Running Head
LCMV maintenance in mice over 24 years
ABSTRACT
Lymphocytic choriomeningitis virus (LCMV) is a neglected rodent-borne
zoonotic virus primarily infecting house mice. The virus can be highly
pathogenic, particularly in immunocompromised individuals and in
congenital infections. LCMV is distributed worldwide but shows local
clustering, probably due to the highly structured populations of its
hosts and the vertical transmission of the pathogen. These factors
should also promote long-term virus persistence in wild populations, yet
this aspect remains largely unexplored. To investigate this, we
resampled a transect in the western Czech Republic that was primarily
studied more than a decade ago. Additionally, we analyzed a sample
collection from Buškovice, a locality where LCMV was first detected in
2008, to trace virus presence back to the year 2000. Positive samples
underwent whole-genome characterization to assess the virus’s genetic
structure over space and time. We detected intermittent presence over 24
years in a geographically limited area, where LCMV was already present
in 2000 and remained detectable in 2023. Phylogenetic analysis showed no
clear spatio-temporal clustering, suggesting that virus persistence in
Buškovice is a dynamic process involving mouse dispersal between
neighboring villages. Given LCMV’s zoonotic potential and house mouse
synanthropy, these findings highlight the need for continuous monitoring
in the region.
1. INTRODUCTION
Lymphocytic choriomeningitis virus (LCMV) is a rodent-borne virus with
cosmopolitan distribution due to its primary reservoir host, the house
mouse (Mus musculus ) (1). Other wild rodents (2,3) or
domesticated and pet animals can also serve as reservoirs (4,5). Humans
can become infected after contact with rodent secreta or excreta or by
inhalation of aerosolized particles. Human-to-human transmission has
been documented during transplantation or vertically during intrauterine
development (4,6). In healthy people, the infection is usually
asymptomatic or with mild symptoms. However, in immunocompromised
individuals, the infection can develop into life-threatening conditions,
e.g., aseptic meningitis, encephalopathy or encephalitis. Congenital
infection can lead to miscarriage or severe defects in the fetus, often
of neurodevelopmental manifestation (6).
LCMV is an enveloped RNA virus belonging to the genusMammarenavirus , family Arenaviridae (1). The genome,
approximately 10.6 kb long, consists of two segments: The large (L)
segment carries the RNA-dependent RNA polymerase (L) gene and the RING
finger protein (Z) gene whereas the small (S) segment carries the viral
glycoprotein precursor (GPC) gene and the nucleoprotein (NP) gene.
In natural house mouse populations, LCMV can be transmitted both
horizontally and vertically. When transmitted horizontally, infected
individuals typically mount an immune response that clears the
infection. However, when transmitted vertically, i.e., when mice are
infected with LCMV during the intrauterine period or early in life, they
fail to develop an effective immune response, resulting in a chronic,
asymptomatic, lifelong infection and the agent again can be transmitted
vertically to their offspring which in turn become chronically infected
(5,7). LCMV infections in natural mouse populations have been shown to
be patchy at local and regional scales (5). This pattern was observed in
a recent study in Central Europe, where two subspecies of the house
mouse, Mus musculus musculus and M. m. domesticus, come
into contact and form a narrow hybrid zone ((8); see Figure 1A). After
serological and molecular screening of more than 700 mice sampled
between 2008 and 2014, LCMV was detected in only four localities within
a 12 km² area in the musculus territory in the Czech Republic. In
one locality, Buškovice, LCMV was detected in 2008 and 2014, suggesting
that the virus could persist in this area for several years.
House mouse populations form small, stable and relatively isolated
communities known as “demes” (9,10). This population structure
combined with the vertical transmission of LCMV should favor the focal
spread of the virus (5) but also its long-term persistence within
affected areas. The maintenance of LCMV in natural mouse populations has
been understudied, although this is a key factor in understanding the
dynamics of the virus in reservoir populations and the risk to humans.
The aim of this study was therefore to investigate the focal and
long-term maintenance of the virus in this region and to assess its
genetic structure in space and time.
