterium bovis is a global zoonotic pathogen. Human infections are almost always acquired by ingestion of unpasteurized dairy products or aerosol inhalation from infected animals [2]. Although cattle are the most frequent source of human infections, other farm and wildlife animals have been shown to be susceptible to M. bovis [11]. M. bovis survives in the environment and soil reservoirs were proposed as an hypothesis to explain encountered difficulties in bovine-tuberculosis eradication campaigns [12]. Human to human transmission of M. bovis appears to be anecdotal [13], what raises the unanswered question of relative virulence of M. bovis and M. tuberculosis in human beings.

Despite successful bovine tuberculosis eradication programs and more systematic milk pasteurization, human infections still occur. Surveys from low tuberculosis incidence countries where disease had been eradicated in cattle reported a total of 459 human cases over a 20-year period [11]. Among these, the relative proportion of primary infections and late reactivations can’t be established with precision although it is clear that M. bovis has the ability to enter dormancy and thus persisting for extended periods of time in individuals similarly to other members of the M. tuberculosis complex [14]. This phenomenon could account for this persistent epidemiology in humans. These same surveys estimated that genitourinary infections accounted for 12–53% of human M. bovis infections [11]. Kidney, bladder and urinary tract infections mainly account for this epidemiology. A detailed literature review revealed only one previous suspected case of M. bovis associated scrotal abscess and granulomatous epididymitis [15]. In this previous study, diagnosis was made on the basis compatible epididymis histopathologic findings concomitant with pulmonary cavitary disease and M. bovis positive sputum culture. Although the authors could not confirm the presence of M. bovis by culture or molecular biology in an epididymis specimen, this case presentation is compatible with pulmonary infection and secondary testicular dissemination. Oppositely our patient had no signs of active pulmonary or disseminated disease which argues for epididymis focalized reactivation. Although it could not be confirmed retrospectively by microbiologic or histopathologic analyses, our patient had most likely suffered from contralateral M. bovis epididymitis 6 years prior to the episode here described. At that time, surgical epididymitis was performed and the patient received no anti-tuberculous drug therapy. These elements reinforce the notion that the genitourinary tract is a frequent sanctuary for M. tuberculosis complex bacilli. Table 1 compares the epidemiologic, clinical and therapeutic features of these two discussed cases.
Table 1

Reported Mycobacterium bovis associated epididymitis

 

Age

Sex

Genital disease

Distant infection

Epidemiologic exposition

Treatment

Outcome

Anti-tuberculous therapy

Surgical management

Mateos Colino et al. [15]

73

M

Epididymitis scrotal abscess

Lung cavitary lesion

Cattle

Isoniazid + rifampin 12 months

Scrotal drainage

Chronic fistulation

This case

63

M

Epididymitis hydrocele

None

Camel milk

None (refused by patient)

Epididymectomy scrotal drainage

Ongoing treatment

From the microbiology laboratory perspective, the attenuated form of M. bovis, Bacille Calmette-Guérin (BCG), can be misidentified as wild-type M. bovis using first-line conventional phenotypic and molecular assays. Moreover, M. bovis BCG is still widely used in the treatment of bladder cancer and multiple cases of the genitourinary infections following intravesical therapy have been reported [16, 17]. We identified this M. bovis clinical isolate using mass spectrometry and rpoB gene DNA sequencing [8, 9]. Indeed, alignment of 16S rRNA and rpoB gene sequences yielded the same result with 99% sequence similarity with the reference M. bovis AF2122/97 (GenBank LT708304.1). A two-step, multiplex PCR was also performed to further distinguish between wild-type and attenuated M. bovis strains [10]. All assays were performed in the presence of appropriate controls. Since this organism was identified on surgical biopsy specimens and as no M. bovis isolates were concomitantly handled in our laboratory at the time specimens were obtained, pre-analytic and in-laboratory cross contamination is highly improbable.

