Recurrent bilateral Mycobacterium bovis necrotizing epididymitis: a case report

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.

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.

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.

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.

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.