2. MATERIALS AND METHODS
2.1. Sample collection and LCMV detection
In 2022, 216 house mice from 54 localities in the region between
north-eastern Bavaria (Germany) and western Bohemia (Czech Republic)
were sampled as in (8) and tested for LCMV antibodies (Figure 1B,
Table). As LCMV can also infect other rodent species (2,3,5), 89 small
mammals other than house mice (see Table) but living in sympatry with
them, were also tested for LCMV antibodies. Two additional mice were
sampled in Buškovice in 2023 and included in the screening. The serum of
these individuals was tested with the ELISA kit IM-698 C-EB (XpressBio,
https://xpressbio.com). Of these 218 house mice, 98 individuals, either
from Buškovice or from localities within a 21 km radius of Buškovice,
were further analysed for the presence of LCMV RNA in lung tissue. RNA
was extracted using the RNeasy kit (Qiagen) and subjected to one-step
RT-PCR (Invitrogen SuperScript IV System, ThermoFisher Scientific)
targeting a 340-nucleotide fragment of the L gene (12), following (8).
To go back in time and extend the period for assessing the long-term
maintenance of LCMV in Buškovice, 60 individuals were tested from a -80
°C frozen collection of kidney/lung tissue from house mice sampled in
2000, 2003, 2004, 2008 and 2014 (Table). The molecular one-step RT-PCR
screening was performed as described above.
2.2. Whole genome sequencing and phylogenetic analyses
Five LCMV-positive samples were selected for whole genome sequencing:
JPC2844 from 2000, ST5763 and ST5769 from 2003, SK2670 from 2014 and
JHZ22_002 from 2022. The xGenTM Broad-range RNA Lib
Prep Kit (Integrated DNA Technology) was used for library preparation
and pooled libraries were sequenced with 150 paired-end reads on a
DNBSEQ-G400 at BGI Genomics (Poland). Mouse reads were removed after
mapping against the GRCm39 mouse reference genome using BWA. Unmapped
reads were trimmed and de novo assembled with metaSPAdes (13) and
scaffolds classified using BlobTools (14). The metaSPAdes scaffolds were
then polished by mapping reads to the scaffolds with a consensus
threshold of 60% using Geneious mapper (Geneious,
https://www.geneious.com) to obtain complete LCMV L and S segments. The
L, NP and GPC gene sequences of the newly characterized strains were
aligned with the sequences of LCMV strains SK1194 and SK1042 originating
from two localities eight and four kilometers from Buškovice (see (8)
and Appendix Figure) and with the Dandenong strain originating from the
former Yugoslavia (16). Bayesian phylogenetic analysis was performed in
MrBayes 3.2.7 (15) using the GTR model with gamma rates for all three
genes. Pasteur and Armstrong strains from Clade I sensu Albariño et al.
(2010) (16) were used as outgroups.
3. RESULTS
3.1. Virus detection
The serological screening revealed that LCMV was present in only one of
216 house mice sampled in the region between north-eastern Bavaria and
western Bohemia in 2022. The positive sample came from the subspeciesmusculus from the locality Buškovice. In addition, one of the two
mice from the same locality sampled in 2023 was also positive. LCMV
antibodies were not detected in any of the 89 rodent individuals found
in sympatry with the house mice which included 48 individuals of the
genus Apodemus (Table). Apodemus sylvaticus has been shown
to be a reservoir for LCMV in Spain and Germany (2,3). RT-PCR screening
of the 98 samples centered around Buškovice revealed one additionalmusculus individual positive for LCMV RNA and originating from
Buškovice 2022 (Table, Appendix Table).
RT-PCR screening of older samples from our tissue collection from
Buškovice revealed five positive samples for LCMV RNA: 1 of 2 samples
from 2000, 3 of 16 samples from 2003, and 1 of 7 samples from 2014 were
positive (Table). An overview of the years in which LCMV-positive
individuals were found in Buškovice, either by serological or molecular
screening, and combining the data from Fornuskova et al. (8) and this
study is shown in Figure 2. LCMV was detected in six of the eight years
for which we had samples available (no LCMV was found in 2004 and 2019),
in a total period of 24 years.