In 2016, the United States Centers for Disease Control and Prevention published tuberculosis treatment guidelines [18]. In these recommendations, M. bovis is considered as pyrazinamide mono-resistant M. tuberculosis and therefore justifies a 2-month combination therapy with isoniazid, rifampicin and ethambutol followed by a 7-month course of isoniazid and rifampicin. Also in 2016, Lan et al. [19] published a systematic review on the treatment of human disease due to M. bovis. Despite limited evidence, the authors conclude that the benefit of ethambutol as a third drug in this combination therapy is unclear and that there are no data to support a shorter than 9 months treatment regimen. We interpreted M. bovis as being responsible for this patient’s clinical presentation but the patient refused to complete antimycobacterial therapy despite our recommendations. One year after surgery no local relapse had occured and urine control mycobacterial culture was negative. Surgical management alone should not be considered for M. bovis genitourinary infections. This is reinforced by the fact that our patient most likely relapsed 6 years after an initial episode of epididymitis.

Intensive veterinary, alimentary and public health interventions have significantly reduced the burden of disease associated with M. bovis disease in humans. Nevertheless, infections still occur through airborne and digestive routes. This case is highly interesting since it documents isolated relapsing non-BCG M. bovis epididymitis without concomitant pulmonary or disseminated disease for the first time. M. bovis clinical and microbiological surveillance need to be maintained as this species harbors intrinsic resistance to anti-tuberculous drugs therefore requiring a specific treatment regimen.

Notes

Abbreviations

BCG: 

Bacille Calmette-Guérin

PCR: 

polymerase chain reaction

Declarations

Authors’ contributions

All cited authors qualify for authorship according to the ICMJE guidelines. SGL reviewed patient’s medical chart and microbiology data, performed literature review and was a major contribution in writing the manuscript. SDT was implicated in patient clinical care, chart review and microbiologic investigation, MF performed veterinary literature review and analysis, CE was implicated in patient surgical care, FB performed second line confirmatory molecular testing, CG performed histopathologic interpretation of clinical samples, MD overviewed the microbiological analyses and was a minor contribution in writing the manuscript. All authors read and approved the final manuscript.

Acknowledgements

Not applicable.

Competing interests

The authors declare that they have no competing interests.

Availability of data and materials

Data supporting this manuscript can be accessed via the corresponding author upon reasonable request.

Consent for publication

Written and signed consent to publish the information presented in this manuscript was obtained from the patient.

Ethics approval and consent to participate

Not applicable.

Funding

This work was supported by MEPHI, IHU Méditerranée Infection, Marseille, France.

Publisher’s Note

Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.

Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), 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 (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.

Authors’ Affiliations

(1)
Aix-Marseille Univ, IRD, MEPHI, IHU Méditerranée Infection, 19-21 Boulevard Jean Moulin, 13005 Marseille, France
(2)
Centre Hospitalier Louis Raffalli, 04100 Manosque, France
(3)
Centre Hospitalier du Pays d’Aix, 13616 Aix en Provence, France