3.2. Sequence and phylogeny analyses
Whole genome sequencing of five LCMV strains was successful and allowed
us to assemble their complete genomes. All strains had unique S and L
sequences, but with limited diversity: the average pairwise
nucleotide/amino acid identity was 96.5%/99.6% for the NP gene,
95.3%/97.9% for the GPC gene and 94.6%/96.7% for the L gene. The
topologies of the phylogenetic trees were similar for all three genes
(Figure 3), suggesting the absence of recombination within the S segment
or reassortment between the S and L segments. The five newly
characterized strains clustered with the two LCMV strains previously
characterized in this region, . The tree topologies did not showed a
clear temporal or spatial clustering of samples. The samples are not all
descendant from a single viral lineage for the whole period of 24 years.
Instead, the samples were divided into two temporal clusters, 2000 –
2003 and 2014 – 2022, suggesting that the LCMV lineage present in
Buškovice in 2000 was replaced between 2003 and 2014 by a lineage also
present in the nearby village of Nepomyšl in 2009.
4. DISCUSSIONS
We investigated the spatial clustering and the long-term maintenance of
LCMV in wild house mouse populations in Central Europe, where the two
subspecies known to be natural reservoirs of the virus meet. There, LCMV
was found more than a decade ago in four localities, Nepomyšl, Kryry,
Žihle, and Buškovice, within 12 km2 (8). Our study,
based on samples from 216 mice captured in 2022 (along with two
additional samples from 2023), reinforces the previous finding, with the
virus detected exclusively in the musculus territory. During this
sampling, we did not catch any mice in Nepomyšl and Kryry so it was not
possible to determine whether the virus is still present in these
localities or not. However, samples from Žihle were all negative and we
did not detect LCMV in other localities surrounding Buškovice, which
confirms the LCMV presence is still very limited in space. This focal
distribution has already been reported both locally and on a large
scale. In Baltimore, United States, LCMV infection was shown to vary
drastically between neighboring houses in the same block (18). At the
regional scale, a serological study carried out in West Germany from
1960 to 1962 showed that 65/1795 positive mice were mainly localized in
the regions of North Rhine-Westphalia and southern Lower Saxony (19). In
other regions, no or only a few localities were found positive for LCMV,
with no positive localities in Bavaria.
The detection of the virus in Buškovice in 2023, i.e., 15 years after
the first detection (8), prompted us to investigate whether the virus
was already present in this locality before 2008 by analyzing an old
tissue collection. We detected LCMV in 2000, the earliest sample
available in our collection. Overall, the virus was detected in six out
of eight time points over a 24-year period, either by detection of viral
RNA or using antibodies. Although LCMV was not detected in Buškovice in
2009, it was present in neighboring localities in the same year
(Nepomyšl and Kryry) and in 2010 (Žihle) (8). The maintenance of the
virus from generation to generation in captive house mice has been known
for a long time due to the vertical transmission of the virus (5).
However, data on the long-term maintenance of LCMV in wild mice are
rare. To our knowledge, until our study, the longest LCMV presence in
nature was evidenced in a serological study of wild rodents in northern
Italy, which showed that the prevalence of LCMV in Apodemus
flavicollis fluctuated considerably over a 7-year period (20). The
discontinuous detection in Buškovice is to be expected due to the very
low LCMV prevalence in this region - 2.4% and 0.8% in serological and
molecular assays, respectively (8) - and the limited number of mice
captured in each locality.
The patchy occurrence of LCMV and its long-term maintenance may be due
to the combination of the house mouse population structure and the
vertical transmission of the virus (5). House mice form relatively
stable demes with low dispersal ability (10, 17). Therefore, a deme that
initially acquires an LCMV through horizontal transmission could easily
maintain the virus over many generations by vertical transmission within
the deme. The turn-over of the viral lineage observed between 2003 and
2022 suggests that, despite the strong genetic structure, dispersal of
individuals between adjacent populations occurs and is sufficient to
exchange the virus between neighboring villages.
5. CONCLUSIONS
This study confirms the focal occurrence of LCMV in the sampled region
and reports its persistence in wild mouse populations over a period of
24 years. Thus, human exposure to this zoonotic virus is geographically
limited but persistent over time. This has important implications for
public health and pest control strategies. Targeted measures in a few
localities could potentially eradicate the mouse demes that sustain
LCMV, and thus reduce the risk of transmission to humans. The ability of
the virus to persist in mouse populations over time emphasizes the need
for continuous surveillance to protect public health and prevent
spillover.