References

  1. Domingo M, Vidal E, Marco A. Pathology of bovine tuberculosis. Res Vet Sci. 2014;97(Suppl):S20–9.View ArticlePubMedGoogle Scholar
  2. O’Reilly LM, Daborn CJ. The epidemiology of Mycobacterium bovis infections in animals and man: a review. Tuber Lung Dis. 1995;76(Suppl 1):1–46.View ArticlePubMedGoogle Scholar
  3. Cosivi O, Grange JM, Daborn CJ, Raviglione MC, Fujikura T, Cousins D, Robinson RA, Huchzermeyer HF, de Kantor I, Meslin FX. Zoonotic tuberculosis due to Mycobacterium bovis in developing countries. Emerg Infect Dis. 1998;4(1):59–70.View ArticlePubMedPubMed CentralGoogle Scholar
  4. Thoen CO, LoBue PA. Mycobacterium bovis tuberculosis: forgotten, but not gone. Lancet. 2007;369(9569):1236–8.View ArticlePubMedGoogle Scholar
  5. Peto HM, Pratt RH, Harrington TA, LoBue PA, Armstrong LR. Epidemiology of extrapulmonary tuberculosis in the United States, 1993–2006. Clin Infect Dis. 2009;49(9):1350–7.View ArticlePubMedGoogle Scholar
  6. Heaton ND, Hogan B, Michell M, Thompson P, Yates-Bell AJ. Tuberculous epididymo-orchitis: clinical and ultrasound observations. Br J Urol. 1989;64(3):305–9.View ArticlePubMedGoogle Scholar
  7. American Society for Microbiology. Clinical microbiology procedures handbook, vol. 2. 4th ed. Washington D.C.: American Society for Microbiology; 2016.Google Scholar
  8. Adekambi T, Colson P, Drancourt M. rpoB-based identification of nonpigmented and late-pigmenting rapidly growing mycobacteria. J Clin Microbiol. 2003;41(12):5699–708.View ArticlePubMedPubMed CentralGoogle Scholar
  9. Zingue D, Flaudrops C, Drancourt M. Direct matrix-assisted laser desorption ionisation time-of-flight mass spectrometry identification of mycobacteria from colonies. Eur J Clin Microbiol Infect Dis. 2016;35(12):1983–7.View ArticlePubMedGoogle Scholar
  10. Warren RM, Gey van Pittius NC, Barnard M, Hesseling A, Engelke E, de Kock M, Gutierrez MC, Chege GK, Victor TC, Hoal EG. Differentiation of Mycobacterium tuberculosis complex by PCR amplification of genomic regions of difference. Int J Tuberc Lung Dis. 2006;10(7):818–22.PubMedGoogle Scholar
  11. Grange JM. Mycobacterium bovis infection in human beings. Tuberculosis (Edinb). 2001;81(1–2):71–7.View ArticleGoogle Scholar
  12. Courtenay O, Reilly LA, Sweeney FP, Hibberd V, Bryan S, Ul-Hassan A, Newman C, Macdonald DW, Delahay RJ, Wilson GJ, et al. Is Mycobacterium bovis in the environment important for the persistence of bovine tuberculosis? Biol Lett. 2006;2(3):460–2.View ArticlePubMedPubMed CentralGoogle Scholar
  13. Evans JT, Smith EG, Banerjee A, Smith RM, Dale J, Innes JA, Hunt D, Tweddell A, Wood A, Anderson C, et al. Cluster of human tuberculosis caused by Mycobacterium bovis: evidence for person-to-person transmission in the UK. Lancet. 2007;369(9569):1270–6.View ArticlePubMedGoogle Scholar
  14. Lim A, Eleuterio M, Hutter B, Murugasu-Oei B, Dick T. Oxygen depletion-induced dormancy in Mycobacterium bovis BCG. J Bacteriol. 1999;181(7):2252–6.PubMedPubMed CentralGoogle Scholar
  15. Mateos Colino A, Sousa Escandon MA, Golpe Gomez R, Garcia Figueras R, Perez Valcarcel J, Fernandez MA. Tuberculous epididymitis caused by Mycobacterium bovis. Arch Esp Urol. 2003;56(2):175–8.PubMedGoogle Scholar
  16. Shimura H, Ihara T, Mitsui T, Takeda M. Tuberculous granuloma in the scrotal skin after intravesical Bacillus Calmette-Guerin therapy for bladder cancer: a case report. Urol Case Rep. 2017;11:4–6.View ArticlePubMedPubMed CentralGoogle Scholar
  17. Koizumi T, Nakanishi R, Taue R, Yamaguchi K, Nakatuji H, Kishimoto T, Izaki H, Oka N, Takahashi M, Fukumori T, et al. Case of tuberculous epididymitis caused by intravesical BCG therapy. Hinyokika Kiyo. 2008;54(9):625–7.PubMedGoogle Scholar
  18. Nahid P, Dorman SE, Alipanah N, Barry PM, Brozek JL, Cattamanchi A, Chaisson LH, Chaisson RE, Daley CL, Grzemska M, et al. Official American thoracic society/centers for disease control and prevention/infectious diseases society of America clinical practice guidelines: treatment of drug-susceptible tuberculosis. Clin Infect Dis. 2016;63(7):e147–95.View ArticlePubMedGoogle Scholar
  19. Lan Z, Bastos M, Menzies D. Treatment of human disease due to Mycobacterium bovis: a systematic review. Eur Respir J. 2016;48(5):1500–3.View ArticlePubMedGoogle Scholar

Copyright

© The Author(s) 2018

Advertisement